Huang He, Zhang Zhao-Fei, Qin Feng-Wei, Tang Wang, Liu Dong-Hua, Wu Pei-Yu, Jiao Feng
Department of Orthopedic Surgery, Guangzhou Hospital of Integrated Traditional and Western Medicine, Guangzhou, China.
Mol Genet Genomic Med. 2019 Apr;7(4):e00586. doi: 10.1002/mgg3.586. Epub 2019 Feb 7.
This study focused on the mechanisms where icariin inhibited chondrocyte apoptosis and angiogenesis by regulating the TDP-43 signaling pathway.
A rat osteoarthritis (OA) model was established by collagenase injection. Histological examination of the articular cartilage and synovial tissue was performed 6 weeks after operation. Cartilage cell line overexpressing TDP-43 and mesenchymal stem cell line (TDP43-MSCs) of the rat TDP43 gene were established.
In OA rats transplanted with TDP43-mMSCs, TDP43 was highly expressed in chondrocytes (TDP43-HC), while TDP43 expression was low in HC and MSCs-HC (p < 0.05). After the intervention of MSCs-TDP43, high expression of TDP43 induced the apoptosis and death of chondrocytes. After the addition of icariin, late apoptosis and death of TDP43-HC were significantly attenuated. Apoptosis and death of HC, MSCs-HC, and TDP43-HC cells were effectively controlled with icariin, and no apparent cell death was found. ELISA showed that the VEGF and HIF-1 alpha were significantly higher in the rat OA model than the normal control rats.
TDP43-MSC transplantation interfered with the expression of TDP43 in the articular chondrocytes of OA rats, which may impact on inducing apoptosis of chondrocytes as well as inhibiting the proliferation of chondrocytes. Additionally, TDP43-MSCs appeared to promote the formation of neovascularization in the synovial tissue, which could be significantly attenuated by icariin.
本研究聚焦于淫羊藿苷通过调节TDP - 43信号通路抑制软骨细胞凋亡和血管生成的机制。
通过注射胶原酶建立大鼠骨关节炎(OA)模型。术后6周对关节软骨和滑膜组织进行组织学检查。建立了过表达TDP - 43的软骨细胞系和大鼠TDP43基因的间充质干细胞系(TDP43 - MSCs)。
在移植了TDP43 - mMSCs的OA大鼠中,TDP43在软骨细胞(TDP43 - HC)中高表达,而在HC和MSCs - HC中TDP43表达较低(p < 0.05)。MSCs - TDP43干预后,TDP43的高表达诱导了软骨细胞的凋亡和死亡。加入淫羊藿苷后,TDP43 - HC的晚期凋亡和死亡明显减轻。淫羊藿苷有效控制了HC、MSCs - HC和TDP43 - HC细胞的凋亡和死亡,未发现明显的细胞死亡。ELISA显示,大鼠OA模型中VEGF和HIF - 1α明显高于正常对照大鼠。
TDP43 - MSC移植干扰了OA大鼠关节软骨细胞中TDP43的表达,这可能影响诱导软骨细胞凋亡以及抑制软骨细胞增殖。此外,TDP43 - MSCs似乎促进了滑膜组织中新血管形成,而淫羊藿苷可显著减弱这种作用。