Phenotype Diversity of Macrophages in Osteoarthritis: Implications for Development of Macrophage Modulating Therapies
- PMID: 35955514
- PMCID: PMC9369350
- DOI: 10.3390/ijms23158381
Phenotype Diversity of Macrophages in Osteoarthritis: Implications for Development of Macrophage Modulating Therapies
Abstract
Chronic inflammation is implicated in numerous human pathologies. In particular, low-grade inflammation is currently recognized as an important mechanism of osteoarthritis (OA), at least in some patients. Among the signs of the inflammatory process are elevated macrophage numbers detected in the OA synovium compared to healthy controls. High macrophage counts also correlate with clinical symptoms of the disease. Macrophages are central players in the development of chronic inflammation, pain, cartilage destruction, and bone remodeling. However, macrophages are also involved in tissue repair and remodeling, including cartilage. Therefore, reduction of macrophage content in the joints correlates with deleterious effects in OA models. Macrophage population is heterogeneous and dynamic, with phenotype transitions being induced by a variety of stimuli. In order to effectively use the macrophage inflammatory circuit for treatment of OA, it is important to understand macrophage heterogeneity and interactions with surrounding cells and tissues in the joint. In this review, we discuss functional phenotypes of macrophages and specific targeting approaches relevant for OA treatment development.
Keywords: inflammation; macrophages; osteoarthritis.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Similar articles
-
Amniotic mesenchymal stem cells mitigate osteoarthritis progression in a synovial macrophage-mediated in vitro explant coculture model.J Tissue Eng Regen Med. 2018 Apr;12(4):1097-1110. doi: 10.1002/term.2610. Epub 2017 Nov 29. J Tissue Eng Regen Med. 2018. PMID: 29131526 Free PMC article.
-
Modulating synovial macrophage pyroptosis and mitophagy interactions to mitigate osteoarthritis progression using functionalized nanoparticles.Acta Biomater. 2024 Jun;181:425-439. doi: 10.1016/j.actbio.2024.05.014. Epub 2024 May 8. Acta Biomater. 2024. PMID: 38729544
-
Targeting STAT6-mediated synovial macrophage activation improves pain in experimental knee osteoarthritis.Arthritis Res Ther. 2024 Mar 20;26(1):73. doi: 10.1186/s13075-024-03309-6. Arthritis Res Ther. 2024. PMID: 38509602 Free PMC article.
-
Emerging Roles of Macrophage Polarization in Osteoarthritis: Mechanisms and Therapeutic Strategies.Orthop Surg. 2024 Mar;16(3):532-550. doi: 10.1111/os.13993. Epub 2024 Jan 31. Orthop Surg. 2024. PMID: 38296798 Free PMC article. Review.
-
Obesity, Inflammation, and Immune System in Osteoarthritis.Front Immunol. 2022 Jul 4;13:907750. doi: 10.3389/fimmu.2022.907750. eCollection 2022. Front Immunol. 2022. PMID: 35860250 Free PMC article. Review.
Cited by
-
Healthy and Osteoarthritis-Affected Joints Facing the Cellular Crosstalk.Int J Mol Sci. 2023 Feb 18;24(4):4120. doi: 10.3390/ijms24044120. Int J Mol Sci. 2023. PMID: 36835530 Free PMC article. Review.
-
Target Role of Monocytes as Key Cells of Innate Immunity in Rheumatoid Arthritis.Diseases. 2024 Apr 25;12(5):81. doi: 10.3390/diseases12050081. Diseases. 2024. PMID: 38785736 Free PMC article. Review.
-
Radical-Generating Activity, Phagocytosis, and Mechanical Properties of Four Phenotypes of Human Macrophages.Int J Mol Sci. 2024 Feb 3;25(3):1860. doi: 10.3390/ijms25031860. Int J Mol Sci. 2024. PMID: 38339139 Free PMC article.
-
The Implications of Brain-Derived Neurotrophic Factor in the Biological Activities of Platelet-Rich Plasma.Inflammation. 2025 Feb;48(1):426-446. doi: 10.1007/s10753-024-02072-9. Epub 2024 Jun 21. Inflammation. 2025. PMID: 38904872
-
M2-like macrophages derived from THP-1 cells promote myofibroblast differentiation of synovial fibroblasts in association with the TGF-β1/SMAD2/3 signaling pathway.Sci Rep. 2025 Jul 15;15(1):25505. doi: 10.1038/s41598-025-10858-6. Sci Rep. 2025. PMID: 40665033 Free PMC article.
References
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical