Tenascin‐C regulates migration of SOX10 tendon stem cells via integrin‐α9 for promoting patellar tendon remodeling

• Published in: BioFactors (Oxford) Vol. 47; no. 5; pp. 768 - 777
• Main Authors: Xu, Kang, Shao, Yibo, Xia, Yi, Qian, Yuna, Jiang, Nan, Liu, Xianqiong, Yang, Li, Wang, Chunli
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.09.2021
• Subjects: Animals; Cell Adhesion - genetics; cell motility; Cell Proliferation - genetics; Disease Models, Animal; integrin; Integrin alpha Chains - genetics; Integrin alpha Chains - metabolism; Patellar Ligament - injuries; Patellar Ligament - metabolism; Rats; Rats, Sprague-Dawley; Signal Transduction - genetics; SOXE Transcription Factors - genetics; SOXE Transcription Factors - metabolism; stem cells; Stem Cells - metabolism; Tenascin - genetics; Tenascin - metabolism; tendon regeneration; Transwell; Up-Regulation - genetics; cell motility; stem cells; integrin; tendon regeneration; Transwell
• ISSN: 0951-6433; 1872-8081
• DOI: 10.1002/biof.1759

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.