Waters Joanne E, Astle Megan V, Ooms Lisa M, Balamatsias Demis, Gurung Rajendra, Mitchell Christina A
Department of Biochemistry and Molecular Biology, Monash University, Clayton 3800, Victoria, Australia.
J Cell Sci. 2008 Sep 1;121(Pt 17):2892-903. doi: 10.1242/jcs.030353. Epub 2008 Aug 12.
The Rac-GEF P-Rex1 promotes membrane ruffling and cell migration in response to Rac activation, but its role in neuritogenesis is unknown. Rac1 promotes neurite differentiation; Rac3, however, may play an opposing role. Here we report that in nerve growth factor (NGF)-differentiated rat PC12 cells, P-Rex1 localised to the distal tips of developing neurites and to the axonal shaft and growth cone of differentiating hippocampal neurons. P-Rex1 expression inhibited NGF-stimulated PC12 neurite differentiation and this was dependent on the Rac-GEF activity of P-Rex1. P-Rex1 inhibition of neurite outgrowth was rescued by low-dose cytochalasin D treatment, which prevents actin polymerisation. P-Rex1 activated Rac3 GTPase activity when coexpressed in PC12 cells. In the absence of NGF stimulation, targeted depletion of P-Rex1 in PC12 cells by RNA interference induced the spontaneous formation of beta-tubulin-enriched projections. Following NGF stimulation, enhanced neurite differentiation, with neurite hyper-elongation correlating with decreased F-actin at the growth cone, was demonstrated in P-Rex1 knockdown cells. Interestingly, P-Rex1-depleted PC12 cells exhibited reduced Rac3 and Rac1 GTPase activity. This study has identified P-Rex1 as a Rac3-GEF in neuronal cells that localises to, and regulates, actin cytoskeletal dynamics at the axonal growth cone to in turn regulate neurite differentiation.
Rac鸟嘌呤核苷酸交换因子P-Rex1可响应Rac激活促进膜皱襞形成和细胞迁移,但其在神经突发生中的作用尚不清楚。Rac1促进神经突分化;然而,Rac3可能起相反作用。在此我们报告,在神经生长因子(NGF)诱导分化的大鼠PC12细胞中,P-Rex1定位于正在发育的神经突的远端尖端以及分化的海马神经元的轴突干和生长锥。P-Rex1的表达抑制了NGF刺激的PC12神经突分化,这依赖于P-Rex1的Rac鸟嘌呤核苷酸交换因子活性。低剂量细胞松弛素D处理可挽救P-Rex1对神经突生长的抑制作用,该处理可阻止肌动蛋白聚合。当在PC12细胞中共表达时,P-Rex1激活Rac3 GTP酶活性。在无NGF刺激的情况下,通过RNA干扰在PC12细胞中靶向敲低P-Rex1可诱导富含β-微管蛋白的突起自发形成。在NGF刺激后,P-Rex1基因敲低的细胞表现出增强的神经突分化,神经突过度伸长与生长锥处F-肌动蛋白减少相关。有趣的是,P-Rex1缺失的PC12细胞表现出Rac3和Rac1 GTP酶活性降低。本研究已确定P-Rex1是神经元细胞中的一种Rac3鸟嘌呤核苷酸交换因子,其定位于轴突生长锥并调节肌动蛋白细胞骨架动力学,进而调节神经突分化。