Piovesana Roberta, Faroni Alessandro, Tata Ada Maria, Reid Adam J
Department of Biology and Biotechnologies "Charles Darwin", Sapienza, University of Rome, Rome, Italy.
Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Cell Death Discov. 2025 Apr 13;11(1):170. doi: 10.1038/s41420-025-02404-0.
Human adipose-derived stem cells (ASCs), differentiated in vitro towards Schwann-like phenotype (hdASCs), have been suggested as an alternative source of Schwann cells (SCs). However, although they seem a good alternative, their differentiation is unstable, losing their SC-like phenotype following growth factor withdrawal. Rat and human SCs and rat dASCs have been characterized for acetylcholine M2 muscarinic receptor subtype that plays a strategic role in the regulation of their differentiation. Here, we evaluated the M2 muscarinic receptor activation in controlling hdASC proliferation and stabilization of the hdASC phenotype. In accordance with our data in rats, M2 stimulation results in a reversible decrease of cell growth and migration in hdASCs, negatively modulates proliferation markers and upregulates differentiation markers. Remarkably, hdASC differentiation can be stabilized by M2 receptor activation in the absence of differentiation media maintaining a spindle-shaped morphology and SC-like marker expression. These results show that the M2 receptor enhances the hdASC phenotype, maintaining the expression of key glial markers and supporting their pro-regenerative properties.
人脂肪来源干细胞(ASCs)在体外分化为类雪旺氏细胞表型(hdASCs),已被认为是雪旺氏细胞(SCs)的替代来源。然而,尽管它们似乎是一个很好的替代方案,但其分化不稳定,在生长因子撤除后会失去其类雪旺氏细胞表型。大鼠和人SCs以及大鼠dASCs已被鉴定出具有毒蕈碱型乙酰胆碱M2受体亚型,该亚型在其分化调节中起关键作用。在此,我们评估了M2毒蕈碱受体激活在控制hdASC增殖和稳定hdASC表型方面的作用。根据我们在大鼠中的数据,M2刺激导致hdASCs细胞生长和迁移可逆性降低,负向调节增殖标志物并上调分化标志物。值得注意的是,在没有分化培养基的情况下,M2受体激活可稳定hdASC分化,使其保持纺锤形形态和类雪旺氏细胞标志物表达。这些结果表明,M2受体增强了hdASC表型,维持关键神经胶质标志物的表达并支持其促再生特性。