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PMID: 12055633 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Synaptotagmin function in dense core vesicle exocytosis studied in cracked PC12 cells.

Nature neuroscience ·Vol. 5 ·No. 7 ·2002-07-00 ·Pages 649-56

Shin OH, Rizo J, Südhof TC

Abstract

Ca(2+)-triggered dense-core vesicle exocytosis in PC12 cells does not require vesicular synaptotagmins 1 and 2, but may use plasma membrane synaptotagmins 3 and 7 as Ca(2+) sensors. In support of this hypothesis, C(2) domains from the plasma membrane but not vesicular synaptotagmins inhibit PC12 cell exocytosis. Ca(2+) induces binding of both plasma membrane and vesicular synaptotagmins to phospholipids and SNAREs (soluble N-ethylmaleimide-sensitive attachment protein receptors), although with distinct apparent Ca(2+) affinities. Here we used gain-of-function C(2)-domain mutants of synaptotagmin 1 and loss-of-function C(2)-domain mutants of synaptotagmin 7 to examine how synaptotagmins function in dense-core vesicle exocytosis. Our data indicate that phospholipid- but not SNARE-binding by plasma membrane synaptotagmins is the primary determinant of Ca(2+)-triggered dense-core vesicle exocytosis. These results support a general lipid-based mechanism of action of synaptotagmins in exocytosis, with the specificity of various synaptotagmins for different types of fusion governed by their differential localizations and Ca(2+) affinities.

MeSH Terms
Animals Calcium/metabolism,pharmacology Calcium-Binding Proteins Cell Membrane Permeability/physiology Electrophoresis, Polyacrylamide Gel Exocytosis/drug effects,physiology Freezing Membrane Glycoproteins/genetics,metabolism Membrane Proteins/metabolism Mutagenesis, Site-Directed Nerve Tissue Proteins/genetics,metabolism PC12 Cells Phospholipids/metabolism Protein Binding/physiology Protein Structure, Tertiary/physiology Rats SNARE Proteins Secretory Vesicles/metabolism Structure-Activity Relationship Synaptotagmin I Synaptotagmins Vesicular Transport Proteins
Chemicals
Calcium-Binding Proteins Membrane Glycoproteins Membrane Proteins Nerve Tissue Proteins Phospholipids SNARE Proteins Synaptotagmin I Syt1 protein, rat Syt7 protein, rat Vesicular Transport Proteins Synaptotagmins Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Shin Ok-Ho
Center for Basic Neuroscience, Department of Molecular Genetics and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, 6000 Harry Hines Blvd., Dallas, Texas 75390, USA.
Rizo Josep
Südhof Thomas C
Article Info
Journal
Nature neuroscience
Abbr.
Nat Neurosci
ISSN
1097-6256
Published
2002-07-00
Pages
649-56
Language
English
Region
United States
NLM ID
9809671
Subset
IM
Grants
NINDS NIH HHS · NS37200 · United States
NINDS NIH HHS · NS40944 · United States
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