Institute of Cellular and Systems Medicine, National Health Research Institutes, 35 Keyan Road, Zhunan Town, Miaoli County, 35053, Taiwan, R.O.C.
Institute of Cellular and Systems Medicine, National Health Research Institutes, 35 Keyan Road, Zhunan Town, Miaoli County, 35053, Taiwan, R.O.C..
Sci Rep. 2017 Jul 10;7(1):4946. doi: 10.1038/s41598-017-05131-4.
Brain neural stem cells and transit amplifying cells in the subventricular zone (SVZ) of the lateral ventricles are in direct contact with the microvascular endothelium. The mechanisms/molecules of direct cell contact in the SVZ neurovascular niche are not fully understood. We previously showed that neural stem/progenitor (NS/P) cells induce brain endothelial signaling in direct cell contact through matriptase (MTP) on NS/P cell surface. In the present study, using pull-down and LC-MS/MS, we identified melanoma cell adhesion molecule (MCAM) the brain endothelial molecule that interacts with MTP. MCAM physically binds to the CUB domains of MTP and induces a chain of brain endothelial signaling including p38MAPK activation, GSK3β inactivation and subsequently β-catenin activation; none of these signaling events occurred when either MTP or MCAM is deleted. MTP-MCAM binding and induction of endothelial signaling were all sensitive to cholera toxin. Together, we identified key molecules that may represent a mechanism in neural stem cell vascular niche regulation.
脑室下区(SVZ)的脑神经干细胞和过渡扩增细胞与微血管内皮直接接触。SVZ 神经血管壁龛中直接细胞接触的机制/分子尚未完全阐明。我们之前的研究表明,神经干细胞/祖细胞(NS/P)细胞通过 NS/P 细胞表面的组织蛋白酶(MTP)在直接细胞接触中诱导脑内皮信号。在本研究中,我们使用下拉和 LC-MS/MS 鉴定了黑色素瘤细胞黏附分子(MCAM),该分子与 MTP 相互作用。MCAM 与 MTP 的 CUB 结构域物理结合,并诱导一系列脑内皮信号,包括 p38MAPK 激活、GSK3β失活,随后β-连环蛋白激活;当 MTP 或 MCAM 缺失时,这些信号事件都不会发生。MTP-MCAM 结合和内皮信号诱导均对霍乱毒素敏感。综上所述,我们鉴定了可能代表神经干细胞血管壁龛调节机制的关键分子。