Literature DB >> 3253299

Diacylglycerol-induced shape changes, movements and altered F-actin distribution in human neutrophils.

A Zimmermann1, P Gehr, H U Keller.   

Abstract

The study shows that diacylglycerols (DAGs) as physiological activators of protein kinase C induce characteristic shape changes in human neutrophil granulocytes. In contrast to chemotactic peptides, which can induce front-tail polarity characterized by a contracted tail and an expanding front, DAGs elicit the formation of non-polar cells with surface projections. These cells exhibit a distinct type of motility characterized by vigorous and continuous shape changes without front-tail polarity and without the unidirectional movement and cytoplasmic streaming seen in polarized cells. In neutrophils exposed to DAGs, F-actin is shifted to the cell periphery and mainly into the surface projections of activated cells. DAGs induce the formation of large intracellular vacuoles in neutrophils producing surface projections, and these vacuoles persist after the cells have reacquired a spherical shape. Combined stimulation of human neutrophils with DAG and fNLPNTL results in a suppression of peptide-induced polarity and the formation of non-polar motile cells resembling those stimulated with DAG alone. These results suggest that the diacylglycerol-protein kinase C pathway may be instrumental in transducing or modulating signals to both the locomotor apparatus and the exocytotic and/or pinocytic system of the cell. Neutrophil stimulation with DAGs thus represents a useful model with which to study further the hypothesis that distinct types of neutrophil shapes and movements are preferentially associated with distinct functions and to characterize signalling pathways.

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Year:  1988        PMID: 3253299     DOI: 10.1242/jcs.90.4.657

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  7 in total

1.  Protein phosphorylation by protein kinase C in HEp-2 cells infected with enteropathogenic Escherichia coli.

Authors:  T J Baldwin; S F Brooks; S Knutton; H A Manjarrez Hernandez; A Aitken; P H Williams
Journal:  Infect Immun       Date:  1990-03       Impact factor: 3.441

2.  Reduction by inhibitors of mono(ADP-ribosyl)transferase of chemotaxis in human neutrophil leucocytes by inhibition of the assembly of filamentous actin.

Authors:  J R Allport; L E Donnelly; B P Hayes; S Murray; N B Rendell; K P Ray; J MacDermot
Journal:  Br J Pharmacol       Date:  1996-07       Impact factor: 8.739

3.  Phorbol myristate acetate induction of chemotactic migration of human polymorphonuclear neutrophils.

Authors:  W L Gabler; W W Bullock; H R Creamer
Journal:  Inflammation       Date:  1993-08       Impact factor: 4.092

4.  Myristoylated alanine-rich C-kinase substrate (MARCKS) protein regulation of human neutrophil migration.

Authors:  Rachael E Eckert; Laura E Neuder; Joungjoa Park; Kenneth B Adler; Samuel L Jones
Journal:  Am J Respir Cell Mol Biol       Date:  2009-07-02       Impact factor: 6.914

5.  Mechanism of inhibition of cyclic nucleotide-gated ion channels by diacylglycerol.

Authors:  J I Crary; D M Dean; W Nguitragool; P T Kurshan; A L Zimmerman
Journal:  J Gen Physiol       Date:  2000-12       Impact factor: 4.086

6.  Mediation of chemoattractant-induced changes in [Ca2+]i and cell shape, polarity, and locomotion by InsP3, DAG, and protein kinase C in newt eosinophils.

Authors:  S H Gilbert; K Perry; F S Fay
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

7.  Effects of staurosporine, K 252a and other structurally related protein kinase inhibitors on shape and locomotion of Walker carcinosarcoma cells.

Authors:  A Zimmermann; H Keller
Journal:  Br J Cancer       Date:  1992-12       Impact factor: 7.640

  7 in total

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