Histological Effects of Mesenchymal Stem Cell Therapy on Cartilage Repair in Osteoarthritis: A Scoping Review

Authors

DOI:

https://doi.org/10.65745/soj.v1.i2.15

Keywords:

mesenchymal stem cell, osteoarthritis, cartilage repair, histology

Abstract

Osteoarthritis (OA) is a chronic joint disease characterized by pain, stiffness, and progressive functional impairment. Mesenchymal stem cell (MSC) therapy has emerged as a potential approach to promoting cartilage repair; however, its histological effects require further evaluation. This scoping review aimed to map and synthesize evidence on the histological effects of MSC therapy in OA. The review followed the PRISMA Extension for Scoping Reviews (PRISMA-ScR) guidelines. Literature searches were conducted from November to December 2024 across six databases: ScienceDirect, SpringerLink, ProQuest, EBSCO, MEDLINE, and Cochrane. The search strategy was developed using the PICO framework and relevant Boolean operators. Of 3,184 records identified, 26 studies met the inclusion criteria. Twenty-one studies reported improvements in cartilage-related histological parameters, including chondrocyte volume or cartilage density. Six studies described favorable changes in chondrocyte characteristics, including reduced apoptosis and hypertrophy. Fourteen studies reported improvements in extracellular matrix composition, particularly increased type II collagen (COL2) and decreased type I collagen (COL1) expression. Seven studies identified immunomodulatory effects, including reduced pro-inflammatory or increased anti-inflammatory cytokine levels. Only one study reported no statistically significant difference between MSC-treated and control groups. Overall, the available evidence suggests that MSC therapy may promote cartilage repair through structural, cellular, extracellular matrix, and immunomodulatory mechanisms. However, heterogeneity across studies and the limited comparability of histological outcomes prevent definitive conclusions. Further research is needed to standardize MSC administration protocols and evaluate treatment responses under varying inflammatory conditions.

References

Alcaide-Ruggiero, L., Molina-Hernández, V., Granados, M. M., & Domínguez, J. M. (2021). Main and Minor Types of Collagens in the Articular Cartilage: The Role of Collagens in Repair Tissue Evaluation in Chondral Defects. International Journal of Molecular Sciences, 22(24), 13329. https://doi.org/10.3390/ijms222413329

Armstrong, A. R., Carlson, C. S., Rendahl, A. K., & Loeser, R. F. (2021). Optimization of histologic grading schemes in spontaneous and surgically-induced murine models of osteoarthritis. Osteoarthritis and Cartilage, 29(4), 536–546. https://doi.org/10.1016/j.joca.2021.01.006

Bačenková, D., Trebuňová, M., Demeterová, J., & Živčák, J. (2023). Human Chondrocytes, Metabolism of Articular Cartilage, and Strategies for Application to Tissue Engineering. International Journal of Molecular Sciences, 24(23), 17096. https://doi.org/10.3390/ijms242317096

Beerts, C., Broeckx, S. Y., Depuydt, E., Tack, L., Van Hecke, L., Chiers, K., Van Brantegem, L., Braun, G., Hellmann, K., De Bouvre, N., Van Bruaene, N., De Ryck, T., Duchateau, L., Van Ryssen, B., Peremans, K., Saunders, J. H., Verhoeven, G., Pauwelyn, G., & Spaas, J. H. (2023). Low-dose xenogeneic mesenchymal stem cells target canine osteoarthritis through systemic immunomodulation and homing. Arthritis Research & Therapy, 25(1), 190. https://doi.org/10.1186/s13075-023-03168-7

Boraschi, D. (2022). What Is IL-1 for? The Functions of Interleukin-1 Across Evolution. Frontiers in Immunology, 13, 872155. https://doi.org/10.3389/fimmu.2022.872155

Butarbutar, J. Cp., Basuki, P., Sungono, V., Riantho, A., & Fidiasrianto, K. (2024). Burden of osteoarthritis in Indonesia: A Global Burden of Disease (GBD) study 2019. Narra J, 4(2), e884. https://doi.org/10.52225/narra.v4i2.884

Chang, Y.-H., Wu, K.-C., Hsu, C.-J., Tu, T.-C., Liu, M.-C., Chiang, R. Y.-S., & Ding, D.-C. (2024).Therapeutic Potential of Olfactory Ensheathing Cells and Adipose-Derived Stem Cells in Osteoarthritis: Insights from Preclinical Studies. Cells, 13(15), 1250. https://doi.org/10.3390/cells13151250

Chavda, S., Rabbani, S. A., & Wadhwa, T. (2022). Role and Effectiveness of Intra-articular Injection of Hyaluronic Acid in the Treatment of Knee Osteoarthritis: A Systematic Review. Cureus. https://doi.org/10.7759/cureus.24503

Chawla, S., Mainardi, A., Majumder, N., Dönges, L., Kumar, B., Occhetta, P., Martin, I., Egloff, C., Ghosh, S., Bandyopadhyay, A., & Barbero, A. (2022). Chondrocyte Hypertrophy in Osteoarthritis: Mechanistic Studies and Models for the Identification of New Therapeutic Strategies. Cells, 11(24), 4034. https://doi.org/10.3390/cells11244034

Chu, H., Zhang, S., Zhang, Z., Yue, H., Liu, H., Li, B., & Yin, F. (2024). Comparison studies identify mesenchymal stromal cells with potent regenerative activity in osteoarthritis treatment. Npj Regenerative Medicine, 9(1), 14. https://doi.org/10.1038/s41536-024-00358-y

Coaccioli, S., Sarzi-Puttini, P., Zis, P., Rinonapoli, G., & Varrassi, G. (2022). Osteoarthritis: New Insight on Its Pathophysiology. Journal of Clinical Medicine, 11(20), 6013. https://doi.org/10.3390/jcm11206013

Deng, Z., Zeng, X., Lin, B., Chen, L., Wu, J., Zheng, J., Ma, Y., Lyu, F.-J., & Zheng, Q. (2024). Human umbilical cord mesenchymal stem cells on treating osteoarthritis in a rabbit model: Injection strategies. Heliyon, 10(19), e38384. https://doi.org/10.1016/j.heliyon.2024.e38384

Esquivel, D., Mishra, R., & Srivastava, A. (2024). Potential use of stem cell therapies for treating osteoarthritis and rheumatoid arthritis. Annals of Translational Medicine, 12(4), 72–72. https://doi.org/10.21037/atm-23-1951

Ferreira, R. M., Martins, P. N., & Gonçalves, R. S. (2024). Non-pharmacological and non-surgical interventions to manage patients with knee osteoarthritis: An umbrella review 5-year update. Osteoarthritis and Cartilage Open, 6(3). https://doi.org/10.1016/j.ocarto.2024.100497

Gherghel, R., Macovei, L. A., Burlui, M.-A., Cardoneanu, A., Rezus, I.-I., Mihai, I. R., & Rezus, E. (2023). Osteoarthritis—The Role of Mesenchymal Stem Cells in Cartilage Regeneration. Applied Sciences, 13(19), 10617. https://doi.org/10.3390/app131910617

Gugjoo, M. B., Dar, E. R., Farooq, F., Ahmad, S. M., Sofi, A. H., Shah, S. A., Bhat, M. H., Khan, T. A., Shah, R. A., & Parrah, J.-U.-D. (2023). Cryopreserved allogeneic bone marrow mesenchymal stem cells show better osteochondral defect repair potential than adipose tissue mesenchymal stem cells. Current Research in Translational Medicine, 71(1), 103364. https://doi.org/10.1016/j.retram.2022.103364

Guo, X., Xi, L., Yu, M., Fan, Z., Wang, W., Ju, A., Liang, Z., Zhou, G., & Ren, W. (2023). Regeneration of articular cartilage defects: Therapeutic strategies and perspectives. Journal of Tissue Engineering, 14, 20417314231164765. https://doi.org/10.1177/20417314231164765

Hamdalla, H. M., Ahmed, R. R., Galaly, S. R., Ahmed, O. M., Naguib, I. A., Alghamdi, B. S., & Abdul-Hamid, M. (2022). Assessment of the Efficacy of Bone Marrow-Derived Mesenchymal Stem Cells against a Monoiodoacetate-Induced Osteoarthritis Model in Wistar Rats. Stem Cells International, 2022, 1–14. https://doi.org/10.1155/2022/1900403

Han, Y., Li, H., Zhou, R., Wu, J., Liu, Z., Wang, H., Shao, J., Chen, Y., Zhu, J., Fu, Q., Qian, Q., & Zhou, Y. (2021). Comparison between Intra-Articular Injection of Infrapatellar Fat Pad (IPFP) Cell Concentrates and IPFP-Mesenchymal Stem Cells (MSCs) for Cartilage Defect Repair of the Knee Joint in Rabbits. Stem Cells International, 2021(1), 9966966. https://doi.org/10.1155/2021/9966966

Hellmi, R. Y., Najirman, Manuaba, IA. R. W., Rahmadi, A. R., Kurniari, P. K., Chair, M., Warlisti, I. V., Kurniawan, E., Isbagio, H., Kalim, H., Hidayat, R., Hamijoyo, L., Wahono, C. S., & Sumariyono. (2023). Diagnosis dan Pengelolaan Osteoartritis (Lutut, Tangan, dan Panggul). Perhimpunan Reumatologi Indonesia. https://reumatologi.or.id/wp-content/uploads/2023/03/Rekomendasi-OSTEOARTRI TIS-PBIRA.pdf

Ju, Y., Yi, L., Li, C., Wang, T., Zhang, W., Chai, W., Yin, X., & Weng, T. (2022). Comparison of biological characteristics of human adipose- and umbilical cord- derived mesenchymal stem cells and their effects on delaying the progression of osteoarthritis in a rat model. Acta Histochemica, 124(6), 151911. https://doi.org/10.1016/j.acthis.2022.151911

Kaeppler, E. P. von, Wang, Q., Raghu, H., Bloom, M. S., Wong, H., & Robinson, W. H. (2021). Interleukin 4 promotes anti-inflammatory macrophages that clear cartilage debris and inhibits osteoclast development to protect against osteoarthritis. Clinical Immunology, 229, 108784. https://doi.org/10.1016/j.clim.2021.108784

Kim, H., Yang, G., Park, J., Choi, J., Kang, E., & Lee, B.-K. (2019). Therapeutic effect of mesenchymal stem cells derived from human umbilical cord in rabbit temporomandibular joint model of osteoarthritis. Scientific Reports, 9(1), 13854. https://doi.org/10.1038/s41598-019-50435-2

Kim, Y. S., Kim, Y. I., & Koh, Y. G. (2021). Intra-articular injection of human synovium-derived mesenchymal stem cells in beagles with surgery-induced osteoarthritis. The Knee, 28, 159–168. https://doi.org/10.1016/j.knee.2020.11.021

Kolasinski, S. L., Neogi, T., Hochberg, M. C., Oatis, C., Guyatt, G., Block, J., Callahan, L., Copenhaver, C., Dodge, C., Felson, D., Gellar, K., Harvey, W. F., Hawker, G., Herzig, E., Kwoh, C. K., Nelson, A. E., Samuels, J., Scanzello, C., White, D., … Reston, J. (2020). 2019 American College of Rheumatology/Arthritis Foundation Guideline for the Management of Osteoarthritis of the Hand, Hip, and Knee. Arthritis & Rheumatology, 72(2), 220–233. https://doi.org/10.1002/art.41142

Krawetz, R. J., Larijani, L., Corpuz, J. M., Ninkovic, N., Das, N., Olsen, A., Mohtadi, N., Rezansoff, A., & Dufour, A. (2023). Mesenchymal progenitor cells from non-inflamed versus inflamed synovium post-ACL injury present with distinct phenotypes and cartilage regeneration capacity. Stem Cell Research & Therapy, 14(1), 168. https://doi.org/10.1186/s13287-023-03396-3

Kumar, V., Abbas, A. K., Aster, J. C., Deyrup, A. T., & Das, A. (2023). Robbins & Kumar Basic Pathology (11th edn). Elsevier. https://books.google.co.id/books?id=LVMG0AEACAAJ

Lee, Y. T., Mohd Yunus, M. H., Yazid, M. D., & Ugusman, A. (2024). Unraveling the path to osteoarthritis management: Targeting chondrocyte apoptosis for therapeutic intervention. Frontiers in Cell and Developmental Biology, 12, 1347126. https://doi.org/10.3389/fcell.2024.1347126

Li, P.-L., Wang, Y.-X., Zhao, Z.-D., Li, Z.-L., Liang, J.-W., Wang, Q., Yin, B.-F., Hao, R.-C., Han, M.-Y., Ding, L., Wu, C.-T., & Zhu, H. (2021). Clinical-grade human dental pulp stem cells suppressed the activation of osteoarthritic macrophages and attenuated cartilaginous damage in a rabbit osteoarthritis model. Stem Cell Research & Therapy, 12(1), 260. https://doi.org/10.1186/s13287-021-02353-2

Li, Z., Huang, Z., & Bai, L. (2021). Cell Interplay in Osteoarthritis. Frontiers in Cell and Developmental Biology, 9, 720477. https://doi.org/10.3389/fcell.2021.720477

Li, Z.-L., Li, X.-T., Hao, R.-C., Wang, F.-Y., Wang, Y.-X., Zhao, Z.-D., Li, P.-L., Yin, B.-F., Mao, N., Ding, L., & Zhu, H. (2023). Human osteoarthritic articular cartilage stem cells suppress osteoclasts and improve subchondral bone remodeling in experimental knee osteoarthritis partially by releasing TNFAIP3. Stem Cell Research & Therapy, 14(1), 253. https://doi.org/10.1186/s13287-023-03411-7

Liao, Y., Ren, Y., Luo, X., Mirando, A. J., Long, J. T., Leinroth, A., Ji, R.-R., & Hilton, M. J. (2022). Interleukin-6 signaling mediates cartilage degradation and pain in posttraumatic osteoarthritis in a sex-specific manner. Science Signaling, 15(744), eabn7082. https://doi.org/10.1126/scisignal.abn7082

Lin, S.-C., Panthi, S., Hsuuw, Y.-H., Chen, S.-H., Huang, M.-J., Sieber, M., & Hsuuw, Y.-D. (2023). Regenerative Effect of Mesenchymal Stem Cell on Cartilage Damage in a Porcine Model. Biomedicines, 11(7), 1810.

https://doi.org/10.3390/biomedicines11071810

Loo, S., & Wong, N. (2021). Advantages and challenges of stem cell therapy for osteoarthritis (Review). Biomedical Reports, 15(2), 67.

https://doi.org/10.3892/br.2021.1443

Mak, S., & Thomas, A. (2022). Steps for Conducting a Scoping Review. Journal of Graduate Medical Education, 14(5), 565–567. https://doi.org/10.4300/JGME-D-22-00621.1

Maldonado, M., & Nam, J. (2013). The Role of Changes in Extracellular Matrix of Cartilage in the Presence of Inflammation on the Pathology of Osteoarthritis. BioMed Research International, 2013, 1–10. https://doi.org/10.1155/2013/284873

Mancuso, P., Raman, S., Glynn, A., Barry, F., & Murphy, J. M. (2019). Mesenchymal Stem Cell Therapy for Osteoarthritis: The Critical Role of the Cell Secretome. Frontiers in Bioengineering and Biotechnology, 7, 9. https://doi.org/10.3389/fbioe.2019.00009

Molnar, V., Matišić, V., Kodvanj, I., Bjelica, R., Jeleč, Ž., Hudetz, D., Rod, E., Čukelj, F., Vrdoljak, T., Vidović, D., Starešinić, M., Sabalić, S., Dobričić, B., Petrović, T., Antičević, D., Borić, I., Košir, R., Zmrzljak, U. P., & Primorac, D. (2021). Cytokines and Chemokines Involved in Osteoarthritis Pathogenesis. International Journal of Molecular Sciences, 22(17), 9208. https://doi.org/10.3390/ijms22179208

Ni, S., Shan, F., & Geng, J. (2022). Interleukin-10 family members: Biology and role in the bone and joint diseases. International Immunopharmacology, 108, 108881.

https://doi.org/10.1016/j.intimp.2022.108881

Ogasawara, N., Kano, F., Hashimoto, N., Mori, H., Liu, Y., Xia, L., Sakamaki, T., Hibi, H., Iwamoto, T., Tanaka, E., & Yamamoto, A. (2020). Factors secreted from dental pulp stem cells show multifaceted benefits for treating experimental temporomandibular joint osteoarthritis. Osteoarthritis and Cartilage, 28(6), 831–841. https://doi.org/10.1016/j.joca.2020.03.010

Oliveira, F. B. D. D., Antonioli, E., Dias, O. F. M., Souza, J. G. D., Agarwal, S., Chudzinski-Tavassi, A. M., & Ferretti, M. (2023). Comparative Effects of Intra-Articular versus Intravenous Mesenchymal Stromal Cells Therapy in a Rat Model of Osteoarthritis by Destabilization of Medial Meniscus. International Journal of Molecular Sciences, 24(21), 15543.

https://doi.org/10.3390/ijms242115543

Ouyang, Z., Dong, L., Yao, F., Wang, K., Chen, Y., Li, S., Zhou, R., Zhao, Y., & Hu, W. (2023). Cartilage-Related Collagens in Osteoarthritis and Rheumatoid Arthritis: From Pathogenesis to Therapeutics. International Journal of Molecular Sciences, 24(12), 9841. https://doi.org/10.3390/ijms24129841

Page, M. J., Moher, D., Bossuyt, P. M., Boutron, I., Hoffmann, T. C., Mulrow, C. D., Shamseer, L., Tetzlaff, J. M., Akl, E. A., Brennan, S. E., Chou, R., Glanville, J., Grimshaw, J. M., Hróbjartsson, A., Lalu, M. M., Li, T., Loder, E. W., Mayo-Wilson, E., McDonald, S., … McKenzie, J. E. (2021). PRISMA 2020 explanation and elaboration: Updated guidance and exemplars for reporting systematic reviews. BMJ, n160. https://doi.org/10.1136/bmj.n160

Pritzker, K. P. H., Gay, S., Jimenez, S. A., Ostergaard, K., Pelletier, J.-P., Revell, P. A., Salter, D., & Berg, W. B. van den. (2006). Osteoarthritis cartilage histopathology: Grading and staging. Osteoarthritis and Cartilage, 14(1), 13–29. https://doi.org/10.1016/j.joca.2005.07.014

Puhakka, J., Salonius, E., Paatela, T., Muhonen, V., Meller, A., Vasara, A., Kautiainen, H., Kosola, J., & Kiviranta, I. (2022). Comparison Between Arthroscopic and Histological International Cartilage Repair Society Scoring Systems in Porcine Cartilage Repair Model. CARTILAGE, 13(1), 19476035211069246. https://doi.org/10.1177/19476035211069246

Ragni, E., Colombini, A., Viganò, M., Libonati, F., Perucca Orfei, C., Zagra, L., & De Girolamo, L. (2021). Cartilage Protective and Immunomodulatory Features of Osteoarthritis Synovial Fluid-Treated Adipose-Derived Mesenchymal Stem Cells Secreted Factors and Extracellular Vesicles-Embedded miRNAs. Cells, 10(5), 1072.

https://doi.org/10.3390/cells10051072

Rapp, A. E., & Zaucke, F. (2023). Cartilage extracellular matrix-derived matrikines in osteoarthritis. American Journal of Physiology-Cell Physiology, 324(2), C377–C394. https://doi.org/10.1152/ajpcell.00464.2022

Rowden, A. (2024, May 30). Surgery for osteoarthritis: Types, benefits, risks, and more.

MedicalNewsToday. https://www.medicalnewstoday.com/articles/surgery-for-osteoarthritis

Sahin, N., & Yesil, H. (2023). Regenerative methods in osteoarthritis. Best Practice & Research Clinical Rheumatology, Osteoarthritis, 37(2), 101824.

https://doi.org/10.1016/j.berh.2023.101824

Samvelyan, H. J., Hughes, D., Stevens, C., & Staines, K. A. (2021). Models of Osteoarthritis: Relevance and New Insights. Calcified Tissue International, 109(3), 243–256. https://doi.org/10.1007/s00223-020-00670-x

Satué, M., Schüler, C., Ginner, N., & Erben, R. G. (2019). Intra-articularly injected mesenchymal stem cells promote cartilage regeneration, but do not permanently engraft in distant organs. Scientific Reports, 9(1), 10153. https://doi.org/10.1038/s41598-019-46554-5

Sen, R., & Hurley, J. A. (2026). Osteoarthritis. In StatPearls. StatPearls Publishing. http://www.ncbi.nlm.nih.gov/books/NBK482326/

Sengprasert, P., Kamenkit, O., Tanavalee, A., & Reantragoon, R. (2024). The Immunological Facets of Chondrocytes in Osteoarthritis: A Narrative Review. The Journal of Rheumatology, 51(1), 13–24. https://doi.org/10.3899/jrheum.2023-0816

Sherman, M. S., McMahon-Skates, T., Gaston, L. S., Katzen, S. W., Majzoub, J. A., & Goessling, W. (2025). Harmonizing TUNEL with multiplexed iterative immunofluorescence enriches spatial contextualization of cell death. Cell Reports Methods, 5(5). https://doi.org/10.1016/j.crmeth.2025.101047

Shoukrie, S. I., Venugopal, S., Dhanoa, R. K., Selvaraj, R., Selvamani, T. Y., Zahra, A., Malla, J., Hamouda, R. K., & Hamid, P. F. (2022). Safety and Efficacy of Injecting Mesenchymal Stem Cells Into a Human Knee Joint To Treat Osteoarthritis: A Systematic Review. Cureus. https://doi.org/10.7759/cureus.24823

Steinmetz, J. D., Culbreth, G. T., Haile, L. M., Rafferty, Q., Lo, J., Fukutaki, K. G., Cruz, J. A.,Smith, A. E., Vollset, S. E., Brooks, P. M., Cross, M., Woolf, A. D., Hagins, H., Abbasi-Kangevari, M., Abedi, A., Ackerman, I. N., Amu, H., Antony, B., Arabloo, J., … Kopec, J. A. (2023). Global, regional, and national burden of osteoarthritis, 1990–2020 and projections to 2050: A systematic analysis for the Global Burden of

Disease Study 2021. The Lancet Rheumatology, 5(9), e508–e522. https://doi.org/10.1016/S2665-9913(23)00163-7

Tang, S., Chen, P., Zhang, H., Weng, H., Fang, Z., Chen, C., Peng, G., Gao, H., Hu, K., Chen, J., Chen, L., & Chen, X. (2021). Comparison of Curative Effect of Human Umbilical Cord-Derived Mesenchymal Stem Cells and Their Small Extracellular Vesicles in Treating Osteoarthritis. International Journal of Nanomedicine, Volume 16, 8185–8202. https://doi.org/10.2147/IJN.S336062

Thoene, M., Bejer-Olenska, E., & Wojtkiewicz, J. (2023). The Current State of Osteoarthritis Treatment Options Using Stem Cells for Regenerative Therapy: A Review. International Journal of Molecular Sciences, 24(10), 8925. https://doi.org/10.3390/ijms24108925

Tian, X., Qu, Z., Cao, Y., & Zhang, B. (2024). Relative efficacy and safety of mesenchymal stem cells for osteoarthritis: A systematic review and meta-analysis of randomized controlled trials. Frontiers in Endocrinology, 15, 1366297. https://doi.org/10.3389/fendo.2024.1366297

Tong, Z., Yang, X., & Li, J. (2022). Research progress on the mechanism of interleukin-1β on epiphyseal plate chondrocytes. European Journal of Medical Research, 27(1), 313. https://doi.org/10.1186/s40001-022-00893-8

Ukai, T., Sato, M., Wasai, S., Takahashi, T., Omura, H., & Watanabe, M. (2021). Comparison of properties determined using electromechanical assessment (Arthro-BSTTM) with macroscopic and histological properties in symptomatic human articular cartilage of the hip. Arthritis Research & Therapy, 23(1), 227. https://doi.org/10.1186/s13075-021-02611-x

Verdejo, C., Tapia-Benavente, L., Schuller-Martínez, B., Vergara-Merino, L., Vargas-Peirano, M., & Silva-Dreyer, A. M. (2021, March 30). What you need to know about scoping reviews. Medwave.

https://www.medwave.cl/revisiones/metodinvestreport/8144.html

Wang, Y., Fan, M., Wang, H., You, Y., Wei, C., Liu, M., Luo, A., Xu, X., & Duan, X. (2022). Relative safety and efficacy of topical and oral NSAIDs in the treatment of osteoarthritis: A systematic review and meta-analysis. Medicine, 101(36), e30354. https://doi.org/10.1097/MD.0000000000030354

Warmink, K., Rios, J. L., Varderidou-Minasian, S., Torres-Torrillas, M., Van Valkengoed, D. R., Versteeg, S., Eijkelkamp, N., Weinans, H., Korthagen, N. M., & Lorenowicz, M. J. (2023). Mesenchymal stem/stromal cells-derived extracellular vesicles as a potentially more beneficial therapeutic strategy than MSC-based treatment in a mild metabolic osteoarthritis model. Stem Cell Research & Therapy, 14(1), 137. https://doi.org/10.1186/s13287-023-03368-7

Wiegertjes, R., Van De Loo, F. A. J., & Blaney Davidson, E. N. (2020). A roadmap to target interleukin-6 in osteoarthritis. Rheumatology, 59(10), 2681–2694. https://doi.org/10.1093/rheumatology/keaa248

World Health Organization. (2023, July 14). Osteoarthritis. Who.Int. https://www.who.int/news-room/fact-sheets/detail/osteoarthritis

Wu, J., Huang, S., Yu, Y., Lian, Q., Liu, Y., Dai, W., Liu, Q., Pan, Y., Liu, G., Li, K., Liu, C., & Li, G. (2024). Human adipose and synovial-derived MSCs synergistically attenuate osteoarthritis by promoting chondrocyte autophagy through FoxO1 signaling. Stem Cell Research & Therapy, 15(1), 261. https://doi.org/10.1186/s13287-024-03870-6

Xiang, X.-N., Zhu, S.-Y., He, H.-C., Yu, X., Xu, Y., & He, C.-Q. (2022). Mesenchymal stromal cell-based therapy for cartilage regeneration in knee osteoarthritis. Stem Cell Research & Therapy, 13(1), 14. https://doi.org/10.1186/s13287-021-02689-9

Xing, D., Wang, K., Wu, J., Zhao, Y., Liu, W., Li, J. J., Gao, T., Yan, D., Wang, L., Hao, J., & Lin, J. (2021). Clinical-Grade Human Embryonic Stem Cell-Derived Mesenchymal Stromal Cells Ameliorate the Progression of Osteoarthritis in a Rat Model. Molecules, 26(3), 604. https://doi.org/10.3390/molecules26030604

Xing, D., Wu, J., Wang, B., Liu, W., Liu, W., Zhao, Y., Wang, L., Li, J. J., Liu, A., Zhou, Q., Hao, J., & Lin, J. (2020). Intra-articular delivery of umbilical cord-derived mesenchymal stem cells temporarily retard the progression of osteoarthritis in a rat model. International Journal of Rheumatic Diseases, 23(6), 778–787. https://doi.org/10.1111/1756-185X.13834

Yao, Q., Wu, X., Tao, C., Gong, W., Chen, M., Qu, M., Zhong, Y., He, T., Chen, S., & Xiao, G. (2023). Osteoarthritis: Pathogenic signaling pathways and therapeutic targets. Signal Transduction and Targeted Therapy, 8(1), 56. https://doi.org/10.1038/s41392-023-01330-w

Yunus, M. H. M., Nordin, A., & Kamal, H. (2020). Pathophysiological Perspective of Osteoarthritis. Medicina, 56(11), 614. https://doi.org/10.3390/medicina56110614

Zare, R., Tanideh, N., Nikahval, B., Mirtalebi, M. S., Ahmadi, N., Zarea, S., Hosseinabadi, O. K., Bhimani, R., & Ashkani-Esfahani, S. (2020). Are Stem Cells Derived from Synovium and Fat Pad Able to Treat Induced Knee Osteoarthritis in Rats? International Journal of Rheumatology, 2020, 1–8. https://doi.org/10.1155/2020/9610261

Zhang, Y., He, X., Ge, Z., Wang, B., Ni, M., & Cai, G. (2024). Investigating the differential therapeutic efficacy and mechanisms of human umbilical cord mesenchymal stem cells at various passages in osteoarthritis treatment. Tissue and Cell, 90, 102499. https://doi.org/10.1016/j.tice.2024.102499

Zhao, S., Liu, Y., Wang, J., Wen, Y., Wu, B., Yang, D., Wang, G., Xiu, G., Ling, B., Du, D., & Xu, J. (2023). ADSCs increase the autophagy of chondrocytes through decreasing miR-7-5p in Osteoarthritis rats by targeting ATG4A. International Immunopharmacology, 120, 110390. https://doi.org/10.1016/j.intimp.2023.110390

Published

2026-11-02

Issue

Section

Articles

How to Cite

Zulfah Zahrah, Z., & Sulistyoningrum, E. . (2026). Histological Effects of Mesenchymal Stem Cell Therapy on Cartilage Repair in Osteoarthritis: A Scoping Review. Soeharso Orthopaedic Journal, 1(2). https://doi.org/10.65745/soj.v1.i2.15