HPC-1/syntaxin 1A suppresses exocytosis of PC12 cells.

Abstract:

:The membrane protein syntaxin (originally named HPC-1) is involved in vesicle trafficking and required for neurotransmitter release at nerve terminals. The presence of syntaxin on target membranes is hypothesized to confer specificity to targeting and fusion via interactions with complementary vesicle-associated proteins. To elucidate the function of syntaxin 1A in exocytosis, HPC-1/syntaxin 1A-reduced PC12h cells (PC12h/Deltasyx) that were stably transfected with a plasmid for antisense syntaxin 1A expression were constructed. Depolarizing stimulation of PC12h/Deltasyx enhanced dopamine release, compared with PC12h. There was a strong inverse correlation between syntaxin 1A protein expression and enhancement of dopamine release. Reduction of syntaxin 1A had no effect on increase of the cytoplasmic free Ca2+ concentration by depolarized stimulation. Moreover, PC12h/Deltasyx clones similarly enhanced of exocytosis by native secretagogues. These results indicate that syntaxin 1A has more than one function in exocytosis.

journal_name

J Biochem

journal_title

Journal of biochemistry

authors

Watanabe T,Fujiwara T,Komazaki S,Yamaguchi K,Tajima O,Akagawa K

doi

10.1093/oxfordjournals.jbchem.a022337

keywords:

subject

Has Abstract

pub_date

1999-04-01 00:00:00

pages

685-9

issue

4

eissn

0021-924X

issn

1756-2651

journal_volume

125

pub_type

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