Innovative Mitochondrial Isolation for Osteoarthritis Transplantation: Safety Profiles and Localization Outcomes In Vitro and In Vivo

1. Introduction

Osteoarthritis (OA) is a leading cause of impaired joint function and disability, associated with significant treatment costs and socio-economic burdens. Although current treatments for OA can improve symptoms, they do not inhibit the progression of the disease. In recent years, several research groups have focused their efforts on developing new treatments for OA, aiming to minimize pain, inflammation, and the degradation of articular tissues. Both in vitro and animal model studies of OA have shown promising results. However, few newly developed agents have successfully completed clinical trials [1], and OA treatment remains challenging, with no effective drugs currently available.

Mitochondrial dysfunction plays a crucial role in the pathogenesis of OA [2,3]. The term "transfer" refers to a process in which organelles are donated from one cell to another via various mechanisms [4,5,6]. Mitochondrial transfer may occur in response to a "help me" signal from a damaged cell [7,8], involving the formation of tunneling nanotubes or extracellular vesicles [9]. Intercellular organelle transfer has been described in both in vitro and in vivo model studies [10,11,12], suggesting that cell damage is critical in mitochondrial transfer in vivo [13]. The discovery of mitochondrial transfer has advanced treatments for mitochondrial dysfunction-related diseases and indicated its potential to restore function in damaged cells [8,14,15]. Mitochondrial transplantation involves augmenting or replacing damaged native mitochondria with viable mitochondria isolated from non-damaged tissue [16]. Studies in cell culture, isolated perfused organs, in vivo large animal models, and human clinical studies, suggested that mitochondrial transplantation is effective and safe [17,18,19,20].

Emerging evidence indicates that an imbalance in mitochondrial homeostasis contributes to the incidence and progression of OA [3,21,22,23]. A recent study suggested that bone marrow–derived mesenchymal stromal cells can be used to transfer mitochondria to murine OA chondrocytes, thereby enhancing ATP production [24]. Other studies have demonstrated that therapeutic interventions targeting mitochondria alleviate cartilage damage and OA symptoms [25], suggesting that the transfer of healthy mitochondria is a potentially beneficial strategy for treating OA [24,26]. Lee and coworkers examined the therapeutic potential of mitochondrial transplantation for treating OA in a rat model and reported that mitochondrial transplantation ameliorated OA progression and reduced pro-inflammatory changes [27].

However, none of these studies have investigated the fate of the transplanted mitochondria, whether they exit the joint and travel through the bloodstream to the liver or spleen, which specific tissues within the joint they integrate into, and if they do integrate, whether the mitochondria remain viable and functional, as well as the duration of their viability within the tissues.

A critical aspect of mitochondrial transplantation for disease treatment is the method of isolation. Standardizing a rapid, simple technique that ensures a high yield of viable mitochondria is essential. Various methods, often involving homogenization and/or differential centrifugation (DC), have been described, with earlier techniques forming the foundation of current practices [28,29].

Although DC-based methods are simple, they have several limitations, such as low purity of mitochondrial fractions [30]. Furthermore, DC protocols involve manual homogenization and repetitive steps that increase the time of isolation and the likelihood of mitochondrial damage, ultimately reducing mitochondrial viability [31]. The use of magnetic beads coupled to anti-TOM22 antibodies enables the isolation of highly pure functional mitochondria with minimal non-mitochondrial contamination [31,32,33]. The combined use of homogenization and DC to isolate mitochondria for transplantation into myocardial tissue has also been described [34,35]. This protocol requires less time and allows for uniform homogenization of the tissue, resulting in the isolation of highly purified and viable mitochondria.

In this project, we aim to develop and standardize a protocol for isolating high-quality, viable mitochondria specifically for application in articular tissues. Furthermore, we evaluate the safety and viability of administering isolated mitochondria into articular tissues and investigate the integration and distribution of transplanted mitochondria within joint tissues using both in vitro and in vivo models.

2. Materials and Methods

Animals

Animals were bred at the Experimental Surgery Unit of A Coruña under standard conditions. Animal experimentation was carried out in accordance with legislation regarding the protection of animals (European Directive 2010/63) used for scientific purposes and in compliance with the ARRIVE guidelines.

Mice

Twelve-week-old male C57BL/6JOlaHsd and NZB/OlaHsd mice (Mus musculus) strain were obtained from ENVIGO RMS. The mice were bred at the Experimental Surgery Unit of A Coruña under standard conditions, and food and water were provided ad libitum. After the experiments, the animals were sacrificed using carbon monoxide. The in vivo study was approved by the Local Ethical Committee of the Animal Experimentation “Comité de Ética de Experimentación Animal de la Xerencia de Xestión Integrada A Coruña (CEEA-XXIAC)” and by the “Consellería do Medio Rural” of Xunta de Galicia (15002/2022/004).

Piglets

Porcine cartilage and synovial membranes were obtained from joints of 3- to 4-month-old Large White pigs (Sus scrofa domestica) with a weight between 30-35 kg. Tissues were flushed with an antibiotic cocktail [penicillin (100 U/ml), streptomycin (100 μg/ml), amphotericin b (4 µg/ml), and gentamicin (4 µg/ml); (Sigma-Aldrich)] and then cultured for 24 h in Dulbecco Modified Eagle Medium (DMEM, Lonza) with 10% fetal bovine serum (FBS, Gibco) and antibiotic cocktail prior to the addition of mitochondria.

Isolation of Mitochondria

Mitochondria were isolated from mouse or piglet liver in function of the model. Briefly, a small piece of tissue was mechanically and enzymatically digested prior to application of the protocol described by Preble and coworkers [34], followed by magnetic purification using anti-TOM22 MicroBeads (Miltenyi Biotec) (Figure 1).

Tissue Dissociation and Differential Filtration

Tissue dissociation and differential filtration were carried out according to the protocol described by Preble [34], with some modifications. Briefly, liver tissue was preserved overnight (O/N) in phosphate-buffer-saline (PBS) supplemented with 10 mM EDTA (PBS+EDTA) (Sigma) at 4°C. The next day, a small piece (±0.35 g) was washed and minced (mechanical digestion). The tissue sample was then homogenized in 2× trypsin (Sigma-Aldrich) for 1 h on ice. The resulting digest was centrifuged at 300 g for 10 min, and the pellet was re-suspended in lysis buffer (Anti-TOM22 kit; Miltenyi Biotec) and applied to a dissociation C tube (Gentle MACS C tubes, Miltenyi Biotec). The tube was placed on the gentle MACS dissociator (Miltenyi Biotec), and the mitochondrial isolation cycle program was selected (3 × 60 s). The dissociation C tube was then moved to an ice bucket, and the resulting homogenate was filtered using a 40-μm mesh filter (Cultek). The elution product was used for the next step.

Isolation of Mitochondria Using Superparamagnetic Microbeads

An Anti-TOM22 MicroBeads kit (Miltenyi Biotec) was used for the magnetic isolation of mitochondria. Microbeads are a colloidal suspension of extremely small (i.e., 50-nm diameter) superparamagnetic particles conjugated to monoclonal anti-TOM22 antibodies. These microbeads were then used to magnetically isolate organelles using a MACS Separator.

The eluate obtained as described in the preceding section was incubated with 50 µl of anti-TOM22 MicroBeads and shaken for 1 h at 4°C. The suspension was loaded onto a pre-equilibrated MACS Column using a 30-µm filter provided with the kit (Miltenyi Biotec), which was placed in the magnetic field of a MACS Separator (Miltenyi Biotec). After removing the column from the magnetic field, retained mitochondria were eluted with 5 ml of elution buffer. Following centrifugation at 13,000 g for 5 min, the mitochondrial pellet was washed twice prior to resuspension in storage buffer.

Characterization of Isolated Mitochondria

Mitochondrial Protein Content

Total mitochondrial protein was obtained using 200 μl of M-PER™ Mammalian Protein Extraction Reagent (Thermo Fisher Scientific). The protein concentration was determined using a Bicinchoninic Acid (BCA) assay with a BCA Protein Assay kit (Pierce Biotechnology); using a Tecan Infinite M200 spectrophotometer NanoQuant (Tecan). For experiments, 14 or 28 µg of isolated mitochondria was used.

Mitochondrial Purity

Transmission electron microscopy (TEM). Mitochondrial purity and integrity were determined by TEM. Isolated mitochondria were fixed in 2.5% electron microscopy–grade glutaraldehyde in 0.1 M sodium cacodylate (pH 7.4) (Science Services) for at least 3 h, then washed 3 times for 5 min each in 0.1 M sodium cacodylate buffer. After, samples were post-fixed in 1% OsO4 in 0.1 M cacodylate for 1 h at room temperature (rt), dehydrated in a graded series of acetone, and embedded in Spurr’s resin (Taab). Semi-thin sections (1 µm thick) were cut using a Reichert-Jung ultramicrotome (Ultracut-E) and stained with toluidine blue and examined under a light microscope. Finally, ultra-thin sections (50–80 nm thick) were stained with uranyl acetate and lead citrate for 5 min and observed and photographed using a JEM1010 transmission electron microscope (Jeol) at 80 kV.

Western blotting (WB). Mitochondrial purity was evaluated by WB. Proteins were extracted from liver homogenate (Lv), the first elution from the magnetic column (Elt), and isolated mitochondria (Mit), using lysis buffer (6 M urea/2% SDS) and sonicated at 4°C. Protein concentrations were determined using the BCA assay and separated using SDS-PAGE, as previously described [36]. Separated proteins were then transferred onto membranes, which were incubated O/N at 4°C with the following antibodies: mouse anti–ATP synthase α (1:2000; Ab-612516 BD Bioscience), rabbit anti–GRP78 BiP (1:1000; Ab-108613 Abcam), and anti–α-tubulin (1:3000; Ab-T5168 Sigma-Aldrich). Anti-rabbit and anti-mouse secondary antibodies (1:1000; GE Healthcare) were used. ECL chemiluminescent substrate (Millipore) was used to detect antigen-antibody binding with an LAS-3000 luminescent image analyzer (Fujifilm).

Mitochondrial Viability

MitoTracker Red^®. Mitochondrial viability was assessed using MitoTracker Red CMXRos (ThermoFisher Scientific; ref M7512) (MitoTracker Red^®). Mitochondria were incubated with 250 nM MitoTracker Red® at 37°C for 30 minutes, washed three times with saline buffer, and a drop of the suspension was mounted on a slide with Prolong Gold Antifade Reagent. For the negative control the sobrenadant of MitoTracker Red® incubated without mitochondria was used (250 nM MitoTracker Red® was incubated in storage buffer without mitochondria and the same procedure described before was developed). Fluorescence was visualized and photographed with an Olympus BX61 microscope. Red fluorescence intensity was measured using a FACs Calibur flow cytometer. Data analysis was performed using CellQuest software.

ATP production. The metabolic activity of isolated mitochondria was evaluated by measuring ATP concentration using an ATP assay kit (Perkin Elmer) according to the manufacturer’s instructions. Mitochondria were incubated with 0.8 µM rotenone or antimycin A (Sigma) for 2 hours before ATP measurement. Luminescence was measured with a Nanoquant Infinite M200Pro (Tecan).

Mitochondrial Labeling

Cy5-labeled oligonucleotides. Cy5-labeled oligonucleotides were used to stain mitochondria within liver tissue. Oligo Cy5 at 50 nM was used as described by Lorenz and coworkers [37]. The protocol is described in Figure S1.

Iron oxide. Isolated mitochondria were incubated with iron oxide (II, III) magnetic nanopowder. A total of 10 mg of N-succinimidyl ester–functionalized, 30-nm magnetic iron (II, III) oxide particles (Sigma-Aldrich) was added to 14 µg of isolated mitochondria for 10 min at 0°C. The suspension was then washed 5 times in storage buffer. To confirm the presence of iron nanoparticles in the isolated mitochondria, TEM was performed, as described in section Mitochondrial purity.

MitoTracker Red^®. Isolated mitochondria were labeled with MitoTracker Red^®. Mitochondria were incubated in presence of MitoTracker Red^® at 37°C for 30 min. In parallel, a tube containing only storage buffer (without mitochondria) with MitoTracker Red^® was prepared as a negative control. The tubes were then washed 3 times by centrifugation at 13,000 rpm for 5 min.

Tissue samples containing; MitoTracker Red^®–labeled mitochondria and negative control (tissue incubated in presence of only storage buffer (without mitochondria) with MitoTracker Red^®) were embedded in Tissue-Tek^® optimum cutting temperature (OCT) compound (Sakura^® Finetek) and snap-frozen. The samples were then cryosectioned and fixed in 4% paraformaldehyde (Sigma-Aldrich) for 10 min at rt, followed by incubation in 0.1% Tween 20 (Sigma-Aldrich) for 5 min. The sections were then incubated for 5 min in a solution of Hoechst 33258 (Sigma-Aldrich) and washed with phosphate-buffer (PB). Cover slips were mounted on microscopy slides using Prolong Gold Antifade Reagent Mountant, and fluorescence was visualized and photographed under a Nikon AR-1 confocal microscope.

Mitochondrial Transplantation

In vitro models. Piglet cartilage and synovial membrane were isolated using a 5-mm punch biopsy. Explants were equilibrated in DMEM supplemented with 10% FBS, penicillin (100 U/ml), and streptomycin (100 μg/ml) (Gibco) in a humidified 5% CO2 atmosphere at 37°C. The next day, isolated mitochondria from piglet liver were labelled with MitoTracker Red^® or iron nanoparticles, and added over the explants. The tissues were then cultured. After incubation, the tissues were fixed in OCT, as described in section Mitochondrial labeling above. Tissues incubated with iron nanoparticle–labeled mitochondria were prepared for TEM by fixation in 2.5% electron microscopy–grade glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.4) (Science Services) for at least 6 h, then washed 3 times for 5 min each in 0.1 M sodium cacodylate buffer. The remaining steps were carried out as previously described in section Mitochondrial purity.

In Vivo Models

Short-term model. C57BL/6JOlaHsd male mice were used. Three experimental conditions were established, and all mice received an intraarticular injection in the left knee:

• Negative control group (Neg); mice were injected with vehicle (only isolation buffer).
• Fluorescence control group (Control); mice were injected with the supernadant obtained from isolation buffer (without mitochondria) incubated with MitoTracker Red^® following the same protocol that the Mito group.
• Injected mitochondria group (Mito); mice were injected in the joint isolated mitochondria in isolation buffer labeled with MitoTracker Red^®.

Forty-eight hours after injection, the animals were euthanized, and the knees and organs were collected, processed, and analyzed for MitoTracker Red® staining. Briefly, knee joints were fixed O/N in 3.7%–4% formaldehyde, decalcified by centrifugation in Decal (HistoLab) for 3 h at 200 rpm, and then subjected to paraffin embedding. Serial sections (4 μm) were cut, deparaffinized in xylene, and then subjected to a graded series of alcohol washes. The organs were fixed in OCT and processes as described above in section Mitochondrial labeling. Fluorescence was visualized and photographed under an Olympus microscope.

Long-term model. Healthy (without any surgery neither OA) male C57BL/6JOlaHsd mice received a single intraarticular injection of mitochondria obtained from C57BL/6JOlaHsd or NZB/OlaHsd mice to evaluate auto- and allogenic responses. Three experimental conditions were established and all mice in each group received an injection in the left knee. Mice were injected with isolated mitochondria obtained from C57BL/6JOlaHsd (Mitoc57) or NZB/OlaHsd (MitoNZB) mouse strains, and control mice were injected with vehicle (Control). After 7 weeks, the animals were sacrificed, and knee joints and organs were obtained and analyzed as described in the previous section Mitochondrial labeling. Body weight and joint width were measured weekly. Cartilage and synovial damage were assessed according to the Osteoarthritis Research Society International (OARSI) score [38] and Krenn classification [39,40] respectively.

Statistical Analyses

Data are presented as mean ± standard error of mean (SEM) from at least three independent experiments, with a minimum of three observations unless stated otherwise. Statistical analyses were performed using GraphPad Prism software, version 8.0.1. The unpaired nonparametric Mann-Whitney test was used to evaluate differences between experimental conditions. Differences with p values ≤ 0.05 were considered statistically significant.

3. Results

3.1. Characterization of Isolated Mitochondria

To determine if mitochondria remain viable when tissues from which they were isolated are preserved beforehand, liver specimens were kept O/N at 4°C in PBS+EDTA. Mitochondria were subsequently isolated, and their viability was assessed using MitoTracker Red®. The fluorescence intensity did not decrease over time in comparison with analysis of mitochondria obtained from fresh samples (Figure 2-A). Based on this result, the following experiments were performed with liver samples preserved O/N.

Mitochondrial viability was further evaluated by analyzing membrane potential using flow cytometry and measuring ATP production, confirming that the isolated mitochondria were functional. The measures evaluating mitochondrial membrane potential (Figure 2-B) and ATP production, and its reduction by inhibitors of the electron transport chain (Figure 2-C), indicated that the mitochondria were functional.

Mitochondrial purity was determined using transmission electron microscopy (TEM) and western blot (WB) (Figure 2-D-E). TEM images of isolated mitochondria are shown in Figure 2-D. Analysis of the purity of the mitochondrial fraction by WB showed that the isolated mitochondria had higher levels of ATP synthase α and lower levels of BIP (an endoplasmic reticulum marker) in comparison with protein fractions obtained from liver or the magnetic column eluate. In contrast, the cytoplasmic component tubulin-α was not detected in the mitochondrial fraction (Figure 2-E).

3.2. Mitochondrial Labeling

Isolated mitochondria were labeled using three different methodologies to determine the best option for subsequent analysis after transplantation in in vitro and in vivo models. In liver samples stained with Cy5-labeled oligonucleotides, the presence of Cy5 did not affect the tissue morphology and enabled labeling of the mitochondrial network within the tissue. However, fluorescence intensity decreased upon subsequent isolation of the mitochondria (Figure S1). Organelles were also labeled with iron nanoparticles or MitoTracker Red®, and microscopic evaluation showed positive signals in both cases (Figure 2-F). As a result, both stains were used for labeling isolated mitochondria in the following experiments.

3.3. Mitochondrial Administration in In Vitro Models

To evaluate the capacity of mitochondria to integrate into joint tissues, cartilage and synovial membrane explants were co-incubated with isolated mitochondria (14 µg) labeled with iron nanoparticles or MitoTracker Red®. Labeled mitochondria obtained from piglet liver were added to piglet cartilage and synovial membrane explants and incubated for 24 or 48 h (Figure 3-A). When tissues were incubated in presence of only storage buffer (without mitochondria) with MitoTracker Red^® (Negative control), no red fluorescence was detected (Figure 3-B-C). However, when tissues were co-cultured in the presence of isolated mitochondria, a fluorescence signal was observed and its intensity was maintained in both tissues for 24 and 48 h (Figure 3-B-C). Notably, analysis of cartilage images showed the presence of mitochondria in the superficial and intermediate layers (Figure 3-B).

Based on these data, we replicated the experiment, increasing the concentration of isolated mitochondria injected to 28 µg and the incubation time (Figure 4-A). Analysis of cartilage images indicated that viable mitochondria could be detected from 48 hours to 1 week after incubation (Figure 4-B). Mitochondria labeled with MitoTracker Red® in the synovial membrane were detected for up to 2 weeks (Figure 4-C).

To confirm the capacity of mitochondria to penetrate joint tissues, samples from the in vitro model were further analyzed using TEM with iron nanoparticle labeling. TEM analysis of cartilage without mitochondria did not show any mitochondria in the extracellular matrix (ECM) (Figure 5-A). TEM images of cartilage incubated for 48 hours with mitochondria showed the presence of isolated mitochondria in the superficial layer of the tissue, embedded in the ECM of the cartilage (Figure 5-B).

The capacity of isolated mitochondria to incorporate into the cells and ECM of the synovial membrane was also analyzed by microscopy. The morphology of the tissue and major cells, synoviocytes, was evaluated before mitochondrial injection and confirmed the absence of extracellular mitochondria in the ECM (Figure 5-C). Analysis of the synovium after 48 hours of incubation showed the presence of isolated mitochondria and iron nanoparticles in the ECM and within some synoviocytes (Figure 5-D).

3.4. Mitochondrial Injection in the Short-Term In Vivo Model

A short-term in vivo model was developed using C57BL/6JOlaHsd mice in which viable mitochondria labeled with MitoTracker Red® were injected into the left knee, and the animals were euthanized 48 hours later (Figure 6-A). To determine the location of the injected viable mitochondria in the joint, red fluorescence was analyzed in articular tissues. As shown in Figure 6-B-D, a noticeable red signal was detected in the superficial layer of the cartilage and in the synovial membrane compared to the negative control (vehicle-injected joint) or MitoTracker control (MitoTracker Red®–injected joint), in which no red fluorescence was detected. No infiltration of mitochondria was observed by monitoring red fluorescence in internal organs (Figure S2).

3.5. Mitochondrial Injection in the Long-Term In Vivo Model

To evaluate the long-term effects of intra-articular injection of mitochondria as well as allogeneic responses in the joint, C57BL/6JOlaHsd (autologous; Mitoc57) or NZB/OlaHsd (allogeneic; MitoNZB) mitochondria were injected into C57BL/6JOlaHsd mice (Figure 7-A). To assess model safety, body weight and joint width were measured weekly for 7 weeks, revealing that administration of C57BL/6JOlaHsd or NZB/OlaHsd mitochondria did not adversely affect these parameters relative to non-injected C57BL/6JOlaHsd (Control) mice (Figure 7-B-C). Internal organs were also analyzed and showed no detectable signs of damage (Figure S3). Evaluation of cartilage and synovial damage showed that injection of isolated mitochondria from the same or different strain induced neither pathological changes in the cartilage (Figure 7-D-E) nor synovial inflammation (Figure 7-F-G). These data indicate that the intra-articular injection of isolated mitochondria of autologous or allogeneic origin is safe in mice and does not damage the joint tissues or induce an inflammatory response in the joint.

4. Discussion

This study presents a novel approach utilizing intra-articular injection of isolated mitochondria. Our findings demonstrate the feasibility, safety, and potential therapeutic benefits of mitochondrial transplantation in joint tissues.

The first objective was to develop a robust protocol for isolating high-purity, viable mitochondria suitable for intra-articular transplantation. Numerous procedures have been described in the literature that involve various parameters affecting the quality and viability of isolated mitochondria [41,42]. We adopted and modified the procedure described by Preble and coworkers [34], combining mechanical and enzymatic digestion with magnetic purification using an-ti-TOM22 microbeads increasing the purity of mitochondria isolated. However, the method described here, slightly increases the time required for the isolation of mitochondria; however, the obtained mitochondria are viable and pure, which facilitates their use in mitochondrial injection, particularly in both in vivo and in vitro model.

This protocol allowed us to obtain isolated mitochondria with high viability after preserving the tissue overnight, thereby facilitating its implementation in clinical practice. This method allowed us to achieve mitochondria with high purity as evidenced by the lack of contamination with endoplasmic reticulum and cytosolic markers in the mitochondrial fractions. Transmission electron microscopy (TEM) and Western blot (WB) analyses confirmed the structural integrity and purity of the isolated mitochondria.

Several options are available for labeling isolated mitochondria. Oligonucleotides labeled with Cy5 or Cy3 have been utilized as mitochondrial markers in different cell lines but have not been previously used in tissues [37,43]. In our study, we demonstrated that Cy5-labeled oligonucleotides could effectively label mitochondria within the tissue; however, upon isolation from the tissue, the mitochondria exhibited low red fluorescence signals. Iron nanoparticles also offer a viable option for labeling mitochondria [44]. By labeling isolated mitochondria with 30-nm iron oxide particles, we obtained critical information regarding the distribution of transplanted mitochondria in joint tissue.

The functionality of the isolated mitochondria was rigorously tested through several assays. MitoTracker Red^® staining demonstrated that the mitochondria retained their membrane potential over time, indicating preserved viability. Additionally, ATP production assays confirmed the metabolic activity of the mitochondria, further supporting their functionality. These findings are crucial as they validate the use of these mitochondria for subsequent transplantation experiments.

Several authors have reported the successful transfer of exogenous mitochondria into cells or tissues, using MitoTracker dyes to trace these mitochondria within the recipient cells [45,46]. In this study, labeling mitochondria with MitoTracker has been utilized to confirm the internalization of exogenous mitochondria in various models [45,47]. In vitro experiments with piglet cartilage and synovial membrane explants provided valuable insights into the integration capabilities of the isolated mitochondria. When co-cultured with mitochondria labeled with MitoTracker Red® or iron nanoparticles, the explants exhibited significant fluorescence signals, indicating successful incorporation of mitochondria into the superficial and intermediate layers of cartilage as well as the synovial membrane. TEM analysis further corroborated these findings, showing mitochondria embedded in the extracellular matrix (ECM) and within synoviocytes.

In the short-term in vivo model, intra-articular injection of MitoTracker Red®-labeled mitochondria resulted in detectable red fluorescence in the superficial layer of cartilage and the synovial membrane 48 hours post-injection. Importantly, no red fluorescence was observed in internal organs, suggesting that the mitochondria remained localized within the joint. This localization is critical for minimizing potential systemic effects and maximizing therapeutic efficacy.

Previous studies have shown a lack of immune response following the injection of autogenetic and allogeneic mitochondria [48,49,50]. To assess the long-term safety and potential allogeneic responses, we injected mitochondria isolated from both autologous (C57BL/6JOlaHsd) and allogeneic (NZB/OlaHsd) sources into C57BL/6JOlaHsd mice. Over a seven-week period, no adverse effects on body weight or joint width were observed, and there were no signs of damage in internal organs. Histological analyses revealed no pathological changes in cartilage or synovial tissue, indicating that the intra-articular injection of mitochondria, whether autologous or allogeneic, is safe and does not induce inflammatory responses in the joint.

5. Conclusions

This study establishes foundational protocol for functional mitochondrial isolation and demonstrates that isolated mitochondria can penetrate the various tissues that constitute the joint, as demonstrated by our in vitro experiments. In vivo, isolated mitochondria injected into the joint penetrated the superficial layer of cartilage and the synovial membrane, remaining in the joint for at least 48 hours post-injection. Additionally, this study indicates that mitochondrial injection is safe, does not damage the cartilage or synovium, and does not cause systemic toxicity. These findings support the potential of mitochondrial transplantation as a therapeutic strategy for OA as well as other diseases with mitochondrial dysfunction. However, further studies are necessary to elucidate the long-term effects of mitochondrial transplantation, optimal dosing strategies, and the underlying mechanisms by which transplanted mitochondria may confer therapeutic benefits.