Irisin promotes the proliferation and tenogenic differentiation of rat tendon-derived stem/progenitor cells via activating YAP/TAZ

被引:6
|
作者
Xu, Langhai [1 ]
Chen, Zhonggai [2 ,3 ]
Geng, Tingting [4 ]
Ru, Bin [1 ]
Wan, Quan [1 ]
Zhang, Jianbin [5 ]
Li, Shun [1 ]
Cai, Wenjun [1 ]
机构
[1] Hangzhou Med Coll, Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Pain, Hangzhou, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 2, Dept Orthopaed, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[4] Zhejiang Shuren Univ, Shulan Int Med Coll, Shulan Hangzhou Hosp, Hangzhou, Peoples R China
[5] Hangzhou Med Coll, Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Oncol,Clin Res Inst, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell differentiation; Irisin; Stem cells; Tissue engineering; YAP; TAZ; HIPPO SIGNALING PATHWAY; STEM-CELLS; GROWTH-FACTORS; BONE; REGENERATION; EXPRESSION; MATRIX; REPAIR;
D O I
10.1007/s11626-022-00699-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tendinopathy is a common tendon disorder characterized by pain, swelling, and dysfunction. Current evidence has demonstrated that the depletion of stem cell pool and non-tenogenic differentiation of tendon-derived stem/progenitor cells (TSPCs) might account for the pathogenesis of tendinopathy. FNDC5/Irisin, as a novel exercise-induced myokine, is proved to be involved in the exercise-induced protective effects on musculoskeletal disorders. However, whether irisin can affect TSPCs fate is still unknown. To ascertain the roles of irisin on the proliferation and tenogenic differentiation of TSPCs, rat TSPCs were isolated and incubated with irisin. Cell viability, phenotypic changes, and related signaling pathways were evaluated by CCK-8 assay, colony formation assay, real-time PCR, Western blot, immunofluorescence, and proteasome activity assay. We found that irisin treatment increased the proliferative and colony-forming abilities, and promoted the tenogenic differentiation of TSPCs by upregulating the expression of YAP/TAZ. In conclusion, our work showed for the first time that irisin promotes the proliferation and tenogenic differentiation of rat TSPCs in vitro by activating YAP/TAZ, and the process was associated with a ubiquitin-proteasome proteolytic pathway. In conclusion, irisin and agents targeting YAP/TAZ may be promising therapeutic options for tendinopathy.
引用
收藏
页码:658 / 668
页数:11
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