Literature DB >> 10644641

Expression of heat shock proteins in turtle and mammal hearts: relationship to anoxia tolerance.

J Chang1, A A Knowlton, J S Wasser.   

Abstract

Heat shock proteins (HSPs) may play a cardioprotective role during hypoxia or ischemia. We hypothesized that cardiac tissue from hypoxia-tolerant animals might have high levels of specific HSPs. We measured myocardial HSP60 and HSP72/73 in painted and softshell turtles during normoxia and anoxia (12 h) and after recovery (12 or 24 h). We also measured myocardial HSPs in normoxic rats and rabbits. During normoxia, hearts from the most highly anoxia-tolerant species, the painted turtle, expressed the highest levels of HSP60 (22.6+/-2.0 mg/g total protein) followed by softshells (11.5+/-0.8 mg/g), rabbits (6.8+/-0.9 mg/g), and rats (4.5+/-0.5 mg/g). HSP72/73 levels, however, were not significantly different. HSP60 levels in hearts from both painted and softshell turtles did not deviate significantly from control values after either 12 h of anoxia or 12 or 24 h of recovery. The pattern of changes observed in HSP72/73 was quite different in the two turtle species. In painted turtles anoxia induced a significant increase in myocardial HSP72/73 (from 2.8+/-0.1 mg/g normoxic to 3.9+/-0.2 mg/g anoxic, P<0.05). By 12 h of recovery, HSP72/73 had returned to control levels (2.7+/-0.1 mg/g) and remained there through 24 h (2.6+/-0.2 mg/g). In softshell turtles, HSP72/73 decreased significantly after 12 h of anoxia (from 2.4+/-0.4 mg/g normoxic to 1.3+/-0.2 mg/g anoxic, P<0.05). HSP72/73 levels were still slightly below control after 12 h of recovery (2.1+/-0.1 mg/g) and then rose to significantly above control after 24 h of recovery (4.1+/-0.7 mg/g, P<0.05). We also conclude that anoxia-tolerant and anoxia-sensitive turtles exhibit different patterns of myocardial HSP changes during anoxia and recovery. Whether these changes correlate with their relative degrees of anoxia tolerance remains to be determined.

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Year:  2000        PMID: 10644641     DOI: 10.1152/ajpregu.2000.278.1.R209

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  12 in total

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Journal:  Cell Stress Chaperones       Date:  2004       Impact factor: 3.667

3.  Modulation of stress proteins and apoptotic regulators in the anoxia tolerant turtle brain.

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Journal:  J Neurochem       Date:  2009-03-26       Impact factor: 5.372

4.  Regulation of the heat shock response under anoxia in the turtle, Trachemys scripta elegans.

Authors:  Anastasia Krivoruchko; Kenneth B Storey
Journal:  J Comp Physiol B       Date:  2009-10-16       Impact factor: 2.200

5.  Histone methyltransferase Setd2 is critical for the proliferation and differentiation of myoblasts.

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Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2017-01-24       Impact factor: 4.739

6.  Protein tyrosine phosphatase-like A regulates myoblast proliferation and differentiation through MyoG and the cell cycling signaling pathway.

Authors:  Xi Lin; Xiangsheng Yang; Qi Li; Yanlin Ma; Shuang Cui; Dacheng He; Xia Lin; Robert J Schwartz; Jiang Chang
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7.  Hsp72 expression enhances survival in adenosine triphosphate-depleted renal epithelial cells.

Authors:  Y H Wang; A A Knowlton; F H Li; S C Borkan
Journal:  Cell Stress Chaperones       Date:  2002-04       Impact factor: 3.667

8.  Activation of Rho-associated coiled-coil protein kinase 1 (ROCK-1) by caspase-3 cleavage plays an essential role in cardiac myocyte apoptosis.

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Review 9.  Hibernating without oxygen: physiological adaptations of the painted turtle.

Authors:  Donald C Jackson
Journal:  J Physiol       Date:  2002-09-15       Impact factor: 5.182

Review 10.  Forever young: mechanisms of natural anoxia tolerance and potential links to longevity.

Authors:  Anastasia Krivoruchko; Kenneth B Storey
Journal:  Oxid Med Cell Longev       Date:  2010 May-Jun       Impact factor: 6.543

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