Potential involvement of connective tissue growth factor in chondrocytes apoptosis of Kashin-Beck disease

Kashin-Beck disease (KBD) is an endemic osteoarthropathy characterized by excessive chondrocytes apoptosis. T-2 toxin exposure has been proved to be its etiology. Connective tissue growth factor (CTGF) exerts a profound influence on cartilage growth and metabolism. We investigated the potential role...

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Veröffentlicht in:Ecotoxicology and environmental safety 2024-10, Vol.285, p.117148, Article 117148
Hauptverfasser: Yang, Xuena, Liu, Huan, Cheng, Shiqiang, Pan, Chuyu, Cai, Qingqing, Chu, Xiaoge, Shi, Sirong, Wei, Wenming, He, Dan, Cheng, Bolun, Wen, Yan, Jia, Yumeng, Tinkov, Alexey A., Skalny, Anatoly V., Zhang, Feng
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Sprache:eng
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Zusammenfassung:Kashin-Beck disease (KBD) is an endemic osteoarthropathy characterized by excessive chondrocytes apoptosis. T-2 toxin exposure has been proved to be its etiology. Connective tissue growth factor (CTGF) exerts a profound influence on cartilage growth and metabolism. We investigated the potential role of CTGF in KBD development and examined CTGF alterations under T-2 toxin stimulation. The levels of CTGF and chondrocyte apoptosis-related markers in cartilage and primary chondrocytes from KBD and control groups were measured using qRT-PCR, Western blotting, immunohistochemistry, and immunofluorescence. We analyzed expression changes of these genes in response to T-2 toxin. Apoptosis rates of chondrocytes induced by T-2 toxin were measured by flow cytometry and TUNEL assay. The active pharmaceutical ingredient targeting CTGF was screened through Comparative Toxicogenomics Database, and molecular docking was performed using AutoDock Tools. The CTGF levels in KBD cartilage and chondrocytes were significantly elevated and positively associated with the levels of apoptosis-related genes. T-2 toxin exposure increased CTGF and apoptosis-related gene levels in chondrocytes, with apoptosis rates rising alongside T-2 toxin concentration. Curcumin was identified as targeting CTGF and exhibited effective binding. It could down-regulate CTGF, apoptosis-related genes, such as Cleaved caspase 3 and BAX, and also significantly reduce apoptosis rate in chondrocytes treated with T-2 toxin. CTGF plays a crucial role in the development of KBD. Curcumin has shown potential in inhibiting CTGF levels and reducing chondrocyte apoptosis, highlighting its promise as a therapeutic agent for preventing cartilage damage in KBD. Our findings provided valuable insights into the pathogenesis of KBD and could promote the development of novel therapeutic strategies for this debilitating disease. •The levels of CTGF were increased in cartilage and chondrocytes of KBD, and positively associated with apoptosis levels.•T-2 toxin can up-regulate the expression levels of CTGF and induce the apoptosis in the chondrocytes.•Curcumin could down-regulate CTGF expression and attenuate the apoptosis rate of chondrocytes treated with T-2 toxin.
ISSN:0147-6513
1090-2414
1090-2414
DOI:10.1016/j.ecoenv.2024.117148