Cai Weixia, Liu Yang, Zhang Ting, Ji Peng, Tian Chenyang, Liu Jiaqi, Zheng Zhao
Department of Burns and Cutaneous Surgery, Xijing Hospital, Fourth Military Medical University, 127 Changle West Road, Xi'an, Shaanxi, 710032, China.
Department of Burns and Cutaneous Surgery, Xijing Hospital, Fourth Military Medical University, 127 Changle West Road, Xi'an, Shaanxi, 710032, China.
Arch Biochem Biophys. 2024 Mar;753:109893. doi: 10.1016/j.abb.2024.109893. Epub 2024 Feb 1.
Adipose tissue-derived stem cells (ADSCs) are a kind of stem cells with multi-directional differentiation potential, which mainly restore tissue repair function and promote cell regeneration. It can be directionally differentiated into Schwann-like cells to promote the repair of peripheral nerve injury. Glial cell line-derived neurotrophic factor (GDNF) plays an important role in the repair of nerve injury, but the underlying mechanism remains unclear, which seriously limits its further application.The study aimed to identify the molecular mechanism by which overexpression of glial cell line-derived neurotrophic factor (GDNF) facilitates the differentiation of ADSCs into Schwann cells, enhancing nerve regeneration after injury. In vitro, ADSCs overexpressing GDNF for 48 h exhibited changes in their morphology, with 80% of the cells having two or more prominences. Compared with that of ADSCs, GDNF-ADSCs exhibited increased expression of the Schwann cell marker S100, nerve damage repair-related factors.ADSC cells in normal culture and ADSC cells were overexpressing GDNF(GDNF-ADSCs) were analysed using TMT-Based Proteomic Analysis and revealed a significantly higher expression of MTA1 in GDNF-ADSCs than in control ADSCs. Hes1 expression was significantly higher in GDNF-ADSCs than in ADSCs and decreased by MTA1 silencing, along with a simultaneous decrease in the expression of S100 and nerve damage repair factors. These findings indicate that GDNF promotes the differentiation of ADSCs into Schwann cells and induces factors that accelerate peripheral nerve damage repair.
脂肪组织来源的干细胞(ADSCs)是一种具有多向分化潜能的干细胞,主要恢复组织修复功能并促进细胞再生。它可以定向分化为类雪旺细胞,以促进周围神经损伤的修复。胶质细胞源性神经营养因子(GDNF)在神经损伤修复中起重要作用,但其潜在机制仍不清楚,这严重限制了其进一步应用。本研究旨在确定胶质细胞源性神经营养因子(GDNF)过表达促进ADSCs向雪旺细胞分化、增强损伤后神经再生的分子机制。在体外,过表达GDNF 48小时的ADSCs形态发生变化,80%的细胞有两个或更多的突起。与ADSCs相比,GDNF-ADSCs中雪旺细胞标志物S100、神经损伤修复相关因子的表达增加。使用基于TMT的蛋白质组学分析对正常培养的ADSC细胞和过表达GDNF的ADSC细胞(GDNF-ADSCs)进行分析,结果显示GDNF-ADSCs中MTA1的表达明显高于对照ADSCs。GDNF-ADSCs中Hes1的表达明显高于ADSCs,并且通过MTA1沉默而降低,同时S100和神经损伤修复因子的表达也降低。这些发现表明,GDNF促进ADSCs向雪旺细胞分化,并诱导加速周围神经损伤修复的因子。