Literature DB >> 8626670

Evidence that syntaxin 1A is involved in storage in the secretory pathway.

M A Bittner1, M K Bennett, R W Holz.   

Abstract

Syntaxin 1A is a nervous system-specific protein thought to function during the late steps of the regulated secretory pathway by mediating the docking of secretory vesicles with the plasma membrane. We have examined the effects of transiently overexpressing syntaxin 1A on protein secretion in constitutively secreting cell lines that do not normally express the protein. Syntaxin 1A showed the constitutive release of marker proteins human growth hormone (hGH) and vesicular stomatitis virus glycoprotein from COS-1 cells, increasing the intracellular half-life of human growth hormone from 90 min to 18 h. A similar effect was observed in HEK 293 cells. Immunofluorescence microscopy revealed that these secretory proteins were concentrated in the periphery of the cell. The effect was specific for the full-length neuronal protein. Neither a syntaxin 1A variant which lacks a membrane attachment domain nor syntaxin 2 caused the cells to retain human growth hormone. The effect of syntaxin 1A was partially reversed by incubating the cells with botulinum type C1 neurotoxin, which specifically cleaves syntaxin 1A. Release of human growth hormone from syntaxin 1A-expressing cells was maintained during a blockade of protein synthesis, suggesting that the hormone was being released from a pool of stored vesicles which accumulated before the addition of cycloheximide. The existence of a post-Golgi storage compartment in syntaxin 1A-expressing cells was confirmed using brefeldin A to collapse the Golgi stacks in both HEK 293 and COS-1 cells. Brefeldin A rapidly blocked growth hormone release in control cultures while having no effect on release in cells expressing syntaxin 1A. Reducing the temperature to 19 degrees C, which inhibits transport from the trans-Golgi network, also inhibited hGH secretion from cells without syntaxin 1A but had little effect on hGH secretion from cells with syntaxin 1A. The present experiments indicate that syntaxin 1A enables the storage of vesicles which would otherwise be immediately released.

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Year:  1996        PMID: 8626670     DOI: 10.1074/jbc.271.19.11214

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

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2.  Biochemical and functional studies of cortical vesicle fusion: the SNARE complex and Ca2+ sensitivity.

Authors:  J R Coorssen; P S Blank; M Tahara; J Zimmerberg
Journal:  J Cell Biol       Date:  1998-12-28       Impact factor: 10.539

3.  A Ca2+-independent receptor for alpha-latrotoxin, CIRL, mediates effects on secretion via multiple mechanisms.

Authors:  M A Bittner; V G Krasnoperov; E L Stuenkel; A G Petrenko; R W Holz
Journal:  J Neurosci       Date:  1998-04-15       Impact factor: 6.167

4.  ROP, the Drosophila Sec1 homolog, interacts with syntaxin and regulates neurotransmitter release in a dosage-dependent manner.

Authors:  M N Wu; J T Littleton; M A Bhat; A Prokop; H J Bellen
Journal:  EMBO J       Date:  1998-01-02       Impact factor: 11.598

5.  Apoptotic surface delivery of K+ channels.

Authors:  S K Pal; K Takimoto; E Aizenman; E S Levitan
Journal:  Cell Death Differ       Date:  2006-04       Impact factor: 15.828

6.  Syntaxin-3 and syntaxin-1A inhibit L-type calcium channel activity, insulin biosynthesis and exocytosis in beta-cell lines.

Authors:  Y Kang; X Huang; E A Pasyk; J Ji; G G Holz; M B Wheeler; R G Tsushima; H Y Gaisano
Journal:  Diabetologia       Date:  2002-02       Impact factor: 10.122

7.  Differential expression of syntaxin 1A and 1B by noradrenergic and adrenergic chromaffin cells.

Authors:  Graça Baltazar; Arsélio P Carvalho; Emília P Duarte
Journal:  Neurochem Res       Date:  2003-10       Impact factor: 3.996

8.  Geranylgeranylated SNAREs are dominant inhibitors of membrane fusion.

Authors:  E Grote; M Baba; Y Ohsumi; P J Novick
Journal:  J Cell Biol       Date:  2000-10-16       Impact factor: 10.539

9.  A novel function for SNAP29 (synaptosomal-associated protein of 29 kDa) in mast cell phagocytosis.

Authors:  Jordan Wesolowski; Vernon Caldwell; Fabienne Paumet
Journal:  PLoS One       Date:  2012-11-21       Impact factor: 3.240

  9 in total

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