Yu Yang, Zhou Yulong, Cheng Tao, Lu Xiaolang, Yu Kehe, Zhou Yifei, Hong Jianjun, Chen Ying
Department of Orthopaedics, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325000, China.
Emergency Department, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325000, China.
Cell Prolif. 2016 Apr;49(2):173-84. doi: 10.1111/cpr.12250. Epub 2016 Mar 29.
Tissue engineering is a promising approach for repair of tendon injuries. Adipose-derived mesenchymal stem cells (ADMSCs) have gained increasing research interest for their potential in improving healing and regeneration of injured tendons. The present study aimed to investigate effects of O2 tension and potential signalling pathways on AMDSC differentiation into tenocytes, in an indirect co-culture system.
Human ADMSCs were co-cultured under normoxia (20% O2 ) and also under hypoxia (2% O2 ). Tenocyte differentiation of AMDSCs and expression of hypoxia-inducible factor-1 (HIF-1α) were analysed by reverse transcription-PCR, Western blotting and immunohistochemistry. Furthermore, HIF-1α inhibitor and inducer (FG-4592) effects on differentiation of AMDSCs were studied using qPCR, immunofluorescence and Western blotting.
Indirect co-culture with tenocytes increased differentiation of ADMSCs into tenocytes; furthermore, hypoxia further enhanced tenocyte differentiation of AMDSCs, accompanied by increased expression of HIF-1α. HIF-1α inhibitor attenuated effects of hypoxia on differentiation of ADMSCs; in contrast, FG-4592 increased differentiation of ADMSCs under both hypoxia and normoxia.
Taken together, we found that growing ADMSCs under hypoxia, or activating expression of HIF-1α to be important in differentiation of ADMSCs, which provides a foundation for application of ADMSCs in vivo for tendon regeneration.
组织工程是修复肌腱损伤的一种有前景的方法。脂肪来源的间充质干细胞(ADMSCs)因其在促进损伤肌腱愈合和再生方面的潜力而受到越来越多的研究关注。本研究旨在探讨在间接共培养系统中,氧张力和潜在信号通路对ADMSCs向肌腱细胞分化的影响。
人ADMSCs在常氧(20% O₂)和低氧(2% O₂)条件下进行共培养。通过逆转录聚合酶链反应、蛋白质免疫印迹法和免疫组织化学分析ADMSCs的肌腱细胞分化及缺氧诱导因子-1(HIF-1α)的表达。此外,使用实时定量聚合酶链反应、免疫荧光和蛋白质免疫印迹法研究HIF-1α抑制剂和诱导剂(FG-4592)对ADMSCs分化的影响。
与肌腱细胞间接共培养增加了ADMSCs向肌腱细胞的分化;此外,低氧进一步增强了ADMSCs的肌腱细胞分化,同时伴有HIF-1α表达增加。HIF-1α抑制剂减弱了低氧对ADMSCs分化的影响;相反,FG-4592在低氧和常氧条件下均增加了ADMSCs的分化。
综上所述,我们发现低氧条件下培养ADMSCs或激活HIF-1α的表达对ADMSCs的分化很重要,这为ADMSCs在体内用于肌腱再生的应用提供了基础。