Department of Biological Sciences, Hunter College, City University of New York, NY, USA.
Icahn Medical Institute 12-52, Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, New York, NY, USA.
FEBS Lett. 2020 May;594(9):1389-1402. doi: 10.1002/1873-3468.13740. Epub 2020 Feb 6.
Rap1 is a small GTPase that has been implicated in dendritic development and plasticity. In this study, we investigated the role of Rap1 in axonal growth and its activation in response to neurotrophins and myelin-associated inhibitors. We report that Rap1 is activated by brain-derived neurotrophic factor and that this activation can be blocked by myelin-associated glycoprotein (MAG) or central nervous system myelin, which also induced increases in Rap1GAP1 levels. In addition, we demonstrate that adenoviral overexpression of Rap1 enhances neurite outgrowth in the presence of MAG and myelin, while inhibition of Rap1 activity through overexpression of Rap1GAP1 blocks neurite outgrowth. These findings suggest that Rap1GAP1 negatively regulates neurite outgrowth, making it a potential therapeutic target to promote axonal regeneration.
Rap1 是一种小 GTPase,它与树突发育和可塑性有关。在这项研究中,我们研究了 Rap1 在轴突生长中的作用及其对神经营养因子和髓鞘相关抑制剂的反应。我们报告说,Rap1 被脑源性神经营养因子激活,而这种激活可以被髓鞘相关糖蛋白 (MAG) 或中枢神经系统髓鞘阻断,这也导致 Rap1GAP1 水平增加。此外,我们证明,Rap1 的腺病毒过表达在 MAG 和髓鞘存在的情况下增强了神经突的生长,而通过 Rap1GAP1 的过表达抑制 Rap1 活性则阻止了神经突的生长。这些发现表明,Rap1GAP1 负调节神经突的生长,使其成为促进轴突再生的潜在治疗靶点。