Literature DB >> 1918158

Kinetic analysis of F-actin depolymerization in polymorphonuclear leukocyte lysates indicates that chemoattractant stimulation increases actin filament number without altering the filament length distribution.

M L Cano1, D A Lauffenburger, S H Zigmond.   

Abstract

The rate of filamentous actin (F-actin) depolymerization is proportional to the number of filaments depolarizing and changes in the rate are proportional to changes in filament number. To determine the number and length of actin filaments in polymorphonuclear leukocytes and the change in filament number and length that occurs during the increase in F-actin upon chemoattractant stimulation, the time course of cellular F-actin depolymerization in lysates of control and peptide-stimulated cells was examined. F-actin was quantified by the TRITC-labeled phalloidin staining of pelletable actin. Lysis in 1.2 M KCl and 10 microM DNase I minimized the effects of F-actin binding proteins and G-actin, respectively, on the kinetics of depolymerization. To determine filament number and length from a depolymerization time course, depolymerization kinetics must be limited by the actin monomer dissociation rate. Comparison of time courses of depolymerization in the presence (pointed ends free) or absence (barbed and pointed ends free) of cytochalasin suggested depolymerization occurred from both ends of the filament and that monomer dissociation was rate limiting. Control cells had 1.7 +/- 0.4 x 10(5) filaments with an average length of 0.29 +/- 0.09 microns. Chemo-attractant stimulation for 90 s at room temperature with 0.02 microM N-formylnorleucylleucylphenylalanine caused a twofold increase in F-actin and about a two-fold increase in the total number of actin filaments to 4.0 +/- 0.5 x 10(5) filaments with an average length of 0.27 +/- 0.07 microns. In both cases, most (approximately 80%) of the filaments were quite short (less than or equal to 0.18 micron). The length distributions of actin filaments in stimulated and control cells were similar.

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Year:  1991        PMID: 1918158      PMCID: PMC2289167          DOI: 10.1083/jcb.115.3.677

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  35 in total

1.  Tropomyosin prevents depolymerization of actin filaments from the pointed end.

Authors:  K O Broschat
Journal:  J Biol Chem       Date:  1990-12-05       Impact factor: 5.157

2.  Tropomyosin stabilizes the pointed end of actin filaments by slowing depolymerization.

Authors:  K O Broschat; A Weber; D R Burgess
Journal:  Biochemistry       Date:  1989-10-17       Impact factor: 3.162

3.  Different calcium dependence of the capping and cutting activities of villin.

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Journal:  J Biol Chem       Date:  1986-07-15       Impact factor: 5.157

4.  Effect of muscle tropomyosin on the kinetics of polymerization of muscle actin.

Authors:  A A Lal; E D Korn
Journal:  Biochemistry       Date:  1986-03-11       Impact factor: 3.162

5.  Tropomyosin in the sea urchin egg cortex.

Authors:  S Maekawa; M Toriyama; H Sakai
Journal:  Eur J Biochem       Date:  1989-01-02

6.  Kinetic analysis of microtubule self-assembly in vitro.

Authors:  K A Johnson; G G Borisy
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Review 7.  The organization and regulation of the macrophage actin skeleton.

Authors:  J H Hartwig; H L Yin
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8.  Low Mr tropomyosin isoforms from chicken brain and intestinal epithelium have distinct actin-binding properties.

Authors:  K O Broschat; D R Burgess
Journal:  J Biol Chem       Date:  1986-10-05       Impact factor: 5.157

9.  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

Review 10.  Effects of cytochalasin and phalloidin on actin.

Authors:  J A Cooper
Journal:  J Cell Biol       Date:  1987-10       Impact factor: 10.539

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  41 in total

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7.  Actin polymerization stimulated by contractile activation regulates force development in canine tracheal smooth muscle.

Authors:  D Mehta; S J Gunst
Journal:  J Physiol       Date:  1999-09-15       Impact factor: 5.182

8.  Mapping the binding site of thymosin beta4 on actin by competition with G-actin binding proteins indicates negative co-operativity between binding sites located on opposite subdomains of actin.

Authors:  E Ballweber; E Hannappel; T Huff; H G Mannherz
Journal:  Biochem J       Date:  1997-11-01       Impact factor: 3.857

9.  Mechanism of Cdc42-induced actin polymerization in neutrophil extracts.

Authors:  S H Zigmond; M Joyce; C Yang; K Brown; M Huang; M Pring
Journal:  J Cell Biol       Date:  1998-08-24       Impact factor: 10.539

10.  ADP-ribosylation of the GTP-binding protein Rho by Clostridium limosum exoenzyme affects basal, but not N-formyl-peptide-stimulated, actin polymerization in human myeloid leukaemic (HL60) cells.

Authors:  G Koch; J Norgauer; K Aktories
Journal:  Biochem J       Date:  1994-05-01       Impact factor: 3.857

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