Clinical College, Ningxia Medical University, Yinchuan, China; Orthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, China.
Clinical College, Ningxia Medical University, Yinchuan, China.
Biomol Biomed. 2023 Feb 1;23(1):77-88. doi: 10.17305/bjbms.2022.7677.
Osteoarthritis (OA) is an age-related degenerative disease characterized by cartilage degeneration and abnormal bone remodeling in the subchondral bone. Autophagy maintains cellular homeostasis by self-phagocytosis. However, the underlying mechanisms of autophagy on the pathological progression of OA are still unknown. This study assessed the effects of autophagy on cartilage and subchondral bone in a mouse OA model. A mouse OA model was induced using destabilization of the medial meniscus (DMM) surgery. Assessment was performed by histomorphology, microcomputed tomography (micro-CT), immunohistochemical, immunofluorescent, and tartrate-resistant acid phosphatase (TRAP) staining. Our data revealed that autophagy can significantly delay the pathological progression of OA by increasing the thickness of hyaline cartilage and decreasing the thickness of calcified cartilage, increasing the subchondral bone volume fraction and bone mineralization density, and decreasing trabecular separation in the early stages of OA (2 weeks), whereas the opposite is true in the late stages of OA (8 weeks). Mechanistically, activation of autophagy in cartilage increased the expression of type II collagen (Col II), decreased the expression of matrix metalloproteinase 13 (MMP 13) and decreased the pyroptosis mediated by NOD-like receptor protein 3 (NLRP3) inflammasome by decreasing the expression of NLRP3, caspase-1, gasdermin D (GSDMD), and IL-1β. In the subchondral bone, activation of autophagy decreased the generation of mature osteoclasts at the early stages of OA (2 weeks) mainly by reducing the receptor activator for nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) ratio, while it decreased osteoblastogenesis by reducing Runt-related transcription factor 2 (Runx2) expression significantly in the late stages of OA (8 weeks). In conclusion, autophagy may delay the pathological progression of OA in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling.
骨关节炎(OA)是一种与年龄相关的退行性疾病,其特征为软骨退变和软骨下骨的异常骨重塑。自噬通过自噬来维持细胞内稳态。然而,自噬对 OA 病理进展的潜在机制尚不清楚。本研究评估了自噬对 OA 小鼠模型中软骨和软骨下骨的影响。使用内侧半月板不稳定(DMM)手术诱导 OA 小鼠模型。通过组织形态学、微计算机断层扫描(micro-CT)、免疫组织化学、免疫荧光和抗酒石酸酸性磷酸酶(TRAP)染色进行评估。我们的数据表明,自噬可以通过增加透明软骨的厚度和减少钙化软骨的厚度、增加软骨下骨体积分数和骨矿化密度以及减少 OA 早期(2 周)的小梁分离来显著延迟 OA 的病理进展,而在 OA 晚期(8 周)则相反。在机制上,软骨中自噬的激活通过增加 II 型胶原(Col II)的表达、减少基质金属蛋白酶 13(MMP 13)的表达和减少 NOD 样受体蛋白 3(NLRP3)炎性体介导的细胞焦亡来减少 NLRP3、半胱天冬酶-1、Gasdermin D(GSDMD)和 IL-1β的表达,从而增加软骨的表达。在软骨下骨中,自噬的激活在 OA 早期(2 周)主要通过降低核因子-κB 受体激活剂配体(RANKL)/骨保护素(OPG)的比值来减少成熟破骨细胞的生成,而在 OA 晚期(8 周)则通过显著降低 Runt 相关转录因子 2(Runx2)的表达来减少成骨细胞的生成。总之,自噬可能通过抑制软骨细胞细胞焦亡和改善软骨下骨重塑来延迟 OA 病理进展。