Literature DB >> 9642282

Heat shock protein 72 modulates pathways of stress-induced apoptosis.

K A Buzzard1, A J Giaccia, M Killender, R L Anderson.   

Abstract

The resistance to stress-induced apoptosis conferred by the thermotolerant state or by exogenous expression of HSP72 was measured in mouse embryo fibroblasts. The induction of thermotolerance protects cells from heat, tumor necrosis factor alpha (TNFalpha), and ceramide-induced apoptosis but not from ionizing radiation. Because the development of thermotolerance is associated with increased levels of heat shock proteins, we determined whether constitutive expression of one of the major inducible heat shock proteins, HSP72, could also protect cells from stress-induced apoptosis. Cells expressing constitutive HSP72 were shown to have significantly reduced levels of apoptosis after heat, TNFalpha, and ceramide but not after ionizing radiation. Activation of stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK) was found to be strongly inhibited in thermotolerant cells after heat shock but not after other stresses. Cells that constitutively express HSP72 did not demonstrate decreased SAPK/JNK activation after any of these stresses. Thus, factors other than HSP72 that are induced in the thermotolerant state are able to reduce activation of SAPK/JNK after heat stress. Notably, the level of activation of SAPK/JNK did not correlate with the amount of apoptosis detected after different stresses. Constitutive HSP72 expression inhibited poly(ADP-ribose) polymerase cleavage in cells after heat shock and TNFalpha but not after ceramide or ionizing radiation. The results suggest either that SAPK/JNK activation is not required for apoptosis in mouse embryo fibroblasts or that HSP72 acts downstream of SAPK/JNK. Furthermore, the data support the concept that caspase activity, which can be down-regulated by HSP72, is a crucial step in stress-induced apoptosis. Based on data presented here and elsewhere, we propose that the heat shock protein family can be classified as a class of anti-apoptotic genes, in addition to the Bcl-2 and inhibitor of apoptosis protein families of genes.

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Year:  1998        PMID: 9642282     DOI: 10.1074/jbc.273.27.17147

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  58 in total

1.  Heat shock factor 1-mediated thermotolerance prevents cell death and results in G2/M cell cycle arrest.

Authors:  J C Luft; I J Benjamin; R Mestril; D J Dix
Journal:  Cell Stress Chaperones       Date:  2001-10       Impact factor: 3.667

2.  Heat shock and ceramide have different apoptotic pathways in radiation induced fibrosarcoma (RIF) cells.

Authors:  Hee-Jung Kim; Kong-Joo Lee
Journal:  Mol Cell Biochem       Date:  2002-01       Impact factor: 3.396

3.  The chaperone function of hsp70 is required for protection against stress-induced apoptosis.

Authors:  D D Mosser; A W Caron; L Bourget; A B Meriin; M Y Sherman; R I Morimoto; B Massie
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

Review 4.  Heat shock protein 70 (hsp70) as an emerging drug target.

Authors:  Christopher G Evans; Lyra Chang; Jason E Gestwicki
Journal:  J Med Chem       Date:  2010-06-24       Impact factor: 7.446

5.  Stress response of the cell to exposure to ultraweak electromagnetic radiation.

Authors:  E G Novoselova; O V Glushkova; O A Sinotova; E E Fesenko
Journal:  Dokl Biol Sci       Date:  2005 Mar-Apr

Review 6.  Antibodies against heat shock proteins in environmental stresses and diseases: friend or foe?

Authors:  Tangchun Wu; Robert M Tanguay
Journal:  Cell Stress Chaperones       Date:  2006       Impact factor: 3.667

7.  Heat shock proteins and Bcl-2 expression and function in relation to the differential hyperthermic sensitivity between leukemic and normal hematopoietic cells.

Authors:  R Setroikromo; P K Wierenga; M A W H van Waarde; J F Brunsting; E Vellenga; H H Kampinga
Journal:  Cell Stress Chaperones       Date:  2007       Impact factor: 3.667

8.  TRAIL-induced apoptosis is enhanced by heat shock protein 70 expression.

Authors:  N J Clemons; R L Anderson
Journal:  Cell Stress Chaperones       Date:  2006       Impact factor: 3.667

9.  Members of the heat-shock protein 70 family promote cancer cell growth by distinct mechanisms.

Authors:  Mikkel Rohde; Mads Daugaard; Mette Hartvig Jensen; Kristian Helin; Jesper Nylandsted; Marja Jäättelä
Journal:  Genes Dev       Date:  2005-03-01       Impact factor: 11.361

10.  Hsp72 chaperone function is dispensable for protection against stress-induced apoptosis.

Authors:  Ari M Chow; Rohan Steel; Robin L Anderson
Journal:  Cell Stress Chaperones       Date:  2008-09-26       Impact factor: 3.667

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