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PMID: 11228149 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Phosphoinositides in membrane traffic at the synapse.

Journal of cell science ·Vol. 114 ·No. Pt 6 ·2001-03-00 ·Pages 1041-52

Cremona O, De Camilli P

Abstract

Inositol phospholipids represent a minor fraction of membrane phospholipids; yet they play important regulatory functions in signaling pathways and membrane traffic. The phosphorylated inositol ring can act either as a precursor for soluble intracellular messengers or as a binding site for cytosolic or membrane proteins. Hence, phosphorylation-dephosphorylation of phosphoinositides represents a mechanism for regulation of recruitment to the membrane of coat proteins, cytoskeletal scaffolds or signaling complexes and for the regulation of membrane proteins. Recent work suggests that phosphoinositide metabolism has an important role in membrane traffic at the synapse. PtdIns(4,5)P2 generation is implicated in the secretion of at least a subset of neurotransmitters. Furthermore, PtdIns(4,5)P2 plays a role in the nucleation of clathrin coats and of an actin-based cytoskeletal scaffold at endocytic zones of synapses, and PtdIns(4,5)P2 dephosphorylation accompanies the release of newly formed vesicles from these interactions. Thus, the reversible phosphorylation of inositol phospholipids may be one of the mechanisms governing the timing and vectorial progression of synaptic vesicle membranes during their exocytic-endocytic cycle.

MeSH Terms
Actins/metabolism Animals Biological Transport Cell Membrane/metabolism,physiology Clathrin-Coated Vesicles/physiology Drosophila Endocytosis/physiology Exocytosis/physiology GTP Phosphohydrolases Humans Membrane Fusion Neurotransmitter Agents/metabolism Phosphatidylinositols/physiology Secretory Vesicles/physiology Synapses Synaptic Vesicles/physiology Yeasts
Chemicals
Actins Neurotransmitter Agents Phosphatidylinositols GTP Phosphohydrolases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cremona O
Department of Medical Sciences, Università del Piemonte Orientale 'A. Avogadro', Via Solaroli 17, Italy. cremona@med.unipmn.it
De Camilli P
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
2001-03-00
Pages
1041-52
Language
English
Region
England
NLM ID
0052457
Subset
IM
Grants
Telethon · D.111 · Italy
NCI NIH HHS · CA46128 · United States
NINDS NIH HHS · NS36251 · United States
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