Signal transduction in neutrophil chemotaxis.

Details

Serval ID
serval:BIB_499D376C3E81
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Title
Signal transduction in neutrophil chemotaxis.
Journal
Biochemistry
Author(s)
Katanaev V.L.
ISSN
0006-2979 (Print)
ISSN-L
0006-2979
Publication state
Published
Issued date
2001
Volume
66
Number
4
Pages
351-368
Language
english
Abstract
This review discusses current knowledge on signal transduction pathways controlling chemotaxis of neutrophils and similar cells. Most neutrophil chemoattractants bind to seven-transmembrane-helix receptors. These receptors activate trimeric G proteins of the Gi class in neutrophils to initiate chemotaxis. Phospholipases Cbeta, phosphoinositide 3-kinase gamma, and PH domain-containing proteins play various roles in signaling further downstream. The actin cytoskeleton is crucial for cell motility, and is controlled by Rho family GTP-binding proteins. PIP 5-kinase, LIM kinase, myosin light chain kinase and phosphatase, or WASP-like proteins may be important links between Rho GTPases and actin during chemotaxis. Newly emerging ideas on the regulation of the "compass" of chemotaxing cells, which may involve Cdc42 and certain PH domain-containing proteins, are also presented.
Keywords
Animals, Cell Movement/physiology, Chemotactic Factors/physiology, Chemotaxis, Leukocyte/physiology, GTP-Binding Proteins/chemistry, GTP-Binding Proteins/metabolism, Humans, Neutrophils/cytology, Neutrophils/metabolism, Phosphatidylinositol 3-Kinases/metabolism, Receptors, Formyl Peptide, Receptors, Immunologic/chemistry, Receptors, Immunologic/metabolism, Receptors, Peptide/chemistry, Receptors, Peptide/metabolism, Signal Transduction/physiology, cdc42 GTP-Binding Protein/physiology, rho GTP-Binding Proteins/physiology
Pubmed
Web of science
Create date
09/07/2012 10:09
Last modification date
20/08/2019 14:57
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