Gasman Stéphane, Chasserot-Golaz Sylvette, Bader Marie-France, Vitale Nicolas
CNRS UPR-2356 Neurotransmission et Sécrétion Neuroendocrine, Centre de Neurochimie, 5 rue Blaise Pascal, 67084 Strasbourg, France.
Cell Signal. 2003 Oct;15(10):893-9. doi: 10.1016/s0898-6568(03)00052-4.
Neurons and neuroendocrine cells release transmitters and hormones by exocytosis, a highly regulated process in which secretory vesicles or granules fuse with the plasma membrane to release their contents in response to a calcium trigger. Several stages have been recognized in exocytosis. After recruitment and docking at the plasma membrane, vesicles/granules enter a priming step, which is then followed by the fusion process. Cortical actin remodelling accompanies the exocytotic reaction, but the links between actin dynamics and trafficking events remain poorly understood. Here, we review the action of Rho and ADP-ribosylation factor (ARF) GTPases within the exocytotic pathway in adrenal chromaffin cells. Rho proteins are well known for their pivotal role in regulating the actin cytoskeleton. ARFs were originally identified as regulators of vesicle transport within cells. The possible interplay between these two families of GTPases and their downstream effectors provides novel insights into the mechanisms that govern exocytosis.
神经元和神经内分泌细胞通过胞吐作用释放递质和激素,这是一个受到高度调控的过程,在此过程中,分泌囊泡或颗粒与质膜融合,以响应钙触发信号释放其内容物。胞吐作用已被识别出几个阶段。在被募集并停靠在质膜后,囊泡/颗粒进入一个引发步骤,随后是融合过程。皮质肌动蛋白重塑伴随着胞吐反应,但肌动蛋白动力学与运输事件之间的联系仍知之甚少。在这里,我们综述了Rho和ADP-核糖基化因子(ARF)小G蛋白在肾上腺嗜铬细胞胞吐途径中的作用。Rho蛋白因其在调节肌动蛋白细胞骨架中的关键作用而闻名。ARF最初被鉴定为细胞内囊泡运输的调节因子。这两类小G蛋白与其下游效应器之间可能的相互作用为控制胞吐作用的机制提供了新的见解。