Literature DB >> 3170655

Enhanced constitutive expression of the 27-kDa heat shock proteins in heat-resistant variants from Chinese hamster cells.

P Chrétien1, J Landry.   

Abstract

Four heat-resistant variants were isolated after treatment of Chinese hamster lung cells with the mutagen ethyl methane sulfonate, followed by a single-step selection procedure consisting in a severe hyperthermic treatment of 4 h at 44 degrees C. The isolated clones had a stable resistant phenotype for at least 150 generations during which they showed a 5,000-fold increased survival to a 4-h treatment at 44 degrees C when compared to wild-type cells. Comparative two-dimensional electrophoretic analyses of proteins revealed that, like induced thermotolerant wild-type cells (i.e., cells induced to a transient physiological state of thermotolerance by a sublethal heat conditioning treatment administered 18 h before), the heat-resistant variants had, at normal temperature, an increased content of a heat-shock protein with Mr of 27,000 (HSP27). In three of the four heat-resistant variants, the increased content of HSP27 was correlated with a two-fold increase in the constitutive level of the mRNA encoding HSP27. Chinese hamster HSP27 is composed of three species that differ in their relative isoelectric point, among which the two most acidic forms are phosphoproteins. In both the heat-resistant variant and wild-type cells, heat shock induces a rapid enhancement of the phosphorylation of HSP27: maximal phosphorylation occurs within 10 min upon changing the incubation temperature from 35 degrees to 44 degrees C. A concomitant shift in silver-staining intensity is rapidly detectable between the three isoforms, which seems to indicate that the two phosphorylated species represent post-translational modifications of the more basic species. It is concluded that most likely the enhanced expression of HSP27 is linked to the resistant phenotype of the variants. The study provides supporting evidence that both the content and phosphorylation status of HSP27 are determining factors in the ability of cells to survive hyperthermic treatments.

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Year:  1988        PMID: 3170655     DOI: 10.1002/jcp.1041370119

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  22 in total

1.  Stress protection by a fluorescent Hsp27 chimera that is independent of nuclear translocation or multimeric dissociation.

Authors:  Michael J Borrelli; Laura J Bernock; Jacques Landry; Douglas R Spitz; Lee A Weber; Eileen Hickey; Michael L Freeman; Peter M Corry
Journal:  Cell Stress Chaperones       Date:  2002-07       Impact factor: 3.667

2.  Induction of a chicken small heat shock (stress) protein: evidence of multilevel posttranscriptional regulation.

Authors:  B V Edington; L E Hightower
Journal:  Mol Cell Biol       Date:  1990-09       Impact factor: 4.272

Review 3.  Heat shock protein 27: its potential role in vascular disease.

Authors:  Gordon Ferns; Sedigheh Shams; Shahida Shafi
Journal:  Int J Exp Pathol       Date:  2006-08       Impact factor: 1.925

4.  Vascular heat shock protein expression in response to stress. Endocrine and autonomic regulation of this age-dependent response.

Authors:  R Udelsman; M J Blake; C A Stagg; D G Li; D J Putney; N J Holbrook
Journal:  J Clin Invest       Date:  1993-02       Impact factor: 14.808

5.  Expression of inducible Hsp70 enhances the proliferation of MCF-7 breast cancer cells and protects against the cytotoxic effects of hyperthermia.

Authors:  J A Barnes; D J Dix; B W Collins; C Luft; J W Allen
Journal:  Cell Stress Chaperones       Date:  2001-10       Impact factor: 3.667

Review 6.  Activation of the mitogen-activated protein kinase pathways by heat shock.

Authors:  Sonia Dorion; Jacques Landry
Journal:  Cell Stress Chaperones       Date:  2002-04       Impact factor: 3.667

7.  The role of the cysteine residue in the chaperone and anti-apoptotic functions of human Hsp27.

Authors:  Nagarekha Pasupuleti; Mahesha Gangadhariah; Smitha Padmanabha; Puttur Santhoshkumar; Ram H Nagaraj
Journal:  J Cell Biochem       Date:  2010-05-15       Impact factor: 4.429

8.  Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy.

Authors:  Leonardo Almeida-Souza; Sofie Goethals; Vicky de Winter; Ines Dierick; Rodrigo Gallardo; Joost Van Durme; Joy Irobi; Jan Gettemans; Frederic Rousseau; Joost Schymkowitz; Vincent Timmerman; Sophie Janssens
Journal:  J Biol Chem       Date:  2010-02-23       Impact factor: 5.157

9.  Mammalian stress proteins HSP70 and HSP28 coinduced by nicotine and either ethanol or heat.

Authors:  G M Hahn; E C Shiu; E A Auger
Journal:  Mol Cell Biol       Date:  1991-12       Impact factor: 4.272

10.  Rapid increase in pH set-point of the Na(+)-in-dependent chloride/bicarbonate antiporter in Vero cells exposed to heat shock.

Authors:  J Ludt; K Sandvig; S Olsnes
Journal:  J Membr Biol       Date:  1993-06       Impact factor: 1.843

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