Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling

被引:31
|
作者
Wang, Yunjiao [1 ]
He, Gang [1 ]
Wang, Feng [1 ]
Zhang, Chenke [1 ]
Ge, Zilu [1 ]
Zheng, Xiaolong [1 ]
Deng, Honghao [1 ]
Yuan, Chengsong [1 ]
Zhou, Binghua [1 ]
Tao, Xu [1 ]
Zhang, Jiqiang [2 ]
Tang, Kanglai [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Orthopaed, State Key Lab Trauma Burn & Combined Injury,Sport, Gaotanyan St 30, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Dept Neurol, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
adipogenesis; aspirin; tendinopathy; tendon stem cells; STABLE ANALOGS; ANIMAL-MODELS; RESPONSES; SAFETY; REPAIR; WINDOW; A(4);
D O I
10.1111/jcmm.14622
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tendon injury repairs are big challenges in sports medicine, and fatty infiltration after tendon injury is very common and hampers tendon injury healing process. Tendon stem cells (TSCs), as precursors of tendon cells, have shown promising effect on injury tendon repair for their tenogenesis and tendon extracellular matrix formation. Adipocytes and lipids accumulation is a landmark event in pathological process of tendon injury, and this may induce tendon rupture in clinical practice. Based on this, it is important to inhibit TSCs adipogenesis and lipids infiltration to restore structure and function of injury tendon. Aspirin, as the representative of non-steroidal anti-inflammatory drugs (NSAIDs), has been widely used in tendon injury for its anti-inflammatory and analgesic actions, but effect of aspirin on TSCs adipogenesis and fatty infiltration is still unclear. Under adipogenesis conditions, TSCs were treated with concentration gradient of aspirin. Oil red O staining was performed to observe changes of lipids accumulation. Next, we used RNA sequencing to compare profile changes of gene expression between induction group and aspirin-treated group. Then, we verified the effect of filtrated signalling on TSCs adipogenesis. At last, we established rat tendon injury model and compared changes of biomechanical properties after aspirin treatment. The results showed that aspirin decreased lipids accumulation in injury tendon and inhibited TSCs adipogenesis. RNA sequencing filtrated PTEN/PI3K/AKT signalling as our target. After adding the signalling activators of VO-Ohpic and IGF-1, inhibited adipogenesis of TSCs was reversed. Still, aspirin promoted maximum loading, ultimate stress and breaking elongation of injury tendon. In conclusion, by down-regulating PTEN/PI3K/AKT signalling, aspirin inhibited adipogenesis of TSCs and fatty infiltration in injury tendon, promoted biomechanical properties and decreased rupture risk of injury tendon. All these provided new therapeutic potential and medicine evidence of aspirin in treating tendon injury and tendinopathy.
引用
收藏
页码:7535 / 7544
页数:10
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