The C5AR1/TNFSF13B axis alleviates osteoarthritis by activating the PI3K/Akt/GSK3β/Nrf2/HO-1 pathway to inhibit ferroptosis

• Published in: Experimental cell research Vol. 441; no. 2; p. 114195
• Main Authors: Lv, Min, Cai, Yuanzhen, Hou, Weikun, Peng, Kan, Xu, Ke, Lu, Chao, Yu, Wenxing, Zhang, Weisong, Liu, Lin
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.08.2024
• Subjects: Animals; C5AR1; Chondrocytes - drug effects; Chondrocytes - metabolism; Chondrocytes - pathology; Ferroptosis; Ferroptosis - drug effects; Glycogen Synthase Kinase 3 beta - genetics; Glycogen Synthase Kinase 3 beta - metabolism; Heme Oxygenase (Decyclizing); Heme Oxygenase-1 - genetics; Heme Oxygenase-1 - metabolism; Male; NF-E2-Related Factor 2 - genetics; NF-E2-Related Factor 2 - metabolism; Osteoarthritis; Osteoarthritis - genetics; Osteoarthritis - metabolism; Osteoarthritis - pathology; Phosphatidylinositol 3-Kinases - metabolism; PI3K/Akt/GSK3β/Nrf2/HO-1 pathway; Proto-Oncogene Proteins c-akt - metabolism; Rats; Rats, Sprague-Dawley; Receptor, Anaphylatoxin C5a - genetics; Receptor, Anaphylatoxin C5a - metabolism; Signal Transduction; TNFSF13B; Ferroptosis; PI3K/Akt/GSK3β/Nrf2/HO-1 pathway; Osteoarthritis; C5AR1; TNFSF13B
• ISSN: 0014-4827; 1090-2422; 1090-2422
• DOI: 10.1016/j.yexcr.2024.114195

Chondrocyte ferroptosis induces the occurrence of osteoarthritis (OA). As a key gene of OA, C5a receptor 1 (C5AR1) is related to ferroptosis. Here, we investigated whether C5AR1 interferes with chondrocyte ferroptosis during OA occurrence. C5AR1 was downregulated in PA-treated chondrocytes. Overexpression of C5AR1 increased the cell viability and decreased ferroptosis in chondrocytes. Moreover, Tumor necrosis factor superfamily member 13B (TNFSF13B) was downregulated in PA-treated chondrocytes, and knockdown of TNFSF13B eliminated the inhibitory effect of C5AR1 on ferroptosis in chondrocytes. More importantly, the PI3K/Akt/GSK3β/Nrf2/HO-1 pathway inhibitor LY294002 reversed the inhibition of C5AR1 or TNFSF13B on ferroptosis in chondrocytes. Finally, we found that C5AR1 alleviated joint tissue lesions and ferroptosis in rats and inhibited the progression of OA in the rat OA model constructed by anterior cruciate ligament transection (ACLT), which was reversed by interfering with TNFSF13B. This study shows that C5AR1 reduces the progression of OA by upregulating TNFSF13B to activate the PI3K/Akt/GSK3β/Nrf2/HO-1 pathway and thereby inhibiting chondrocyte sensitivity to ferroptosis, indicating that C5AR1 may be a potential therapeutic target for ferroptosis-related diseases.