Marine Science Institute, The University of Texas at Austin, 750 Channel View Drive, Port Aransas (TX), 78373, United States.
Marine Science Institute, The University of Texas at Austin, 750 Channel View Drive, Port Aransas (TX), 78373, United States.
Mol Cell Endocrinol. 2021 Jul 1;531:111298. doi: 10.1016/j.mce.2021.111298. Epub 2021 Apr 27.
Membrane progesterone receptors (mPRs) were recently found to be present and active in Schwann cells, where they have a potentially pro-regenerative activity. In this study, we investigated the role of mPRs in human adipose stem cells (ASC) differentiated into Schwann cell-like cells (SCL-ASC), which represent a promising alternative to Schwann cells for peripheral nerve regeneration. Our findings show that mPRs are present both in undifferentiated and differentiated ASC, and that the differentiation protocol upregulates mPR expression. Activation of mPRα promoted cell migration and differentiation in SCL-ASC, alongside with changes in cell morphology and mPRα localization. Moreover, it increased the expression and release of BDNF, a neurotrophin with pro-regenerative activity. Further analysis showed that Src and PI3K-Akt signaling pathways are involved in mPRα activity in SCL-ASC. These findings suggest that mPRα could play a pro-regenerative role in SCL-ASC and may be a promising target for the promotion of peripheral nerve regeneration.
膜孕激素受体(mPRs)最近被发现在雪旺细胞中存在并具有活性,在那里它们具有潜在的促再生活性。在这项研究中,我们研究了 mPRs 在人类脂肪干细胞(ASC)分化为雪旺细胞样细胞(SCL-ASC)中的作用,SCL-ASC 是外周神经再生的雪旺细胞有前途的替代品。我们的研究结果表明,mPRs 存在于未分化和分化的 ASC 中,分化方案上调了 mPR 的表达。mPRα 的激活促进了 SCL-ASC 中的细胞迁移和分化,同时改变了细胞形态和 mPRα 的定位。此外,它增加了神经营养因子 BDNF 的表达和释放,BDNF 具有促再生活性。进一步的分析表明,Src 和 PI3K-Akt 信号通路参与了 SCL-ASC 中 mPRα 的活性。这些发现表明 mPRα 可能在外周神经再生中发挥促再生作用,可能是促进外周神经再生的有前途的靶点。