Literature DB >> 1993736

Beta actin and its mRNA are localized at the plasma membrane and the regions of moving cytoplasm during the cellular response to injury.

T C Hoock1, P M Newcomb, I M Herman.   

Abstract

Previous work in our laboratory has shown that microvascular pericytes sort muscle and nonmuscle actin isoforms into discrete cytoplasmic domains (Herman, I. M., and P. A. D'Amore. 1985. J. Cell Biol. 101:43-52; DeNofrio, D.T.C. Hoock, and I. M. Herman. J. Cell. Biol. 109:191-202). Specifically, muscle (alpha-smooth) actin is present on the stress fibers while nonmuscle actins (beta and gamma) are located on stress fibers and in regions of moving cytoplasm (e.g., ruffles, lamellae). To determine the form and function of beta actin in microvascular pericytes and endothelial cells recovering from injury, we prepared isoform-specific antibodies and cDNA probes for immunolocalization, Western and Northern blotting, as well as in situ hybridization. Anti-beta actin IgG was prepared by adsorption and release of beta actin-specific IgG from electrophoretically purified pericyte beta actin bound to nitrocellulose paper. Anti-beta actin IgGs prepared by this affinity selection procedure showed exclusive binding to beta actin present in crude cell lysates containing all three actin isoforms. For controls, we localized beta actin as a bright rim of staining beneath the erythrocyte plasma membrane. Anti-beta actin IgG, absorbed with beta actin bound to nitrocellulose, failed to stain erythrocytes. Simultaneous localization of beta actin with the entire F-actin pool was performed on microvascular pericytes or endothelial cells and 3T3 fibroblasts recovering from injury using anti-beta actin IgG in combination with fluorescent phalloidin. Results of these experiments revealed that pericyte beta actin is localized beneath the plasma membrane in association with filopods, pseudopods, and fan lamellae. Additionally, we observed bright focal fluorescence within fan lamellae and in association with the ends of stress fibers that are preferentially associated with the ventral plasmalemma. Whereas fluorescent phalloidin staining along the stress fibers is continuous, anti-beta actin IgG localization is discontinuous. When injured endothelial and 3T3 cells were stained through wound closure, we localized beta actin only in motile cytoplasm at the wound edge. Staining disappeared as cells became quiescent upon monolayer restoration. Appearance of beta actin at the wound edge correlated with a two- to threefold increase in steady-state levels of beta actin mRNA, which rose within 15-60 min after injury and returned to noninjury levels during monolayer restoration. In situ hybridization revealed that transcripts encoding beta actin were localized at the wound edge in association with the repositioned protein. Results of these experiments indicate that beta actin and its encoded mRNA are polarized at the membrane-cytoskeletal interface within regions of moving cytoplasm.

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Year:  1991        PMID: 1993736      PMCID: PMC2288855          DOI: 10.1083/jcb.112.4.653

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


  62 in total

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Authors:  J Leavitt; G Bushar; T Kakunaga; H Hamada; T Hirakawa; D Goldman; C Merril
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2.  Subcellular sorting of isoactins: selective association of gamma actin with skeletal muscle mitochondria.

Authors:  J V Pardo; M F Pittenger; S W Craig
Journal:  Cell       Date:  1983-04       Impact factor: 41.582

3.  Actin expression in smooth muscle cells of rat aortic intimal thickening, human atheromatous plaque, and cultured rat aortic media.

Authors:  G Gabbiani; O Kocher; W S Bloom; J Vandekerckhove; K Weber
Journal:  J Clin Invest       Date:  1984-01       Impact factor: 14.808

4.  Isolation of microtubule protein from chicken erythrocytes and determination of the critical concentration for tubulin polymerization in vitro and in vivo.

Authors:  D B Murphy; K T Wallis
Journal:  J Biol Chem       Date:  1983-07-10       Impact factor: 5.157

5.  Gamma actin, spectrin, and intermediate filament proteins colocalize with vinculin at costameres, myofibril-to-sarcolemma attachment sites.

Authors:  S W Craig; J V Pardo
Journal:  Cell Motil       Date:  1983

6.  Gene switching in myogenesis: differential expression of the chicken actin multigene family.

Authors:  R J Schwartz; K N Rothblum
Journal:  Biochemistry       Date:  1981-07-07       Impact factor: 3.162

7.  The polymeric state of actin in the human erythrocyte cytoskeleton.

Authors:  M A Atkinson; J S Morrow; V T Marchesi
Journal:  J Cell Biochem       Date:  1982       Impact factor: 4.429

8.  An activated form of transforming growth factor beta is produced by cocultures of endothelial cells and pericytes.

Authors:  A Antonelli-Orlidge; K B Saunders; S R Smith; P A D'Amore
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

9.  The role of band 4.1 in the association of actin with erythrocyte membranes.

Authors:  C M Cohen; S F Foley
Journal:  Biochim Biophys Acta       Date:  1982-06-28

10.  Structural and dynamic states of actin in the erythrocyte.

Authors:  J C Pinder; W B Gratzer
Journal:  J Cell Biol       Date:  1983-03       Impact factor: 10.539

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  66 in total

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Authors:  Gang Liu; Wayne M Grant; Daniel Persky; Vaughan M Latham; Robert H Singer; John Condeelis
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2.  Betacap73-ARF6 interactions modulate cell shape and motility after injury in vitro.

Authors:  Kathleen N Riley; Angel E Maldonado; Patrice Tellier; Crislyn D'Souza-Schorey; Ira M Herman
Journal:  Mol Biol Cell       Date:  2003-07-11       Impact factor: 4.138

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Journal:  J Biol Chem       Date:  2003-05-22       Impact factor: 5.157

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Journal:  Mol Cell Proteomics       Date:  2012-03-22       Impact factor: 5.911

5.  The RNA-binding protein HuR promotes cell migration and cell invasion by stabilizing the beta-actin mRNA in a U-rich-element-dependent manner.

Authors:  Virginie Dormoy-Raclet; Isabelle Ménard; Eveline Clair; Ghada Kurban; Rachid Mazroui; Sergio Di Marco; Christopher von Roretz; Arnim Pause; Imed-Eddine Gallouzi
Journal:  Mol Cell Biol       Date:  2007-06-04       Impact factor: 4.272

6.  The large subunit of HIV-1 reverse transcriptase interacts with beta-actin.

Authors:  M Hottiger; K Gramatikoff; O Georgiev; C Chaponnier; W Schaffner; U Hübscher
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7.  Resorption-cycle-dependent polarization of mRNAs for different subunits of V-ATPase in bone-resorbing osteoclasts.

Authors:  T Laitala-Leinonen; M L Howell; G E Dean; H K Väänänen
Journal:  Mol Biol Cell       Date:  1996-01       Impact factor: 4.138

8.  Characterization of a beta-actin mRNA zipcode-binding protein.

Authors:  A F Ross; Y Oleynikov; E H Kislauskis; K L Taneja; R H Singer
Journal:  Mol Cell Biol       Date:  1997-04       Impact factor: 4.272

9.  ZBP1 enhances cell polarity and reduces chemotaxis.

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10.  Actin is a surface component of calf pulmonary artery endothelial cells in culture.

Authors:  J Moroianu; J W Fett; J F Riordan; B L Vallee
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

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