Department of Biomedical Sciences, Chonnam National University Medical School, Hwasun 58128, Korea.
Department of Orthopaedics Surgery, Center for Joint Disease of Chonnam National University Hwasun Hospital, 322 Seoyang-ro, Hwasun-eup 519-763, Korea.
Int J Mol Sci. 2022 Oct 27;23(21):13016. doi: 10.3390/ijms232113016.
Osteoarthritis (OA) is a low-grade inflammatory disorder of the joints that causes deterioration of the cartilage, bone remodeling, formation of osteophytes, meniscal damage, and synovial inflammation (synovitis). The synovium is the primary site of inflammation in OA and is frequently characterized by hyperplasia of the synovial lining and infiltration of inflammatory cells, primarily macrophages. Macrophages play a crucial role in the early inflammatory response through the production of several inflammatory cytokines, chemokines, growth factors, and proteinases. These pro-inflammatory mediators are activators of numerous signaling pathways that trigger other cytokines to further recruit more macrophages to the joint, ultimately leading to pain and disease progression. Very few therapeutic alternatives are available for treating inflammation in OA due to the condition's low self-healing capacity and the lack of clear diagnostic biomarkers. In this review, we opted to explore the immunomodulatory properties of mesenchymal stem cells (MSCs) and their paracrine mediators-dependent as a therapeutic intervention for OA, with a primary focus on the practicality of polarizing macrophages as suppression of M1 macrophages and enhancement of M2 macrophages can significantly reduce OA symptoms.
骨关节炎(OA)是一种低水平炎症性关节疾病,可导致软骨恶化、骨重塑、骨赘形成、半月板损伤和滑膜炎症(滑膜炎)。滑膜是 OA 中炎症的主要部位,通常表现为滑膜衬里增生和炎症细胞浸润,主要是巨噬细胞。巨噬细胞通过产生几种炎症细胞因子、趋化因子、生长因子和蛋白酶,在早期炎症反应中发挥关键作用。这些促炎介质是许多信号通路的激活剂,这些通路会进一步招募更多的巨噬细胞进入关节,最终导致疼痛和疾病进展。由于 OA 的自我修复能力低,缺乏明确的诊断生物标志物,因此治疗 OA 炎症的治疗方法非常有限。在这篇综述中,我们选择探讨间充质干细胞(MSCs)的免疫调节特性及其旁分泌介质作为 OA 的治疗干预措施,主要关注极化巨噬细胞作为抑制 M1 巨噬细胞和增强 M2 巨噬细胞的实用性,因为这可以显著减轻 OA 症状。