藤黄蛋白C
细胞生物学
细胞迁移
整合素
蛋白激酶B
干细胞
焦点粘着
基因敲除
信号转导
PI3K/AKT/mTOR通路
再生(生物学)
小干扰RNA
化学
生物
细胞
核糖核酸
细胞外基质
基因
生物化学
作者
Kang Xu,Yibo Shao,Yi Xia,Yuna Qian,Nan Jiang,Xianqiong Liu,Li Yang,Chunli Wang
出处
期刊:Biofactors
[Wiley]
日期:2021-05-31
卷期号:47 (5): 768-777
被引量:22
摘要
Insufficient attention has been focused on the directional migration of SOX10+ tendon stem cells (STSCs) during tendon remodeling. Here, we investigate whether tenascin-C (TNC) promotes STSC motility and migration. Based on the hypothesis that TNCs induce STSC migration, RNA-sequencing (RNA-seq) was conducted, identifying 2107 differentially expressed genes (DEGs), of which 1272 were up-regulated and 835 down-regulated following treatment with TNC versus the control. The DEGs were principally involved in cell adhesion and cell membrane signal transduction. Highly enriched-related signaling included the PI3K-Akt, focal adhesion, and ECM-receptor interaction pathways. Protein interaction analysis established that TNC was positively correlated with ITGA9 (integrin-α9). Furthermore, TNC activated the phosphorylation levels of FAK and Akt, and knockdown of ITGA9 with siRNA revealed that TNC contributes to STSC migration via the targeting of ITGA9. In addition, in vivo administration of TNC promoted tissue regeneration of injured tendons. In conclusion, TNC regulated the migration of STSCs via ITGA9, thereby promoting the regeneration of tendon injuries.
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