Model Animal Research Center, State Key Laboratory of Pharmaceutical Biotechnology, Department of Neurology of the Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, Nanjing University, Nanjing 210061, China and.
Department of Medicine, University of Wisconsin-Madison, Madison, Wisconsin 53706.
J Biol Chem. 2019 Jul 12;294(28):10954-10968. doi: 10.1074/jbc.RA118.007318. Epub 2019 May 31.
Neurite outgrowth requires coordinated cytoskeletal rearrangements in the growth cone and directional membrane delivery from the neuronal soma. As an essential Rho guanine nucleotide exchange factor (GEF), TRIO is necessary for cytoskeletal dynamics during neurite outgrowth, but its participation in the membrane delivery is unclear. Using co-localization studies, live-cell imaging, and fluorescence recovery after photobleaching analysis, along with neurite outgrowth assay and various biochemical approaches, we here report that in mouse cerebellar granule neurons, TRIO protein pools at the Golgi and regulates membrane trafficking by controlling the directional maintenance of both RAB8 (member RAS oncogene family 8)- and RAB10-positive membrane vesicles. We found that the spectrin repeats in Golgi-resident TRIO confer RAB8 and RAB10 activation by interacting with and activating the RAB GEF RABIN8. Constitutively active RAB8 or RAB10 could partially restore the neurite outgrowth of TRIO-deficient cerebellar granule neurons, suggesting that TRIO-regulated membrane trafficking has an important functional role in neurite outgrowth. Our results also suggest cross-talk between Rho GEF and Rab GEF in controlling both cytoskeletal dynamics and membrane trafficking during neuronal development. They further highlight how protein pools localized to specific organelles regulate crucial cellular activities and functions. In conclusion, our findings indicate that TRIO regulates membrane trafficking during neurite outgrowth in coordination with its GEF-dependent function in controlling cytoskeletal dynamics via Rho GTPases.
神经突生长需要生长锥中细胞骨架的协调重排和来自神经元胞体的定向膜运输。作为一种必需的 Rho 鸟嘌呤核苷酸交换因子(GEF),TRIO 对于神经突生长过程中的细胞骨架动力学是必要的,但它在膜运输中的参与尚不清楚。通过共定位研究、活细胞成像和光漂白后荧光恢复分析,以及神经突生长测定和各种生化方法,我们在这里报告,在小鼠小脑颗粒神经元中,TRIO 蛋白在高尔基体中聚集,并通过控制 RAB8(RAS 癌基因家族 8 成员)和 RAB10 阳性膜囊泡的定向维持来调节膜运输。我们发现,高尔基体驻留的 TRIO 中的 spectrin 重复序列通过与 RAB GEF RABIN8 相互作用并激活它来激活 RAB8 和 RAB10。组成性激活的 RAB8 或 RAB10 可以部分恢复 TRIO 缺陷型小脑颗粒神经元的神经突生长,这表明 TRIO 调节的膜运输在神经突生长中具有重要的功能作用。我们的结果还表明,Rho GEF 和 Rab GEF 之间存在交叉对话,以控制神经元发育过程中的细胞骨架动力学和膜运输。它们进一步强调了定位于特定细胞器的蛋白质池如何调节关键的细胞活动和功能。总之,我们的发现表明,TRIO 通过其在控制 Rho GTPases 依赖性细胞骨架动力学中的 GEF 功能与协调膜运输,调节神经突生长过程中的膜运输。