Literature DB >> 1337290

Role of gelsolin interaction with actin in regulation and creation of actin nuclei in chemotactic peptide activated polymorphonuclear neutrophils.

J D Deaton1, T Guerrero, T H Howard.   

Abstract

In vitro Ca++ activates gelsolin to sever F-actin and form a gelsolin-actin (GA) complex at the+end of F-actin that is not dissociated by ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA) but is separated by EGTA+PIP/PIP2. The gelsolin blocks the+end on the actin filament, but the-end of the filament can still initiate actin polymerization. In thrombin activated platelets, evidence suggests that severing of F-actin by gelsolin increases GA complex, creates one-end actin nucleus and one cryptic+end actin nucleus per cut, and then dissociates to yield free+ends to nucleate rapid actin assembly. We examined the role of F-actin severing in creation and regulation of nuclei and polymerization in polymorphonuclear neutrophils (PMNs). At 2-s intervals after formyl peptide (FMLP) activation of endotoxin free (ETF) PMNs, change in GA complex was correlated with change in+end actin nuclei,-end actin nuclei, and F-actin content. GA complex was quantitated by electrophoretograms of proteins absorbed by antigelsolin from cells lysed in 10 mM EGTA,+end actin nuclei as cytochalasin (CD) sensitive and-end actin nuclei as CD insensitive increases in G-pyrenyl actin polymerization rates induced by the same PMNs, and F-actin content by NBDphallacidin binding to fixed cells. Thirty three percent of gelsolin was in GA complex in basal ETF PMNs; from 2-6 s, GA complexes dissociate (low = 15% at 10 s) and sequentially+end nuclei and F-actin content and then-end nuclei increase to a maximum at 10 s. At > s GA complex increase toward basal and + end nuclei and F-actin content returned toward basal. These kinetic data show gelsolin regulates availability of + end nuclei and actin polymerization in FMLP. However, absence of an initial increase in GA complex or - end nucleating activity shows FMLP activation does not cause gelsolin to sever F- or to bind G-actin to create cryptic + end nuclei in PMNs; the results suggest the + nucleus formation is gelsolin independent.

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Year:  1992        PMID: 1337290      PMCID: PMC275710          DOI: 10.1091/mbc.3.12.1427

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  46 in total

1.  Functional comparison of villin and gelsolin. Effects of Ca2+, KCl, and polyphosphoinositides.

Authors:  P A Janmey; P T Matsudaira
Journal:  J Biol Chem       Date:  1988-11-15       Impact factor: 5.157

2.  Rabbit alveolar macrophages contain a Ca2+-sensitive, 41,000-dalton protein which reversibly blocks the "barbed" ends of actin filaments but does not sever them.

Authors:  F S Southwick; M J DiNubile
Journal:  J Biol Chem       Date:  1986-10-25       Impact factor: 5.157

Review 3.  Actin and actin-binding proteins. A critical evaluation of mechanisms and functions.

Authors:  T D Pollard; J A Cooper
Journal:  Annu Rev Biochem       Date:  1986       Impact factor: 23.643

4.  Polyphosphoinositide micelles and polyphosphoinositide-containing vesicles dissociate endogenous gelsolin-actin complexes and promote actin assembly from the fast-growing end of actin filaments blocked by gelsolin.

Authors:  P A Janmey; K Iida; H L Yin; T P Stossel
Journal:  J Biol Chem       Date:  1987-09-05       Impact factor: 5.157

5.  Modulation of multiple neutrophil functions by preparative methods or trace concentrations of bacterial lipopolysaccharide.

Authors:  C Haslett; L A Guthrie; M M Kopaniak; R B Johnston; P M Henson
Journal:  Am J Pathol       Date:  1985-04       Impact factor: 4.307

6.  gCap39, a calcium ion- and polyphosphoinositide-regulated actin capping protein.

Authors:  F X Yu; P A Johnston; T C Südhof; H L Yin
Journal:  Science       Date:  1990-12-07       Impact factor: 47.728

7.  A domain of synapsin I involved with actin bundling shares immunologic cross-reactivity with villin.

Authors:  T C Petrucci; M S Mooseker; J S Morrow
Journal:  J Cell Biochem       Date:  1988-01       Impact factor: 4.429

8.  An actin-nucleating activity in polymorphonuclear leukocytes is modulated by chemotactic peptides.

Authors:  M Carson; A Weber; S H Zigmond
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

9.  Reversibility of gelsolin/actin interaction in macrophages. Evidence of Ca2+-dependent and Ca2+-independent pathways.

Authors:  C Chaponnier; H L Yin; T P Stossel
Journal:  J Exp Med       Date:  1987-01-01       Impact factor: 14.307

10.  Dictyostelium discoideum plasma membranes contain an actin-nucleating activity that requires ponticulin, an integral membrane glycoprotein.

Authors:  A Shariff; E J Luna
Journal:  J Cell Biol       Date:  1990-03       Impact factor: 10.539

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  1 in total

Review 1.  Bench to Bedside: Proteomic Biomarker Analysis of Cerebrospinal Fluid in Patients With Spondylomyelopathy.

Authors:  Brian Fiani; Claudia Covarrubias; Ryan Jarrah
Journal:  Cureus       Date:  2021-06-28
  1 in total

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