Literature DB >> 9727496

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

Z Guo1, C Turner, D Castle.   

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.

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Year:  1998        PMID: 9727496     DOI: 10.1016/s0092-8674(00)81594-9

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  78 in total

1.  Phosphorylation of SNAP-23 by the novel kinase SNAK regulates t-SNARE complex assembly.

Authors:  J P Cabaniols; V Ravichandran; P A Roche
Journal:  Mol Biol Cell       Date:  1999-12       Impact factor: 4.138

2.  The secretory carrier membrane protein family: structure and membrane topology.

Authors:  C Hubbard; D Singleton; M Rauch; S Jayasinghe; D Cafiso; D Castle
Journal:  Mol Biol Cell       Date:  2000-09       Impact factor: 4.138

3.  Vimentin filaments in fibroblasts are a reservoir for SNAP23, a component of the membrane fusion machinery.

Authors:  W Faigle; E Colucci-Guyon; D Louvard; S Amigorena; T Galli
Journal:  Mol Biol Cell       Date:  2000-10       Impact factor: 4.138

4.  Identification and characterization of Snapin as a ubiquitously expressed SNARE-binding protein that interacts with SNAP23 in non-neuronal cells.

Authors:  Penelope Buxton; Xiang-Ming Zhang; Bong Walsh; Absorn Sriratana; Irina Schenberg; Elizabeth Manickam; Tony Rowe
Journal:  Biochem J       Date:  2003-10-15       Impact factor: 3.857

5.  Purification and identification of secernin, a novel cytosolic protein that regulates exocytosis in mast cells.

Authors:  Gemma Way; Nicholas Morrice; Carl Smythe; Antony J O'Sullivan
Journal:  Mol Biol Cell       Date:  2002-09       Impact factor: 4.138

6.  Molecular control of compound Exocytosis: A key role for VAMP8.

Authors:  Peter Thorn; Herbert Gaisano
Journal:  Commun Integr Biol       Date:  2012-01-01

7.  Sequential compound exocytosis of large dense-core vesicles in PC12 cells studied with TEPIQ (two-photon extracellular polar-tracer imaging-based quantification) analysis.

Authors:  Takuya Kishimoto; Ting-Ting Liu; Hiroyasu Hatakeyama; Tomomi Nemoto; Noriko Takahashi; Haruo Kasai
Journal:  J Physiol       Date:  2005-09-08       Impact factor: 5.182

8.  Central nervous system neurons acquire mast cell products via transgranulation.

Authors:  M Wilhelm; R Silver; A J Silverman
Journal:  Eur J Neurosci       Date:  2005-11       Impact factor: 3.386

9.  Munc18-2 and syntaxin 3 control distinct essential steps in mast cell degranulation.

Authors:  Cristiana Brochetta; Ryo Suzuki; Francesca Vita; Maria Rosa Soranzo; Julien Claver; Lydia Celia Madjene; Tarik Attout; Joana Vitte; Nadine Varin-Blank; Giuliano Zabucchi; Juan Rivera; Ulrich Blank
Journal:  J Immunol       Date:  2013-12-09       Impact factor: 5.422

10.  Polyphenols differentially inhibit degranulation of distinct subsets of vesicles in mast cells by specific interaction with granule-type-dependent SNARE complexes.

Authors:  Yoosoo Yang; Jung-Mi Oh; Paul Heo; Jae Yoon Shin; Byoungjae Kong; Jonghyeok Shin; Ji-Chun Lee; Jeong Su Oh; Kye Won Park; Choong Hwan Lee; Yeon-Kyun Shin; Dae-Hyuk Kweon
Journal:  Biochem J       Date:  2013-03-15       Impact factor: 3.857

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