Literature DB >> 1384654

Localization of the viral and cellular Src kinases to perinuclear vesicles in fibroblasts.

T Redmond1, B K Brott, R Jove, M J Welsh.   

Abstract

Previous studies have shown that the viral oncogene product, v-Src, is localized to a perinuclear structure. Here, we demonstrate by immunofluorescence analysis that the perinuclear structure corresponds to a local concentration of vesicles. Overexpressed normal cellular Src, c-Src, and a temperature-sensitive mutant of v-Src also are associated with these perinuclear vesicles. This perinuclear localization is observed in a variety of cell types using several different antibodies to Src, and it is independent of the fixation method. Immunoelectron ultracryomicroscopic analysis of rat fibroblast cells transformed by v-Src demonstrates an association of this protein with the limiting membranes of vesicles concentrated in the perinuclear region. These vesicles appear at the electron microscopic level to be multivesicular bodies on the basis of their size (0.3-1.0 microns in diameter), large electron-transparent lumens, and electron-dense vesicular inclusions. Morphometric analysis indicates that approximately 20% of the total cell v-Src protein is associated with these structures. This subpopulation of v-Src may have been recovered from the plasma membrane via the endocytotic pathway in a manner analogous to endocytosis of the epidermal growth factor receptor. Localization of the Src tyrosine kinases to these perinuclear endocytotic vesicles may be necessary for oncogenic transformation by v-Src and for normal functions of c-Src.

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Year:  1992        PMID: 1384654

Source DB:  PubMed          Journal:  Cell Growth Differ        ISSN: 1044-9523


  7 in total

1.  The src-family protein-tyrosine kinase p59hck is located on the secretory granules in human neutrophils and translocates towards the phagosome during cell activation.

Authors:  H Möhn; V Le Cabec; S Fischer; I Maridonneau-Parini
Journal:  Biochem J       Date:  1995-07-15       Impact factor: 3.857

2.  Protein kinase Calpha activates c-Src and induces podosome formation via AFAP-110.

Authors:  Amanda Gatesman; Valerie G Walker; Joseph M Baisden; Scott A Weed; Daniel C Flynn
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

Review 3.  Single-cell imaging of mechanotransduction in endothelial cells.

Authors:  Shaoying Lu; Yingxiao Wang
Journal:  Prog Mol Biol Transl Sci       Date:  2014       Impact factor: 3.622

4.  Identification of c-Src tyrosine kinase substrates in platelet-derived growth factor receptor signaling.

Authors:  Ramars Amanchy; Jun Zhong; Rosa Hong; James H Kim; Marjan Gucek; Robert N Cole; Henrik Molina; Akhilesh Pandey
Journal:  Mol Oncol       Date:  2009-07-10       Impact factor: 6.603

5.  ASAP1, a phospholipid-dependent arf GTPase-activating protein that associates with and is phosphorylated by Src.

Authors:  M T Brown; J Andrade; H Radhakrishna; J G Donaldson; J A Cooper; P A Randazzo
Journal:  Mol Cell Biol       Date:  1998-12       Impact factor: 4.272

6.  Association of the amino-terminal half of c-Src with focal adhesions alters their properties and is regulated by phosphorylation of tyrosine 527.

Authors:  K B Kaplan; K B Bibbins; J R Swedlow; M Arnaud; D O Morgan; H E Varmus
Journal:  EMBO J       Date:  1994-10-17       Impact factor: 11.598

7.  Podosomes and Invadopodia: Related structures with Common Protein Components that May Promote Breast Cancer Cellular Invasion.

Authors:  Daniel C Flynn; Youngjin Cho; Deanne Vincent; Jess M Cunnick
Journal:  Breast Cancer (Auckl)       Date:  2008-05-29
  7 in total

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