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t-SNARE蛋白SNAP-23从类板状伪足样细胞表面突起的重新定位调节肥大细胞中的复合胞吐作用。

Relocation of the t-SNARE SNAP-23 from lamellipodia-like cell surface projections regulates compound exocytosis in mast cells.

作者信息

Guo Z, Turner C, Castle D

机构信息

Department of Cell Biology, University of Virgina Health Sciences Center, Charlottesville 22908, USA.

出版信息

Cell. 1998 Aug 21;94(4):537-48. doi: 10.1016/s0092-8674(00)81594-9.

Abstract

For regulated secretion, mast cells and several other cell types utilize compound exocytosis, a combination of granule-plasma membrane and granule-granule fusions. The molecular machinery that controls this massive export process has not been identified. We report that SNAP-23, a t-SNARE related to SNAP-25, relocates in response to stimulation from plasma membrane lamellipodia-like projections to granule membranes in permeabilized mast cells. While relocation is a prerequisite for secretion, it can occur without membrane fusion and will expedite a subsequent secretory response. After relocation, SNAP-23 is required for exocytosis, implying a crucial role in promoting membrane fusion. Thus, relocation of this SNARE regulates compound exocytosis and links granule-plasma membrane and granule-granule fusions.

摘要

对于受调控的分泌,肥大细胞和其他几种细胞类型利用复合胞吐作用,即颗粒-质膜融合与颗粒-颗粒融合的结合。控制这一大量物质输出过程的分子机制尚未明确。我们报告称,与SNAP-25相关的t-SNARE蛋白SNAP-23,在通透的肥大细胞中,会响应来自质膜片状伪足样突起的刺激而重新定位到颗粒膜上。虽然重新定位是分泌的一个先决条件,但它可以在没有膜融合的情况下发生,并且会加速随后的分泌反应。重新定位后,胞吐作用需要SNAP-23,这意味着它在促进膜融合中起关键作用。因此,这种SNARE蛋白的重新定位调节复合胞吐作用,并将颗粒-质膜融合与颗粒-颗粒融合联系起来。

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