Department of Burns and Plastic Surgery, Affiliated Hospital of Zunyi Medical College, 149 Dalian Road, Guizhou, Zunyi, China.
Cell Tissue Res. 2021 Apr;384(1):99-112. doi: 10.1007/s00441-020-03320-8. Epub 2021 Jan 15.
Human amniotic mesenchymal stem cells (hAMSCs) can be differentiated into Schwann-cell-like cells (SCLCs) in vitro. However, the underlying mechanism of cell differentiation remains unclear. In this study, we explored the phenotype and multipotency of hAMSCs, which were differentiated into SCLCs, and the expression of nerve repair-related Schwann markers, such as S100 calcium binding protein B (S-100), TNF receptor superfamily member 1B (P75), and glial fibrillary acidic protein (GFAP) were observed to be significantly increased. The secreted functional neurotrophic factors, like brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), and neurotrophin-3 (NT-3), were determined and also increased with the differentiation time. Moreover, miR-146a-3p, which significantly decreased during the differentiation of hAMSCs into SCLCs, was selected by miRNA-sequence analysis. Further molecular mechanism studies showed that Erb-B2 receptor tyrosine kinase 2 (ERBB2) was an effective target of miR-146a-3p and that miR-146a-3p down-regulated ERBB2 expression by binding to the 3'-UTR of ERBB2. The expression of miR-146a-3p markedly decreased, while the mRNA levels of ERBB2 increased with the differentiation time. The results showed that down-regulating miR-146a-3p could promote SC lineage differentiation and suggested that miR-146a-3p negatively regulated the Schwann-like phenotype differentiation of hAMSCs by targeting ERBB2. The results will be helpful to establish a deeper understanding of the underlying mechanisms and find novel strategies for cell therapy.
人羊膜间充质干细胞(hAMSCs)在体外可分化为施万细胞样细胞(SCLCs)。然而,细胞分化的潜在机制尚不清楚。在这项研究中,我们探索了 hAMSCs 向 SCLCs 分化后的表型和多能性,观察到神经修复相关的施万细胞标志物如 S100 钙结合蛋白 B(S-100)、肿瘤坏死因子受体超家族成员 1B(P75)和神经胶质纤维酸性蛋白(GFAP)的表达显著增加。分泌的功能性神经营养因子,如脑源性神经营养因子(BDNF)、神经生长因子(NGF)和神经营养素-3(NT-3)也被测定并随着分化时间的增加而增加。此外,miRNA 测序分析发现,hAMSCs 向 SCLCs 分化过程中显著下调的 miR-146a-3p 被选中。进一步的分子机制研究表明,表皮生长因子受体酪氨酸激酶 2(ERBB2)是 miR-146a-3p 的有效靶点,miR-146a-3p 通过结合 ERBB2 的 3'-UTR 下调 ERBB2 的表达。miR-146a-3p 的表达显著降低,而 ERBB2 的 mRNA 水平随分化时间增加而增加。结果表明,下调 miR-146a-3p 可以促进 SC 谱系分化,并表明 miR-146a-3p 通过靶向 ERBB2 负调控 hAMSCs 的施万样表型分化。这些结果将有助于更深入地了解潜在机制,并为细胞治疗找到新的策略。