Phytomedicine : international journal of phytotherapy and phytopharmacology · 2025
Gut microbiota metabolite Urolithin B inhibits chondrocyte ferroptosis by rewriting iron homeostasis via FGFR3/NCOA4/FTH1 axis, alleviating osteoarthritis.
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Li Yanlin, Gu Hanwen, Jiang Xiaotian, Li Jiale, Li Qi, Song Kangle, Kong Xiangzhen, Meng Qunbo, Shi Anhao, Lin Junhao, Chen Bin, Wang Gang, Zhang Hong, Xu Qingjia
Аннотация
BACKGROUND: Osteoarthritis (OA) is a prevalent chronic disease characterized by articular cartilage degeneration. The lack of safe and effective therapies has made OA a leading global cause of disability, severely impacting patient quality of life. Urolithin B (UB), a bioactive metabolite derived from gut microbiota processing of ellagic acid, exhibits potent antioxidant and anti-inflammatory properties, positioning it as a promising therapeutic candidate for OA. However, the precise mechanisms by which UB inhibits OA progression remain unknown.
PURPOSE: This study aimed to evaluate the therapeutic potential of UB for OA and elucidate its underlying mechanisms of action.
METHODS: The therapeutic effects of UB on OA were assessed using interleukin-1β (IL-1β)-induced chondrocyte models and rats subjected to anterior cruciate ligament transection (ACLT). Integrated transcriptome analysis was employed to comprehensively investigate the relevant mechanisms. Fibroblast growth factor receptor 3 (FGFR3)-specific small interfering RNA (siRNA) and overexpression plasmids were utilized in vitro to validate the role of FGFR3 as a specific downstream target of UB and its functional significance in osteoarthritis progression. Furthermore, FGFR3 gene knockdown was performed in UB-treated ACLT rats to confirm the critical role of both UB and its downstream target, FGFR3.
RESULTS: This study reports the novel discovery that UB significantly mitigates IL-1β-induced extracellular matrix degradation and alleviates OA progression through a previously unrecognized mechanism involving iron homeostasis regulation. Mechanistically, we demonstrate that UB inhibits chondrocyte ferroptosis by upregulating FGFR3 expression, which suppresses ferritinophagy by disrupting the interaction between nuclear receptor coactivator 4 (NCOA4) and ferritin heavy chain 1 (FTH1). Our findings establish the novel protective role of the FGFR3/NCOA4/FTH1 signaling axis in chondrocytes under inflammatory conditions by restoring iron homeostasis.
CONCLUSIONS: We identified FGFR3 as a novel therapeutic target for the prevention and alleviation of OA. The validation of UB as a functional agonist of FGFR3, revealing its potential as a new therapeutic candidate and providing a new perspective for combating OA.
PURPOSE: This study aimed to evaluate the therapeutic potential of UB for OA and elucidate its underlying mechanisms of action.
METHODS: The therapeutic effects of UB on OA were assessed using interleukin-1β (IL-1β)-induced chondrocyte models and rats subjected to anterior cruciate ligament transection (ACLT). Integrated transcriptome analysis was employed to comprehensively investigate the relevant mechanisms. Fibroblast growth factor receptor 3 (FGFR3)-specific small interfering RNA (siRNA) and overexpression plasmids were utilized in vitro to validate the role of FGFR3 as a specific downstream target of UB and its functional significance in osteoarthritis progression. Furthermore, FGFR3 gene knockdown was performed in UB-treated ACLT rats to confirm the critical role of both UB and its downstream target, FGFR3.
RESULTS: This study reports the novel discovery that UB significantly mitigates IL-1β-induced extracellular matrix degradation and alleviates OA progression through a previously unrecognized mechanism involving iron homeostasis regulation. Mechanistically, we demonstrate that UB inhibits chondrocyte ferroptosis by upregulating FGFR3 expression, which suppresses ferritinophagy by disrupting the interaction between nuclear receptor coactivator 4 (NCOA4) and ferritin heavy chain 1 (FTH1). Our findings establish the novel protective role of the FGFR3/NCOA4/FTH1 signaling axis in chondrocytes under inflammatory conditions by restoring iron homeostasis.
CONCLUSIONS: We identified FGFR3 as a novel therapeutic target for the prevention and alleviation of OA. The validation of UB as a functional agonist of FGFR3, revealing its potential as a new therapeutic candidate and providing a new perspective for combating OA.