Heparan Sulfate Proteoglycans Mediate In Vitro Human Neuronal Lineage Specification

1. Introduction

Adult neurogenesis is initiated by neural stem cells (NSCs) in selective neurogenic niches within the mammalian brain [1]. NSCs are the most primitive cell type in the central nervous system capable of self-renewal and responsible for the generation of mature neural cell types, including neurons, astrocytes and oligodendrocytes [2]. As NSCs undergo neurogenesis, they progress through numerous stages, including the transition into radial glial cells and neural progenitor cells (NPCs) and then mature into neuron, astrocyte, or oligodendrocyte lineages. Throughout each stage of neurogenesis, distinct progenitor cell types can be identified by specific and often overlapping marker expression profiles [3,4,5]. While neurogenesis has been extensively studied to elucidate the mechanisms of neuronal differentiation, the development and characterisation of astrocyte models remain relatively underexplored. Given the growing recognition of dysfunctional astrocytes in the pathogenesis of neurodegenerative diseases [6], it is critical to establish robust and reproducible astrocyte cell models. However, significant challenges persist in understanding the molecular cues and environmental conditions that drive NPCs toward a glial fate. As a result, the efficient and reliable generation of functional astrocytes in vitro continues to be a complex and unresolved task. This is likely as a result of much of what is known about human neurogenesis has been extrapolated from rodent studies [7], with species-specific differences hindering the translation of findings into human cells. Thus, a more comprehensive understanding of the regulatory mechanisms governing human NPCs, along with their marker profiles during astrocyte lineage specification and subsequent differentiation, is essential for understanding and recapitulating both normal and pathological glial functions.

Adult neurogenesis occurs in two discrete neurogenic niches within the brain, the subventricular zone (SVZ) and the subgranular zone (SGZ) [8]. Heparan sulfate proteoglycans (HSPGs), including the cell surface-bound syndecans (SDCs) and glypicans (GPCs), are ubiquitously expressed macromolecules and major constituents of the NSC niche [9]. Within the neurogenic niches, HSPGs interact with numerous signalling molecules via their highly diverse HS glycosaminoglycan (GAG) side chains. GAGs possess structural complexity mainly due to their highly variable sulfation pattern, a result of a complex posttranslational biosynthesis process. Through their GAG chains, HSPGs facilitate neural stem cell self-renewal, proliferation, lineage specification, differentiation and maintenance [10]. Work by our team and others have suggested HSPGs as biomarkers of human neural fate decisions to better identify, define, and isolate neural subpopulations [11,12].

As essential regulators of neurogenesis, growth factors are often used in an auxiliary strategy to improve properties of in vitro neural cultures [13]. The HS-binding proteins [14,15,16], brain-derived neurotrophic factor (BDNF) and platelet-derived growth factor (PDGF) are neuroregulatory growth factors often used in neural inductive cultures for specific lineage differentiation of various stem cell types [17,18,19,20,21,22]. BDNF is a neurotrophin with a diverse range of effects during brain development, including the promotion of neural cell proliferation, differentiation, maturation, survival and synaptic plasticity [23,24,25,26,27]. Interestingly, studies have demonstrated that BDNF may support serotonergic neuron differentiation in mice via the induction of S100 calcium-binding protein B (S100B) secretion from astrocytes [28]. Astrocytes have been shown to express higher levels of BDNF when compared to neuronal lineages [29], although overall BDNF expression remains relatively low in all human neural cells [30]. While the majority of the functions of BDNF are associated with promoting neurogenesis—often mediated through astrocytic secretions— PDGF has been implicated in not only neurogenesis and dendritic development but also in gliogenesis, highlighting its broader role in neural lineage specification [31,32,33]. The interactions between BDNF and PDGF with HSPGs are not well understood in the context of human neurogenesis, with investigations into their interactions likely to provide improved methods for the identification and differentiation of NPCs.

We have previously shown HSPGs as critical proteins in the maintenance and neural differentiation of embryonic stem cell (ESC)-derived human neural stem cells (hNSC H9 cells) [11,12], cortex-derived normal human neural progenitor cells (hnNPCs) [34], and human mesenchymal stem cell (hMSC) populations [35]. Specifically, GPC-1 and -4 were found to be novel markers of neuronal differentiation, as validated through targeted small interfering RNA (siRNA) knockdown (KD) of GPC1 and GPC4 in short-term (15 – 18 days) and long-term (40 – 60 days) neuronal differentiation of hNSC H9 cell populations [11,12]. GPC1 and GPC4 were also observed to be differentially expressed along neurites and cell bodies of long-term differentiating neurons, with a higher GPC4:GPC1 expression ratio observed in response to BDNF treatment, and lowered GPC4 expression in PDGF-treated cultures [12]. In addition, siRNA KD of GPC1 and GPC4 resulted in reduced neuronal marker expression and altered responsiveness to BDNF and PDGF [12], demonstrating the importance of these HSPGs in human neurogenesis.

This study aimed to identify human lineage-specific HSPG signatures that may serve as markers of glial cell differentiation, particularly in response to distinct neuroinductive conditions. The overarching goal was to establish a robust and reproducible method for generating functional astrocyte cultures in vitro, using commercially available human NPC lines. The use of cell lines provides the advantage of maintaining a stable phenotype across time in culture (passages) and overcomes the limited cell expansion capability associated with primary cell populations [36]. The human neural cell lines used included: the SH-SY5Y human neuroblastoma cell line, and the human induced NSC lines ReNcell VM (ventral mesencephalon-derived) and ReNcell CX (frontal cortex-derived). The SH-SY5Y human neuroblastoma cell line, commonly differentiated into mature neuronal cells, serves as a well-characterised, neuronally committed model resembling immature catecholaminergic neurons [37,38]. As such, it was included as a neuronal control to facilitate comparison of marker expression and HSPG profile changes. The two ReNcell lines are stable and commercially available models, shown to exhibit distinct electrophysiological properties following differentiation. This is likely due to differences in their derivation methods - ReNcell VM cells being derived from bulk foetal brain tissue, while ReNcell CX cells originate from a single cell clone [36,39,40]. The ReNcell CX cell line shares similar neural marker expression, neuronal and glial lineage potential, characteristic in vitro with hESC-derived hNSCs (39). Microarray analysis has shown ReNcell CX cells to differentially express ~12.4% of all genes compared to hESC-hNSCs, and to be more distant from hESCs when compared to hNSCs using principal component analysis [39], suggesting ReNcell CX cells possess fewer stemness and more NPC-like characteristics. Although both lines are capable of differentiating into mature neural lineages, the resulting cultures tend to be heterogeneous, with neural subtypes emerging stochastically upon withdrawal of growth factors such as fibroblast growth factor (FGF) and epidermal growth factor (EGF) [36].

In this study, the cell lines were first cultivated under their specific optimal basal conditions to prevent the introduction of any bias from changes in culture conditions. We aimed to establish a defined and reproducible astrocyte induction protocol for the heterogenous ReNcell VM NPC line, with differentiated SH-SY5Y cells serving as a neuronal comparator and ReNcell CX-derived astrocytes as a glial benchmark. By profiling key HSPG markers, we investigated how BDNF and PDGF influence lineage specification and glial commitment. These HSPG signatures may not only serve as markers of lineage progression but also provide actionable targets for steering NPC fate—either through selective molecular interventions or the design of small molecules modulating HS side-chain structures for tailored neural subtype generation.

2. Materials and Methods

2.1. Human Neural Cell Line Propagation and Neural Lineage Differentiation

2.1.1. SH-SY5Y Human Neuroblastoma Cell Line

The SH-SY5Y cell line (RRID:CVCL_0019) was routinely cultured as a monolayer in Basal Growth Medium (DMEM/F-12+GlutaMAX-I (Gibco, Cat #: 10565018) supplemented with 10% foetal bovine serum (FBS; Serana, Cat# S-FBS-AU-015) and 1% penicillin/streptomycin (pen/strep; Lonza, Cat# 17-602E)). The SH-SY5Y cells were differentiated toward the neuronal lineage using the protocol as described previously and from here on will be referred to as neuronal inductive cultures (41). Briefly, cells were plated onto 35 mm culture dishes at 1.0 x 10⁵ cells/dish in SH-SH5Y Basal Growth Media and allowed to attach overnight. Warmed and pH equilibrated (37°C, 5% CO2) SH-SY5Y Differentiation Media #1, comprised of DMEM/F-12+GlutaMAX-I supplemented with 2.5% heat-inactivated FBS (hiFBS), 1% pen/strep and 10 μM all-trans retinoic acid (ATRA; Sigma-Aldrich, Cat# R2625), was then added to replace the growth media, initiating Day 1 (D1) of differentiation. Media was changed using Differentiation Media #1 on D3 and D5. On D7, cells were replated onto fresh 35 mm dishes in Differentiation Media #1 and allowed to reattach overnight. Media was changed to warmed and equilibrated Differentiation Media #2 (DMEM/F- 12+GlutaMAX-I supplemented with 1% hiFBS, 1% pen/strep and 10 μM ATRA) on D8. On D10, cells were replated onto Geltrex^TM (Thermo Fisher Scientific, Cat# A1413202)-coated 24-well plates in Differentiation Media #2. Warm and equilibrated Differentiation Media #3 (Neurobasal media (Gibco^TM, Cat# 21103-049) supplemented with 1X B-27^TM Supplement (Gibco^TM, Cat# 17504044), 20 mM KCl, 1% pen/strep, 2 mM GlutaMAX-I^TM (Gibco^TM, Cat# 35050-061), 50 ng/mL BDNF (Invitrogen^TM, Cat# PHC7074), 2 mM db-cAMP (STEMCELL^TM Technologies, Cat# 73884) and 10 μM ATRA) was used to replace the media on D11, then two further media changes were performed on D14 and D17. Homogenous, mature neuronal cultures were ready for more detailed examination on D18.

2.1.2. ReNcell CX Human Neural Progenitor Cell Line

The ReNcell CX cell line (EMD Millipore, Cat# SCC007, RRID:CVCL_E922) was routinely expanded as a monolayer on laminin-coated (20 μg/mL; Invitrogen^TM, Cat# 23017-015) culture vessels in DMEM/F-12 + GlutaMAX-I supplemented with 20 ng/mL FGF-2 (Gibco^TM, Cat# PHG0024) and 20 ng/mL epidermal growth factor (EGF; Gibco^TM, Cat# PHG0314). Differentiation towards the astrocyte lineage was performed by first withdrawing growth factors (FGF-2, EGF) and allowing spontaneous differentiation (SD) for 3 days on Geltrex^TM-coated culture vessels. Differentiating ReNcell CX cells were then transferred to uncoated culture vessels (tissue culture plastic) in astrocyte differentiation media consisting of DMEM medium supplemented with 2% FBS, 2% N-2 Supplement (Gibco^TM, Cat# 17502048) and 2 mM GlutaMAX-I (media formulation from Thermo Fisher Scientific) for up to 2 weeks (14 days). Astrocyte differentiation media was changed every 3 – 4 days. ReNcell CX differentiation cultures from here on will be referred to as ReNcell CX astrocyte inductive cultures.

2.1.3. ReNcell VM Human Neural Progenitor Cell Line

The ReNcell VM cell line (EMD Millipore, Cat# SCC008, RRID:CVCL_E921) was maintained as a monolayer on laminin (20 μg/mL)-coated 10 cm² plates in ReNcell NSC Maintenance Medium (EMD Millipore, Cat# SCM005) supplemented with 20 ng/mL of FGF-2 and 20 ng/mL of EGF. For neural differentiation, ReNcell VM cultures underwent unguided/spontaneous differentiation on Geltrex-coated plates initiated by withdrawal of growth factor (FGF-2, EGF), which resulted in an untreated (UT) heterogeneous neural culture examined at D14. These cultures will be referred to as UT / spontaneous ReNcell VM neuroinductive cultures. Additionally, ReNcell VM neural differentiation cultures were supplemented with neuroregulatory growth factors, 10 ng/mL of BDNF and 10 ng/mL platelet-derived growth factor BB (PDGF-BB; Sigma-Aldrich^®, Cat# P4056-50UG) to direct lineage specification. The following culture conditions were examined: UT/spontaneous differentiation (spontaneous ReNcell VM neuroinductive cultures), +BDNF and +PDGF. Growth factors were re-applied to the cells every 3 – 4 days during media changes. The generated neural cultures were examined on D14.

2.2. Viability Assay

Cell viability of cell line-derived neural specific lineage cultures were assessed by fluorescein diacetate (FDA; live)/propidium iodide (PI; dead) staining. FDA (Sigma-Aldrich^®, Cat# F7378) and PI (Sigma-Aldrich^®, Cat# 81845) were added to unfixed neural cultures at 1:1000 dilution and incubated at room temperature for 10 min in the dark. Detection was performed on an Olympus IX81 phase-contrast fluorescent microscope using FITC (FDA/live) (Excitation = 490 nm, Emission = 530 nm) and Texas Red (PI/dead) (Excitation = 590 nm, Emission = 620 nm) filters. Live/Dead percentages were generated by using Volocity Cellular Imaging & Analysis Software v6.3 (Quorum Technologies Inc.) to count FDA-positive cells and PI-positive nuclei.

2.3. Fluo-4 Calcium Signalling Assay

Neuronal calcium signalling, indicative of the critical function of neurotransmission, was examined using the fluorescent calcium indicator, Fluo-4 Direct^TM (Invitrogen^TM, Cat# F10471), as described previously (12). Briefly, all cells tested for calcium signalling were plated at the appropriate seeding density in 96-well (0.32 cm²) plates. 2X Fluo-4 Direct^TM calcium reagent loading solution was prepared by adding Hanks' Balanced Salt Solution (HBSS) with 2 mM CaCl2 and 0.1 mM MgCl2 and 250 mM probenecid. Cells cultured on 96-well plates were incubated with equal volume to culture media of Fluo-4 (1X final concentration) for 45 min at 37°C then allowed to cool to room temperature (approx. 20 min) prior to imaging. Fluo-4 Direct^TM has an Em λ = 494 nm and Ex λ = 516 nm and was detected using the fluorescein isothiocyanate (FITC) filter on an Olympus IX81 microscope with a Hamamatsu Orca Camera using the Volocity Image Capture and Analysis Software v 6.3. Cultures were imaged for 200 sec at 0.8 sec intervals, equating to 251 captured time-points. At each time-point, fluorescence level of ten (10) regions of interest (ROIs) were measured using Volocity. Fluorescence signal intensity (FI) was normalised to time-point 1 (F0) and FI/F0 in Microsoft Excel and was graphed using the ‘stackedplot’ function in MATLAB (R2018b, RRID:SCR_001622).

2.4. Total RNA Isolation, cDNA Synthesis and Q-PCR

Gene expression analysis was carried out as previously described (42). Briefly, RNA isolation was carried out using Direct-zol™ RNA MiniPrep kit (Zymo Research Corp., Cat# R2052) with in-column DNase I (300 U/rxn) treatment. RNA conversion to cDNA was performed using the iScript cDNA Synthesis Kit (Bio-Rad, Cat# 170-8891) following the manufacturer’s instructions. Briefly, 150 ng of RNA template was reverse transcribed using 4 μL of 5X iScript Reaction Mix, 1 μL of iScript Reverse Transcriptase, and nuclease-free water to a total reaction volume of 20 μL. Samples were incubated for 5 min at 25°C (priming), 20 min at 46°C (reverse transcription), 1 min at 95°C (Reverse Transcriptase inactivation), and then held at 4°C.

Human neural cultures generated in this study were characterised for gene expression of HSPG core protein, GAG biosynthesis machinery, as well as pluripotency and neural specific lineage markers. Q-PCR was performed in 384-well plates using the Applied Biosystems® QuantStudio-7 Flex Real-Time PCR System (Life Technologies) where three biological replicates per culture condition was assayed in technical quadruplicate. For each reaction, 120 ng of cDNA was amplified with 5μL of 1X SYBR Green Mix (Promega, Cat# A6002), 200 nM of each primer pair and 0.1 μL ROX Passive Reference Dye (Promega) in a final reaction volume of 10 μL. The cycling conditions were as followed: 50°C × 2 minutes, 95°C × 3 minutes followed by 50 cycles at 95°C × 3 seconds, 60°C × 30 seconds. Gene expression was normalised against expression of rRNA 18S, an endogenous control gene. All primers used in this study have been validated in several previous studies from the research group (11, 12, 35, 42-44).

Gene expression data from neural cultures were combined between experimental replicates and analysed using the 2^-ΔCt method. Fold changes of target gene expression were calculated between basal and differentiated cultures. Growth factor modulated cultures were analysed as fold change compared to untreated (UT) differentiated cultures. Data is presented as Log2FoldChange vs. -Log(p-value) on volcano plots. Student’s T-test was used to determine significant changes in target gene expression levels between basal and differentiated cultures, and between culture conditions. Significance was set at α=0.05. Volcano plots were drawn using GraphPad Prism 9 software (Version 9.1.0, RRID:SCR_002798).

2.5. Immunocytochemistry (ICC) Analysis

To fix cells for immunostaining, cells on coverslips (13 mm, plastic) in 24-well plates (Sarstedt) were first partially fixed by gently removing 70% of the media, which was then replaced with 4% paraformaldehyde (PFA) for 2 min, followed by a complete fix with fresh 4% PFA for 20 min at room temperature (RT). Cells were permeabilised and antigen blocking performed by incubation with 2% normal donkey serum (NDS) + 0.3% Triton-X in PBS with Ca²⁺ and Mg²⁺ for 3 hr at RT with gentle rotation. Primary antibodies diluted in 2% NDS in PBS were added to the cells and incubated, static, overnight at 4°C. The primary antibodies and dilutions used were: anti-SOX2 (1:1000; Millipore, Cat# AB5603, RRID:AB_2286686), anti-MAP2 (1:200; Abcam Cat# ab36447, RRID:AB_776175), anti-GFAP (1:250; Abcam, Cat# ab7260, RRID:AB_305808), anti-O1 (1:500; Millipore, Cat# MAB344, RRID:AB_94860), and anti-HS 10E4 (1:1000; Amsbio, Cat# 370255-1, RRID:AB_10891554). The next day, primary antibodies were removed, cells washed 3 x 10 min with washing solution (0.2% NDS + 0.03% Triton-X in PBS) and secondary antibodies diluted in 2% NDS in PBS were then applied to the cells for 2 hr at RT. Following 3 x 10 min washes with washing solution (0.2% NDS + 0.03% Triton-X in PBS), cells on coverslips were placed on glass microscope slides with cells facing up and mounted using ProLong^TM Gold AntiFade Mountant with 4',6-diamidino-2-phenylindole (DAPI) counterstain (Life Technologies, Cat# P36941) with another coverslip placed on top of the cells. Slides were imaged using an Olympus IX81 inverted phase-contrast fluorescence microscope with a Hamamatsu Orca R2 Camera using the Volocity v6.3 Image Capture and Analysis Software (Quorum Technologies Inc., RRID:SCR_002668) at 20X magnifications. Image contrast, brightness and sharpness of images acquired were processed using Fiji (ImageJ2 v2.1.0/1.53c, RRID:SCR_002285) software. Quantitation of the percentage of signal positive cells was performed by manual cell counting, where three individual images from each experimental replicate (n=3) were used for quantitation. The results are presented as mean with standard deviation (SD) with statistical testing performed using unpaired t tests with Welch’s correction. For differentiated ReNcell VM neural cultures, due to the abundance of neuronal protrusion and cell numbers, ICC images were quantitated using signal intensity normalised to cell numbers.

2.6. Western Blotting

Western blot (WB) analysis was used to detect HSPG core proteins during ReNcell VM differentiation with PDNF and PDGF, utilising the 3G10 neo-epitope. For all other experiments, specific SDC3 and GPC2 antibodies were applied for protein detection. The 3G10 neo-epitope is only generated following digestion of HS GAGs by heparitinase, where the 3G10 antibody reacts with desaturated hexuronate “stubs” that remain on the core proteins (45). Thus, HSPG core protein forms can be visualised by 3G10 staining, detected as multiple bands on WBs. The sizes of the HSPG cell surface core proteins are as follows (from GeneCards® The Human Gene Database): syndecan-1 (SDC1; 32 kDa), syndecan-2 (SDC2; 22 kDa), syndecan-3 (SDC3; 45 kDa), syndecan-4 (SDC4; 22 kDa), glypican-1 (GPC1; 62 kDa), glypican-2 (GPC2; 63 kDa), glypican-3 (GPC3; 66 kDa), glypican-4 (GPC4; 62 kDa), glypican-5 (GPC5; 64 kDa), glypican-6 (GPC6; 63 kDa). WB analysis of human neural cell line basal and neural inductive cultures was conducted as previously described (12, 34-42, 46). Briefly, technical triplicates of cells grown in basal and neural inductive culture conditions of each cell line were pooled prior to protein collection and total protein extracted using RUNX protein-lysis buffer with protease and phosphatase inhibitor (1:100; Cell Signaling Technology^®, Cat# 5872). Protein samples were quantitated using the Qubit Protein Assay Kit (Thermo Fisher Scientific, Cat# Q33211) and a Qubit 2.0 Fluorometer (Thermo Fisher Scientific). Approximately 20–30 μg of protein was separated by SDS-PAGE using 12% TGX^TM FastCast^TM Acrylamide gels (Bio-Rad, Cat# 1610175) and transferred onto 0.2 μm PVDF membranes (EMD Millipore Corp., Cat# ISEQ00010) using the Transblot turbo system (Bio-Rad). The membrane was blocked with 5% skim milk in TBST (Tris-buffered saline + 0.1% Tween-20) followed by addition of primary antibodies diluted in 5% bovine serum albumin (BSA) in TBST and incubated overnight at 4 °C. The primary antibodies used include: anti-Δ3G10 (1:1000; US Biological, Cat# H1890-75, RRID:AB_2722745), anti-GPC2 (1:2000, Invitrogen, Cat#PA5-115299, RRID:AB_2899935), anti-SDC3 (1:1000; abcam, Cat# ab63932, RRID:AB_1143216) with GAPDH (1:1000; Cell Signaling, Cat# 2118, RRID:AB_561053) used as the loading control. Primary antibodies were removed the next day, membranes washed in TBST followed by incubation with HRP/fluorophore-conjugated secondary antibodies (1:3000; anti-Mouse IgG, Cell Signaling, Cat# 7076, RRID:AB_330924; anti-Rabbit IgG, Cell Signaling, Cat# 7074, RRID:AB_2099233; 1:10000; Alexa Fluorophore 488 anti-Mouse IgG, Thermo Fisher Scientific, Cat#A10680, RRID:AB_2534062 and 1:10000; Cyanin 3 anti-Rabbit IgG, Thermo Fisher Scientific, Cat#A10520, RRID:AB_10563288) for 2h at room temperature. Target protein detection was performed with enhanced chemiluminescence (Clarity ECL, Bio-Rad, Cat# 1705060) using the Fusion FX Spectra chemiluminescence system (Vilber Lourmat, Fisher Biotec) and each blot quantitated using Image J software (version 1.52q, NIH, RRID:SCR_003070).

3. Results

3.1. Human Neural Cell Line Cultures Adapt Neural Cell Morphology, Maintain High Cell Viability, and Exhibit Spontaneous Calcium Activity Following Neuroinductive Cultures

The three neural cell lines studied, SH-SY5Y, ReNcell CX and ReNcell VM, were grown as monolayers under basal expansion conditions as described above. Basal SH-SY5Y cells grew in clusters with non-polarised cell bodies and few condensed processes (Figure 1a). During SH-SY5Y neuronal induction, cell bodies became pyramidal with neurite-like extensions. Adherent spheres were observed at the endpoint of this study (D18) with inter-spherical connections observed (Figure 1b). ReNcell CX cells were polygonal in morphology during basal culture with several protrusions observed, at high density these cells a cobble-stone pattern (Figure 1d). When examined following astrocyte inductive culture, astrocyte-like processes were observed within the cultures, with cells displaying a “star-like” morphology by day 14 (D14) of differentiation (Figure 1e). There was a lack of secondary and tertiary structures such as branches and peripheral fine processes observed in these cultures, characteristics of mature astrocytes (47). Undifferentiated ReNcell VM cells changed from a “paving stone” morphology at the start of the neuroinductive culture period (Figure 1g) to a classic neuron-like morphology with small cell bodies and visibly elongated dendritic-like processes after D14 of neuroinductive culture (Figure 1h). All three human neural cell lines maintained high viability as analysed by FDA/PI staining, with SH-SY5Y neuronal cultures maintaining an average of 98% viability, the ReNcell CX astrocyte inductive cultures maintaining an average of 97% viability and the ReNcell VM spontaneous neuroinductive cultures maintaining an average of 94% viability (Figure 1c, 1f, 1i, and 1j).

Fluo-4 calcium indicator dye was added to cell line-derived neural lineage inductive cultures to detect any spontaneous calcium oscillation, a characteristic of neural cell cultures and an indirect method of examining spontaneous action potentials representative of functionality (48). Calcium signalling activity in cell line-derived neural specific cultures was compared to the hNSC H9 neuronal cultures at D60, with known oscillatory activity [30]. In the positive control cultures, hNSC H9 D60 neuronal cells exhibited a “wave-like” pattern of calcium signals over time, indicative of spontaneous calcium oscillation (Figure S1a, Online Resource 1). In a non-neural cell type, such as the human breast cancer (HBC) cell line MCF-7, slow uptake of Fluo-4 was observed, indicating a lack of cell-cell communication via calcium signalling (Figure S1b, Online Resource 2). The cell line-derived neural lineage specific cultures, SH-SY5Y neuronal inducted cultures at D18 displayed a similar wave pattern of calcium signal to the hNSC H9 Neuronal D60 cultures (Figure 1k, Online Resource 3), indicating spontaneous calcium oscillations. Calcium signals from ReNcell CX astrocyte inductive D14 cultures were observed to be similar to those reported for astrocyte cultures, described as global waves, local waves and microdomains (49), which together appear as calcium bursts and intrinsic fluctuations (50), (Figure 1l ROIs 5 and 7 ; Online Resource 4). Interestingly, in the ReNcell VM spontaneous neuroinductive cultures, slow uptake of Fluo-4 was observed, similar to the uptake observed in MCF-7 HBC negative control cultures, suggesting lack of neural functionality, likely due to a mixture of non-committed NPC populations within the cultures (Figure 1m, Online Resource 5).

3.2. SH-SY5Y Neuronal Differentiated Cultures Exhibit Similar Characteristics to Differentiated hNSC H9 Cells

The SH-SY5Y neuronal inductive cultures were then further characterised for neural lineage marker expression and changes in HSPG profile. ICC analysis of SOX2, a key transcription factor in NSC maintenance (51), was shown to be widely expressed by basal SH-SY5Y cells (Figure 2a), and to be reduced and lowly expressed in the neuronal inductive cultures (Figure 2b). SOX2 localisation can be nuclear and/or cytoplasmic depending on cell type, self-renewal (stem cell) or lineage (differentiation) state (52). Cytoplasmic localisation of SOX2 was observed in SH-SY5Y cells, likely due to the acetylation of SOX2, previously reported in ESC differentiation (53) and observed in a human mesencephalic cell line (54). The cytoplasmic SOX2 expression observed in the basal SH-SY5Y cultures are reminiscent of NPCs. Quantitation of SOX2 expression showed a significant decrease (p=1.28e-05) in the number of SOX2+ cells following SH-SY5Y neuronal induction (86±24% reduced to 2±5%) of SOX2+ cells (Figure 2c). Expression of MAP2, the mature neuronal marker, was observed to be significantly increased (p=1.69e-05) within the SH-SY5Y neuronal cultures, with 0.8±0.9% MAP2+ cells to 80±12% MAP2+ cells detected by D21 (Figure 2d-f). Interestingly, SH-SY5Y basal cultures expressed high levels of glial lineage markers, which were observed to be maintained throughout neuronal inductive culture (Figure 2g-h). The expression of the astrocyte marker GFAP was found to be maintained at 94±9% and 98±3% GFAP+ cells in basal and inductive cultures, respectively (Figure 2i). O1 is considered a marker of late oligodendrocyte progenitors (55), with undifferentiated SH-SY5Y cells stained strongly for this marker (Figure 2j; 87±22% O1+ cells), with staining found to be maintained at a lower level (58±24% O1+ cells) in the inductive cultures (Figure 2k-l).

Gene expression analysis showed a significant downregulation of several stem cell and neural lineage markers, including the pluripotency markers (POU5F1; p=0.0016, and NANOG; p=8.06e-05), NPC markers (SOX1; p=0.0011, SOX2; p=2.69e-05, and NES; p=0.0154), astrocyte markers (S100B; p=0.030, SLC1A3; p=0.0115), and oligodendrocyte marker (GALC; p=0.0457) (Figure 2m). Interestingly, the gene expression level of the neuronal markers, NEFM (p=0.0003) and MAP2 (p=0.0027), was found to be significantly downregulated (Figure 2m). In contrast, the neuronal marker TUBB3 (p=0.0297) was observed to be significantly upregulated, along with the oligodendrocyte marker OLIG2 (p= 0.0475; Figure 2m). Overall, the SH-SY5Y neuronal inductive cultures displayed a neuronal phenotype, evident from the cellular morphology, calcium activity along with the gene/protein expression of neuronal markers.

3.3. Glypican 2 Predominate in Neuronal Differentiated Cultures

Amongst the HS GAG biosynthesis and modification enzymes, HS chain elongation enzyme EXT2 (p=0.0059) as well as the 6-O-endo-sulfatase SULF2 (p=8.32e-09) were found to be significantly upregulated in neuronal inductive SH-SY5Y cultures, indicating an increased length of HS GAGs and/or the number of HS chains within these cultures, as well as modifications at the 6-O-sulfation sites. Furthermore, gene expression levels of several N-deacetylase and N-sulfotransferases, NDST1 (p=3.39e-06), NDST2 (p=5.78e-05), and NDST4 (p=0.0036) were observed to be significantly downregulated, along with the HS 6-O-sulfotransferase, HS6ST1 (p=0.0006) (Figure 2n) in neuronal inductive SH-SY5Y cultures. This data suggested a decrease in sulfation requirement at the N- and 6-O-sulfation sites following SH-SY5Y neuronal induction with medication of of N- and 6-O-sulfation sites reported during stem cell neural differentiation (56). ICC analysis of HS GAG content of SH-SY5Y cultures was performed using the pan-HS 10E4 antibody. The 10E4 epitope contains N-sulfated glucosamine residue/s which react with the antibody allowing detection of all HS GAG chains (57, 58). In basal SH-SY5Y cells, 10E4 was demonstrated to have punctuated expression and as cells differentiated towards the neuronal lineage, 10E4 expression became more widespread and localised to the cell surface (Figure 2s). Quantitation of 10E4 signal intensity showed a >2-fold increase (p=0.0098) in the intensity of 10E4 staining in neuronal inductive cultures when compared to basal SH-SY5Y cultures (Figure 2r) demonstrating acquisition of neuronal phenotypes coinciding with increased GPC expression and HS GAG content.

There was a significant upregulation of GPC2 (p=0.04996) gene expression, along with the significant downregulation of SDC1 (p=0.0149) (Figure 2n) in the neuronal inductive SH-SY5Y cultures. WB analysis of polyclonal GPC2 and SDC3 in SH-SY5Y-derived neuronal cultures revealed an interesting core membrane-bound HSPG protein profile post-lineage induction. In basal SH-SY5Y cells, all members of the SDC3 family, including membrane-bound SDC3 (MB SDC3, 45kDa), truncated membrane-bound SDC3 (TMB SDC3, 19kDa) (59), and cytoplasmic domain SDC3 (CD SDC3, 12 kDa) (60), were found to be expressed. However, in the inductive neuronal SH-SY5Y cultures, glycosylated or neural GPC2 (100kDa) was observed to be the predominant form, along with membrane-bound GPC2 (MB GPC2, 63kDa) (Figure 2o). Quantification of WB signals indicated reduced expression of all SDC3 family members (MB, TMB, CD) in the neuronal cultures (Figure 2p), correlating with the observed significant decrease in SDC3 gene expression. Notably, SDC3 exhibited the lowest relative gene expression levels in neuronal cultures when compared to basal cultures (Figure 2n). Interestingly, while MB GPC2 expression was found to be lower in the neuronal inductive cultures, neural GPC2 was also found to be highly expressed in these cultures, but undetected in SH-SY5Y basal cultures. As a result, total GPC2 expression in neuronal cultures exceeded that of the basal cultures (Figure 2q), aligning with the observed significant upregulation of GPC2 gene expression (Figure S2a).

3.4. ReNcell CX Astrocyte Induction Conditions Produce an Immature Astrocyte Culture in 14 Days

ICC analysis showed the NSC marker SOX2 to be widely expressed by ReNcell CX basal cells (Figure 3a), comparable to SH-SY5Y basal cultures, and lower in ReNcell CX astrocyte inductive cultures (Figure 3b). Quantitation of this data identified 85±9% SOX2+ cells in basal cultures, with a significant reduction (p=0.0012; 49±16%) of SOX2+ cells in the astrocyte inductive cultures (Figure 3c). The neuronal marker MAP2 was not found to be expressed in basal ReNcell CX cultures, although a subpopulation (31%±20%, p=0.0268) of MAP2+ cells were identified in the ReNcell CX astrocyte inductive culture conditions (Figure 3d-e). In addition, a significant increase in the expression of the astrocyte marker GFAP (p=0.0043) was observed as ReNcell CX astrocyte inductive cultures (from 73±16% to 96±4% GFAP+ cells; Figure 3g-i). Examination of the oligodendrocyte marker O1, revealed the basal ReNcell CX cultures contained 20±19% O1+ cells, with 32±15% O1+ cells observed in the astrocyte inductive culture of these cells (Figure 3j-l).

When compared to basal cultures, ReNcell CX astrocyte inductive cultures were found to express a significantly lower level of pluripotency and NSC gene markers, POUF51 (p=0.0195), SOX2 (p=0.0456), and NES (p=0.0054), correlating with decrease SOX2+ cells (Figure 3m). The neuronal marker NEFM (p=0.0144) was also found to be significantly downregulated (Figure 3m), confirming a global reduction in neuronal lineage potential within the astrocyte inductive culture conditions. During human brain development, the astrocyte gene SLC1A3, which encodes for excitatory amino acid transporter 1 (EAAT1), is primarily expressed by developing astrocytes with SLC1A2 (EAAT2) expressed by adult astrocytes (61). In ReNcell CX astrocyte inductive cultures, SLC1A3 (p=0.0018) was found to be significantly downregulated, with the mature astrocyte marker SLC1A2, expressed at a similar level to basal cultures (Figure 3m). This suggested cells within these inductive cultures have committed to the astrocyte lineage, yet remain immature, with longer time in culture likely needed to produce a more mature, homogenous population of astrocytes. Indeed, several existing astrocyte differentiation protocols require at least 30 days or up to 4 weeks in culture to generate mature astrocytes (62-65).

3.5. Increase in HS Production Is Characteristic of Astrocytic Lineage

Significant downregulation of NDST2 (p=0.0143), NDST4 (p=0.0411), and HS2ST1 (p=0.0387) (Figure 3n), suggested a decrease or minimal change in both N- and 6-O-sulfation patterns following astrocyte lineage induction in the ReNcell CX cells. The HS elongation enzymes, EXT1 (p=0.0248) and EXT2 (p=0.0018), and the epimerisation enzyme, C5-EP (p=0.0007), were found to be significantly upregulated in the astrocyte inductive cultures (Figure 3n), indicating increased GAG formation. Basal ReNcell CX cultures stained with 10E4 antibody showed HS GAGs to be diffusely distributed across the cell surface, and as cells committed the astrocyte lineage, these HS GAGs formed localised dense clusters along the cell surface (Figure 3r). This was supported by quantitation of 10E4 signal intensity demonstrating astrocyte inductive cultures to have significantly higher (p=0.0018; 2.7-fold) HS GAG content when compared to basal ReNcell CX cultures (Figure 3s).Following astrocyte lineage induction, ReNcell CX cultures differentially expressed several HSPG core proteins, including the significant downregulation of SDC1 (p=0.0013), SDC2 (p=0.0013), and GPC1 (p=0.0005), and the significant upregulation of SDC4 (p=0.0018) and GPC6 (p=0.0417) gene expression (Figure 3n).

WB analysis revealed distinct subtype-specific expression patterns for both GPC2 and SDC3 proteins in ReNcell CX cultures under basal and astrocyte inductive conditions. GPC2, neural-specific isoform expression, commonly enriched in neuronal precursors, was absent in basal cultures but became weakly detectable under astrocyte inductive conditions, indicating a modest upregulation upon lineage specification. Interestingly, the MB isoform of GPC2 was found to be weakly expressed in both basal and astrocyte-induced cultures, although the signal remained faint and below levels typically observed in highly neurogenic environments. These observations suggest that while astrocyte-inductive cues may transiently activate GPC2 expression, particularly of the neural isoform, this activation is relatively subdued, possibly reflecting an intermediate or transitional state rather than full neurogenic commitment. The low-level MB GPC2 expression in both conditions may reflect a basal role for GPC2 in maintaining minimal membrane signalling functions in progenitor cells, independent of lineage trajectory. This is supported by prior studies showing GPC2 interaction with Wnt and Hedgehog signalling components via its HS side chains, with its function tightly downregulated as progenitors transition to a glial lineage (66, 67). Moreover, the low neural GPC2 signal in the astrocyte-inductive cultures may reflect residual heterogeneity or limited co-expression of early neuronal markers during the initial phases of glial lineage priming. In contrast, SDC3 exhibited a divergent regulatory profile. While transcript levels remained largely unchanged between conditions, WB analysis showed that both the MB and CD isoforms of SDC3 were undetectable in astrocyte inductive cultures. This suppression was specific to astrocyte-directed differentiation, as basal conditions retained clear protein expression of both isoforms. The loss of detectable SDC3 protein in the astrocyte cultures underscores its post-transcriptional regulation and aligns with its known role in neural progenitor maintenance, axonal pathfinding, and response to growth factors such as FGF2 and EGF (68, 69). The coordinated downregulation of both MB and CD SDC3 also suggests a tightly controlled shut-off mechanism during glial commitment, potentially to enable the shift from progenitor plasticity to glial maturation. Together, these findings highlight the selective and isoform-specific modulation of GPC2 and SDC3 during astrocyte specification. While GPC2 showed a modest and possibly transitional upregulation of its neural isoform, SDC3 was robustly suppressed at the protein level, reflecting distinct regulatory dynamics underpinning neuroglial lineage segregation in human neural progenitor models.

3.6. ReNcell VM Mixed Neural Cultures Favour Neuronal Lineage, but Maintain NPC Subpopulation

Analysis of NSC (SOX2), neuronal (MAP2), astrocyte (GFAP) and oligodendrocyte (O1) markers by ICC indicated reduced NSC phenotype in the ReNcell VM spontaneous neuroinductive cultures, accompanied by increased neural-specific lineage markers. A significant decrease (p=8.73e-07) in SOX2+ cells was observed between basal (99±1%) and spontaneous neuroinductive (35±12%) ReNcell VM cultures (Figure 4a-c), indicating approximately two-thirds of the cells were lineage committed or differentiated, while a subpopulation remained as NPCs. Basal ReNcell VM cells do not express MAP2, however, following spontaneous neuroinduction, a small subset of MAP2+ cells (0.5%) was detected (Figure 4d-f), while GFAP and O1 signal intensity remained similar between the basal and spontaneous neuroinductive ReNcell VM cultures (Figure 4g-l).

Significant downregulation of NSC genes, MSI1 (p=0.0003) and ENO2 (p=1.83e-08), further supported the reduction of NSC phenotype in the spontaneous neuroinductive cultures. However, SOX2 (p=0.0018) gene expression, along with the other NSC markers SOX1 (p=0.0251) and NES (p=0.0109), was observed to be significantly upregulated (Figure 4m). Corresponding with ICC data, neuronal marker MAP2 (p=0.0008), along with NEFM (p=0.0427) and DCX (p=0.0367) were found to be significantly upregulated at the gene expression level. While ICC analysis indicated astrocyte and oligodendrocyte lineage markers maintained similar expression profiles in both basal and neuroinductive ReNcell VM cultures, astrocyte markers (GFAP; p=0.0048, S100B; p=0.0012, and SLC6A4; p=0.0292) along with oligodendrocyte markers (OLIG1; p=0.0288, and OLIG2; p=0.0317) demonstrated significantly increased gene expression levels (Figure 4m). These observations suggest a heterogeneous mixture of different neural cell populations within the spontaneous ReNcell VM neuroinductive cultures. This is similar to findings reported by other groups, where spontaneously differentiated ReNcell VM cultures were demonstrated to be comprised of cells at varying stages of maturation and to expresses lineage fate markers of both neuronal and glial lineages (36, 70).

3.7. Upregulation of Syndecan-1 Is Unique to ReNcell VM Mixed Neural Cultures

In Heterogeneous 10E4 staining was observed in basal ReNcell VM cultures, localised to specific areas within the culture (Figure 4r). Following spontaneous neuroinductive culture, 10E4 staining showed a homogenous pattern throughout the culture, with expression detected on the cell surface and in cell clusters, with no increase in overall 10E4 signal intensity (Figure 4r-s) observed, suggesting the distribution and localisation changed, but not the overall level of HS-GAGs within the cultures. Differences in localisation of HS GAGs between basal and inductive ReNcell VM neural cultures, in conjunction with the upregulation of HS enzymes, indicate active HS biosynthetic machinery throughout neural specification and remodelling of the HS profile during lineage induction and differentiation.

Interestingly, widespread significant upregulation of HSPG-related genes was observed in spontaneous neuroinductive cultures when compared to basal ReNcell VM cultures. All surface-bound HSPG core proteins (SDC1; p=0.0237, SDC2; p=0.0025, SDC3; p=0.0081, SDC4; p=0.0299, GPC1; p=0.0182, GPC2; p=0.0283, GPC3; p=0.0324, GPC4; p=0.0005, GPC5; p=0.0005, and GPC6; p=0.0016) were found to be significantly upregulated following spontaneous neuroinduction, along with majority of the HS biosynthesis and modification enzymes, except for EXT2, SULF2 and HPSE (Figure 4n). WB analysis to assess changes in GPC2 and SDC3 expression following ReNcell VM neuroinduction identified neural GPC2 and CD SDC3 expressed at very low levels in basal ReNcell VM cultures. In contrast, MB GPC2 and all other SDC3 isoforms, including MB and TMB SDC3, exhibited higher expression levels in basal when compared to spontaneously neuroinducted ReNcell VM cultures (Figure 4o–q). Upregulation of neural GPC2 and CD SDC3 was observed in these mixed neural cultures, resembling the expression patterns observed in the SH-SY5Y neuronal and ReNcell CX astrocyte inductive cultures. Notably, neural GPC2 expression was observed to be highest in SH-SY5Y neuronal cultures, followed by the spontaneous neuroinductive ReNcell VM, and lowest in ReNcell CX astrocyte cultures. These findings suggest that the highly glycosylated neural GPC2 correlated with increased neuronal marker expression.

3.8. HS-Binding Growth Factor BDNF Increased Neural Cell Numbers and PDGF Increased Oligodendrocyte Specficity

The ReNcell VM cells were then subjected to guided lineage specification in the inductive cultures via the supplementation of the HS-binding growth factors BDNF and PDGF-BB at 10 ng/mL. As previously described, our group has conducted extensive work with hNSCs, developing differentiation protocols via BDNF and PDGF-BB supplementation at 10 ng/mL (12). Culture viability analysis by FDA/PI showed growth factor-supplemented cultures maintained high viability, BDNF-treated cultures (89%) and PDGF-treated cultures (95%; Figure 5a-b). Cell numbers at D14 of ReNcell VM neural cultures with growth factor supplementation demonstrated that BDNF-treated cultures contained the highest averaged cell numbers, approximately 3-fold higher than untreated cultures (Figure 5c).

Fluo-4 calcium signalling analysis of ReNcell VM neural cultures supplemented with BDNF and PDGF exhibited minor calcium oscillations when examined at the D14 time-point (Figure 5d). Heterogeneity of calcium signal was observed for both BDNF (Online Resource 6) and PDGF-treated cultures (Online Resource 7). Several localised ROIs exhibiting “wave-like” calcium peaks were observed (ROIs 1 and 8 in BDNF-treated cultures, ROIs 7 and 9 in PDGF-treated cultures; Figure 5d), with the majority of cells within these cultures observed to only take up the Fluo-4 dye. However, in PDGF- treated cultures, higher calcium peaks (i.e., Figure 5d, ROI 7) were observed.

The neural phenotype of neuroinductive ReNcell VM cultures supplemented with BDNF and PDGF were further characterised by ICC and gene expression analyses. The percentage of SOX2+ cells in the BDNF and PDGF-supplemented cultures (30 – 40%) were not observed to be significantly different from UT or spontaneous ReNcell VM neuroinductive cultures (Figure 5e-f), suggesting growth factor modulation did not alter the proportion of progenitor cells. The neuronal marker MAP2 was found to be expressed in a minor percentage of cells in the ReNcell VM UT cultures, which significantly increased by ~2-fold (p=0.0277) in BDNF-supplemented cultures, resulting in approximately 1% of MAP2+ cells (Figure 5g-h). MAP2 is primarily responsible for stabilising microtubules in neurons (71), suggesting BDNF supplementation increased neuronal lineage capacity. The percentage of MAP2+ cells in the PDGF-supplemented cultures did not differ from the UT cultures. Examination of changes in glial lineage potential showed signal intensity of the astrocyte marker GFAP did not alter significantly following growth factor supplementation (Figure 5i-j), with the oligodendrocyte marker O1 signal intensity maintained in BDNF-treated and increased significantly in the PDGF-treated (p=0.0225) when compared to UT cultures (Figure 5k-l).

Examination of the changes in gene expression of neural lineage markers in ReNcell VM BDNF-supplemented neural inductive cultures identified the astrocyte marker SLC1A3 (p=0.0048) as the only marker to be significantly downregulated (Figure 6a). This observation suggests while the proportion of astrocytic cells may have increased, along with increased GFAP expression, the resulting astrocytes were immature in function. In the PDGF-supplemented ReNcell VM neural cultures, significant downregulation of the astrocyte markers S100B (p=0.0071), SLC1A3 (p=0.0161), and GFAP (p=0.0366) was observed (Figure 6c), suggesting suppression of the astrocyte lineage. Interestingly, exogenous PDGF has previously been shown to promote glial differentiation of human stem cells in vitro (72-74), thus it is likely that addition of PDGF to the ReNcell VM neural cultures in this study favoured promotion of oligodendrocyte over astrocyte lineage differentiation.

3.9. Growth Factor Supplementation to Neural Cultures Remodelled HS 6-O-Sulfation Sites

Both BDNF and PDGF-BB are HS-binding neuroregulatory growth factors, however, the effect of their exogenous supplementation on the HSPG profile of human NPCs has not been well characterised. Gene expression analysis of HSPG core proteins and biosynthetic enzyme genes in ReNcell VM neural cultures modulated with BDNF showed significant downregulation of GPC6 (p=0.0286) and significant upregulation of GPC5 (p=0.0157) when compared with ReNcell VM UT cultures (Figure 6b). The HS modification enzymes, HS6ST1 (p=0.0004) and SULF2 (p=0.0367), were also found to be significantly upregulated. The HS6ST1 enzyme facilitates 6-O-sulfation of HS (75), with SULF2 an endosulfatase which removes 6-O-sulfation (76). The upregulation of these two genes suggests ongoing modification at the 6-O-sulfate sites in response to exogenous BDNF. In the PDGF-modulated cultures, no significant changes in core protein gene expression were observed, however, significant upregulation of the enzyme genes HS6ST1 (p=6.19e-07) and HPSE (p=0.0378) (Figure 6d) was observed. HPSE is an endoglycosidase active during ECM remodelling by cleaving HS (77). Together with HS6ST1, these changes in gene expression suggest exogenous PDGF-BB resulted in localised ECM remodelling. WB analysis of HSPGs showed reduced expression of GPCs, SDC3 and SDC1 core proteins in the growth factor modulated ReNcell VM (Figure 6e), and ReNcell VM UT cultures (Figure 6f). Analysis of HS content in BDNF and PDGF-supplemented cultures showed similar 10E4 signal intensity to the UT cultures (Figure 6g-h).

4. Discussion

The cell surface bound SDC and GPC HSPGs are comprised of a core protein with at least one or more HS GAG chain attached. HS GAGs are the result of a complex post-translational biosynthethic processes involving a suite of enzymes (78). HSPGs are highly abundant in the NSC niche with a vast array of functions, including modulating NSC self-renewal, differentiation, lineage commitment and specification (10). However, many of the functions of HSPGs in human models of neurogenesis are still largely unknown. In this study, three human neural cell lines were explored and characterised to identify changes specific to astrocytic lineage capacity. We examined these neural cell lines under both basal expansion and inductive culture conditions to assess neural-specific marker expression alongside HSPG profiles, with the goal of developing a simple and reproducible astrocyte model from the commercially available progenitor lines. While neural cell lines are indispensable tools for advancing our understanding of human neurogenesis and cellular differentiation, they lack direct therapeutic applicability (79). Their value lies in their lineage differentiation potential, including into astrocytes, making them ideal for studying disruptions in lineage specification that may underlie dysfunctional or reactive astrocyte states implicated in neurodegenerative diseases (80). These cell lines offer an accessible, scalable platform for dissecting the molecular decision-making processes that govern astrocytic fate – an insight that ultimately translatable to primary cell and therapeutic models. Given their reproducibility and ease of use, the cell models used in this study provide a powerful framework to construct an HSPG-based molecular roadmap for astrocyte induction and glial lineage commitment.

We showed that at D14, ReNcell CX cells exhibited spontaneous calcium oscillatory activity consistent with astrocytic signalling patterns, whereas differentiated SH-SY5Y cells displayed activity more indicative of neuronal lineages. In contrast, ReNcell VM cultures only exhibited comparable oscillatory patterns under growth factor-supplemented conditions, with PDGF treatment eliciting notably higher Ca²⁺ peak amplitudes. This data underscored the intrinsic heterogeneity of the ReNcell VM population and highlighted the limitations of short-term differentiation protocols in achieving lineage-specific homogeneity. The enhanced oscillatory response to PDGF may reflect an enrichment of glial-biased progenitors within the VM population, with PDGF potentially driving differentiation toward oligodendrocyte-like states.

Previous studies conducted by our group examined hNSC H9 neuronal differentiation in short term (D15 – 18) and long-term cultures (D40 – 60) (12, 46). Similar to SH-SY5Y neuronal cultures, the D15-18 hNSC cultures also expressed the immature neuronal markers TUBB3, NEFM and DCX with downregulation of the astrocyte marker S100B (11). Differences in cell morphology were also observed, with SH-SY5Y neuronal cultures displaying cell clustering, not characteristic in hNSC H9 neuronal cultures. The SH-SY5Y and hNSC H9 neuronal cultures were examined under different inductive culture conditions, likely influencing differences in stage of maturation between the two cell types, despite being in lineage differentiation inductive culture conditions for a similar length of time. Neuronal D60 hNSC H9 cultures also showed significant gene expression of the mature neuronal marker MAP2, as well as small cell bodies with long dendritic-like processes, and the formation of neural clusters and inter-cluster connections (12). Combined, this data indicated SH-SY5Y neuronal cultures exhibited a phenotype indicative of a stage of maturation between the hNSC H9 D15-18 and D60 time-point cultures.

Interestingly in ReNcell VMs, CD SDC3 was found to be upregulated in spontaneously differentiating cultures, while its MB and TMB forms were observed to be downregulated relative to basal conditions. This suggested intracellular signalling mediated by CD SDC3, to be particularly relevant during early lineage specification. The SDC3 CD interacts with cytoskeletal regulators and signalling proteins and is released via intramembrane proteolysis by the γ-secretase complex—an event that may interface with Notch intracellular signalling, which is known to influence neural development (59). Increased CD SDC3 levels in spontaneously differentiating ReNcell VM cultures may therefore reflect active Notch signalling—a pathway that must be suppressed for terminal differentiation to proceed (81). This is further supported by the observed elevated SDC3 expression during brain development in regions undergoing active neurogenesis and downregulated as neurons mature (69). Furthermore, along with the marked downregulation of CD SDC3 observed in SH-SY5Y-derived neuronal cultures, these cultures also exhibited more defined calcium oscillatory behaviour than ReNcell VM cells. Moreover, in ReNcell VM cultures treated with growth factors, the observed inverse relationship between calcium oscillation amplitude and SDC3 expression further suggested a regulatory role for SDC3 in the balance between progenitor maintenance and lineage commitment, potentially through the Notch pathway. This is further strengthened by the complete absence of both MB and CD SDC3 in astrocyte cultures.

Interestingly, the persistent, albeit reduced, expression of TMB SDC3 in the astrocyte cultures suggested a continued functional role for this isoform in astrocyte physiology. Prior studies have demonstrated that TMB SDC3—particularly its shed ectodomain—can modulate extracellular signalling dynamics, including interactions with growth factors and matrix components (82). Given the prominent role of astrocytes in secreting HS and PGs, it is plausible that TMB SDC3 remains expressed to support the regulated secretion of these molecules (83, 84). Notably, soluble SDC3 has also been implicated in the internalisation and fibrillation of α-synuclein—an event closely associated with neurodegenerative disease pathogenesis (85, 86). Further suggesting astrocytic preparation for HS secretion, we observed a marked shift in 10E4 staining patterns—from a diffuse distribution to distinct membrane clustering—indicating localised enrichment of HS. This change coincided with upregulation of HS biosynthetic enzymes EXT1, EXT2, and C5-EP, suggesting active elongation of HS chains. Interestingly, this also occurred alongside the downregulation of key sulfation enzymes such as NDST2, NDST4, and HS2ST1, while 6-O-sulfation and related modification enzymes activity was maintained. These selective changes in enzyme expression profiles may reflect a regulatory mechanism favouring dynamic remodelling and functional specificity of HS side chains in differentiated astrocytes.

As indicated previously, addition of PDGF to ReNcell VM neural inductive cultures appeared to suppress the astrocyte lineage and prompt oligodendrocyte lineages. This was shown by the significant downregulation observed for astrocyte markers GFAP, S100B, and SLC1A3, while O1 signal intensity was observed to increase. Interestingly, the expression of HSPGs remained unchanged in +PDGF cultures, apart from the upregulation of HS6ST1 and HPSE, further providing evidence for the importance of 6-O-sulfation and HS shedding in glial cells. Notably, HS was also increased in the neuronal SH-SY5Y cells, however there was a marked reduction in several N- and 6-O-sulfation enzymes along with increased SULF2 expression, further suggesting 6-O-sulfation patterns to be glial specific. SULF2 gene expression was also significantly upregulated in BDNF treated ReNcell VM cultures, suggesting BDNF increased the neuronal potential of the heterogenous ReNcell VM cells. In the mouse, Sulf2 has been shown to be required for neurite outgrowth (87) and neural fate decisions from motor neuron to oligodendrocytes through the Sonic Hedgehog (Shh) signalling pathway (88).

Interestingly, BDNF treatment also led to increased expression of GPC5 in ReNcell VM cultures. GPC5 has been shown to promote proliferation of mouse cerebellar granule cells by acting as a co-receptor for Shh signalling, particularly through its 2-O-sulfated HS residues (89). This upregulation correlated with the observed increase in cell numbers in BDNF-treated cultures, accompanied by decreased GPC6 expression. These findings suggest a possible functional divergence between the two GPCs, where GPC5 may support neuronal proliferation or maintenance, while GPC6 may be more relevant to astrocytic lineage commitment, consistent with its observed elevated expression in ReNcell CX-derived astrocyte cultures. Previous work by Allen et al. (2012) also identified GPC4 and GPC6 as astrocyte-secreted HSPGs involved in promoting synaptogenesis (90), while our previous work further established GPC4 as a key neural HSPG (12).

Most notably, the expression pattern of GPC2—also known as cerebroglycan—was particularly striking. Similar to SDC3, GPC2 exists in multiple isoforms. It is reported to be expressed in the adult brain and has been identified as a secreted marker of immature neurons in hNSC models (91). While the core protein of GPC2 is approximately 62 kDa, extensive glycosylation and HS chain modification increases its apparent molecular weight to ~100 kDa on an SDS-PAGE. This highly glycosylated form is enriched in neural tissues, where it plays a critical role in neuronal development, including cell adhesion and neurite outgrowth (92-94). In the present study, we observed marked upregulation of glycosylated GPC2 in differentiated SH-SY5Y and mixed-lineage ReNcell VM cultures. Interestingly, although to a lesser extent, glycosylated GPC2 was also seen to be elevated in ReNcell CX-derived astrocyte cultures. While modest, this expression suggests that post-translational modification of GPC2 may serve as a biomarker of lineage commitment within NPC-derived systems. These findings are consistent with reports showing dynamic modulation of GPC2 expression during neurodevelopment, where different isoforms may influence distinct stages of cell maturation (92).

Collectively, these results suggest that glycosylation of GPC2 enhanced its extracellular signalling capacity, particularly during lineage specification. The differential regulation of PG isoforms, including GPC2, underscored their complex and dynamic role in neural cell lineage fate processes. Future studies incorporating siRNA-mediated knockdown of GPC2 prior to differentiation could further elucidate its specific regulatory functions and potential as a target in modulating lineage outcomes.

5. Conclusions

This study revealed key insights into the dynamic regulation of HSPGs during neural lineage specification, with a particular emphasis on astrocytic lineage commitment. Although neither of the ReNcell models achieved full maturity or demonstrated homogeneous astrocyte cultures, ReNcell CXs most closely developed an astrocytic phenotype, while PDGF-treated ReNcell VMs exhibited a preferential bias toward an oligodendrocyte lineage. Notably, SDC3 emerged as a lineage-sensitive PG, with its cytoplasmic domain enriched in progenitor-like states and absent in inductive cultures—supporting its role in maintaining neural plasticity. In contrast, the persistence of TMB SDC3 in astrocyte cells suggests a continued role in modulating extracellular signalling and perhaps priming of the cells for increased HS and PG secretions, as shown by HS aggregations on the cell membrane. We showed that 6-O sulfation patterns may be relevant for glial lineages with PDGF treatment of ReNcell VM cultures with suppressed promotion of more oligodendrocyte-like features, confirming the capacity of the cells to bias glial lineage fate. Intriguingly, GPC2—a glycosylated neural proteoglycan—was upregulated in both neuronal and astrocytic cultures, indicating its potential as a post-translational biomarker of lineage progression. Together, these findings highlight distinct isoforms of SDC3 and GPC2 as central modulators of lineage specification in NPC-derived systems and underscore the utility of HSPG profiling in the refinement of human astrocyte model development.