Mariot P, O'Sullivan A J, Brown A M, Tatham P E
Department of Physiology, University College London, UK.
EMBO J. 1996 Dec 2;15(23):6476-82.
Introducing non-hydrolysable analogues of GTP into the cytosolic compartment of mast cells results in exocytotic secretion through the activation of GTP binding proteins. The identity and mechanism of action of these proteins are not established. We have investigated the effects of Rho GDP dissociation inhibitor (RhoGDI) on exocytosis induced by guanosine 5'-O-(3-thiotriphosphate) (GTP-gamma-S) in rat mast cells, introducing the protein into cells by means of a patch pipette and recording the progress of exocytosis by monitoring cell capacitance. To allow time for the protein to enter the cells and find its correct location, stimulation was provided 5-10 min after patch rupture by photolysing caged GTP-gamma-S included in the pipette solution. When bovine RhoGDI was introduced into mast cells, exocytosis was inhibited at concentrations of 200-400 nM for native protein and 800 nM to 8 microM for the recombinant form. Protein denatured by heat or N-ethylmaleimide treatment did not inhibit. In permeabilized cells, recombinant RhoGDI increased the rate at which cells lose their ability to respond to GTP-gamma-S. These data demonstrate that one or more small GTP binding proteins of the Rho family has a central role in the exocytotic mechanism in mast cells.
将不可水解的GTP类似物引入肥大细胞的胞质区室,会通过激活GTP结合蛋白导致胞吐分泌。这些蛋白的身份和作用机制尚未明确。我们研究了Rho GDP解离抑制剂(RhoGDI)对大鼠肥大细胞中由鸟苷5'-O-(3-硫代三磷酸)(GTP-γ-S)诱导的胞吐作用的影响,通过膜片移液管将该蛋白引入细胞,并通过监测细胞电容记录胞吐作用的进程。为了给蛋白进入细胞并找到其正确位置留出时间,在膜片破裂5-10分钟后,通过光裂解移液管溶液中包含的笼锁GTP-γ-S来提供刺激。当将牛RhoGDI引入肥大细胞时,对于天然蛋白,浓度为200-400 nM时胞吐作用受到抑制,对于重组形式,浓度为800 nM至8 μM时胞吐作用受到抑制。经加热或N-乙基马来酰亚胺处理变性的蛋白没有抑制作用。在透化细胞中,重组RhoGDI提高了细胞丧失对GTP-γ-S反应能力的速率。这些数据表明,Rho家族的一种或多种小GTP结合蛋白在肥大细胞的胞吐机制中起核心作用。