Department of Biology and Biotechnology Charles Darwin, Sapienza University of Rome, 00185 Rome, Italy.
Department of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome and Policlinico Umberto I, 00185 Rome, Italy.
Biomolecules. 2022 Feb 1;12(2):239. doi: 10.3390/biom12020239.
The cross-talk between axon and glial cells during development and in adulthood is mediated by several molecules. Among them are neurotransmitters and their receptors, which are involved in the control of myelinating and non-myelinating glial cell development and physiology. Our previous studies largely demonstrate the functional expression of cholinergic muscarinic receptors in Schwann cells. In particular, the M2 muscarinic receptor subtype, the most abundant cholinergic receptor expressed in Schwann cells, inhibits cell proliferation downregulating proteins expressed in the immature phenotype and triggers promyelinating differentiation genes. In this study, we analysed the in vitro modulation of the Neuregulin-1 (NRG1)/erbB pathway, mediated by the M2 receptor activation, through the selective agonist arecaidine propargyl ester (APE). M2 agonist treatment significantly downregulates NRG1 and erbB receptors expression, both at transcriptional and protein level, and causes the internalization and intracellular accumulation of the erbB2 receptor. Additionally, starting from our previous results concerning the negative modulation of Notch-active fragment NICD by M2 receptor activation, in this work, we clearly demonstrate that the M2 receptor subtype inhibits erbB2 receptors by Notch-1/NICD downregulation. Our data, together with our previous results, demonstrate the existence of a cross-interaction between the M2 receptor and NRG1/erbB pathway-Notch1 mediated, and that it is responsible for the modulation of Schwann cell proliferation/differentiation.
在发育和成年过程中,轴突和神经胶质细胞之间的串扰是由几种分子介导的。其中包括神经递质及其受体,它们参与调控少突胶质细胞和非少突胶质细胞的发育和生理功能。我们之前的研究很大程度上证明了胆碱能毒蕈碱型受体在施万细胞中的功能性表达。特别是 M2 毒蕈碱型受体亚型,是施万细胞中表达最丰富的胆碱能受体,通过下调幼稚表型中表达的蛋白抑制细胞增殖,并触发促髓鞘分化基因。在这项研究中,我们通过选择性激动剂槟榔碱丙炔酯(APE)分析了 M2 受体激活介导的神经调节蛋白 1(NRG1)/erbB 通路的体外调节。M2 激动剂处理显著下调了 NRG1 和 erbB 受体的表达,包括转录水平和蛋白水平,并导致 erbB2 受体的内化和细胞内积累。此外,基于我们之前关于 M2 受体激活对 Notch 活性片段 NICD 的负调控的研究结果,在这项工作中,我们清楚地证明了 M2 受体亚型通过 Notch-1/NICD 下调抑制 erbB2 受体。我们的数据与之前的结果一起,证明了 M2 受体与 NRG1/erbB 通路之间存在交叉相互作用,并且 Notch1 介导的这种相互作用负责调节施万细胞的增殖/分化。