Heat Shock Proteins and Cytoprotection: Atp-Deprived Mammalian Cells

by Alexander E. Kabakov, Vladimir L. Gabai

Overview

This book considers a recently discovered function of heat shock proteins (HSP): adaptation of mammalian cells to energy deficiency. It discusses the following main problems: 1) how do cells sense transient ATP decrease and why does it evoke heat shock response?; 2) how can HSPs protect cells from damage and death and what are their intracellular targets?; 3) what may be a clinical application of HSP-mediated adaptation to ischemia?

Product Details

ISBN-13:	9780412132315
Publisher:	Springer US
Publication date:	03/15/1997
Series:	Molecular Biology Intelligence Unit
Edition description:	1997
Pages:	237
Product dimensions:	7.01(w) x 10.00(h) x 0.28(d)

Table of Contents

1. Heat Shock Proteins and the Regulation of Heat Shock Gene Expression in Eukaryotes.- 1.1. The Family of Stress Proteins and Molecular Chaperones.- 1.2. The Regulation of Heat Shock Gene Expression in Eukaryotes.- Concluding Remarks.- 2. ATP Homeostasis, Ionic Balance and Cell Viability.- 2.1. ATP Homeostasis in Mammalian Cells.- 2.2. Cell Viability and ATP Depletion.- 2.3. Significance of Ionic Imbalance for the Death of ATP-Depleted Cells.- 2.4. Mihondrial Dysfunction and Damage During Ischemia.- Concluding Remarks.- 3. “Proteotoxicity” of ATP Depletion: Disruption of the Cytoskeleton, Protein Aggregation and Involvement of Molecular Chaperones.- 3.1. The Cytoskeleton Under ATP Deprivation.- 3.2. Protein Aggregation in Energy-Deprived Cells.- 3.3. How Do Heat Shock Proteins Respond to ATP Depletion?.- Concluding Remarks.- 4. ATP Depletion as Inducer of Heat Shock Protein Expression.- 4.1. Anoxia and Mihondrial Inhibitors Activate HSP Gene Expression.- 4.2. Ischemia-Induced HSP Synthesis in the Heart.- 4.3. Stress Protein Expression in Post-Ischemic Brain.- 4.4. Ischemia-Induced Stress Protein Synthesis in Other Normal Tissues and Tumor Cells.- 4.5. Possible Mechanisms of HSP Accumulation After ATP Depletion.- Concluding Remarks.- 5. Heat Shock Proteins and Cardioresistance to Ischemia.- 5.1. Heat Shock-Induced Cardioresistance to Ischemia/Reperfusion Injury.- 5.2. The Role of Myocardial HSPs in Ischemie Preconditioning.- 5.3. The Cardioresistance Induced by Other Stimuli Can Also Be Associated with HSPs.- 5.4. Evidence for the Involvement of HSP70 in Cardioprotection.- 5.5. Are Other Stress Proteins Cardioprotective?.- Concluding Remarks.- 6. Involvement of Heat Shock Proteins in Protection of Various Normal and Tumor Cells from Ischemic Insult.- 6.1. HSPsand Ischemic Tolerance in the Brain.- 6.2. Ischemic Tolerance in the Kidney.- 6.3. HSPs and Protection from Ischemia of Other Organs and Tissues.- 6.4..- Concluding Remarks.- 7. What Are the Mechanisms of Heat Shock Protein-Mediated Cytoprotection Under ATP Deprivation?.- 7.1. Two Paradigms of Cell Tolerance to ATP Deprivation: Reduced Injury During the Stress and the Improved Post-Stress Recovery.- 7.2. Chaperoning Under ATP Depletion as a Special Function of HSP70.- 7.3. How Other Stress Proteins Might Maintain the Viability of ATP-Deprived Cells.- 7.4. How Do HSPs Protect Cells against Necrosis during ATP Depletion?.- 8. Mechanisms of Heat Shock Protein-Mediated Protection from Ischemia-Induced Apoptosis.- 8.1. HSPs and Triggering of Apoptosis in Ischemic Cells.- 8.2. HSPs and Transduction of the Apoptotic Signal.- 8.3. HSPs and the Execution of Apoptosis.- 9. Conclusions and Perspectives.- 9.1. Adaptation to Energy Starvation on The Molecular Level.- 9.2. Heat Shock Proteins and Ischemia: Significance for Medicine.- Concluding Remarks.

Editorial Reviews

Reviews the studies on the role of cell energetics in the mechanism of the stress response inductions, presenting a selection of facts, speculations, and hypotheses concerning the involvement of heat-shock proteins in protecting the cell during depletion of the nucleotide ATP, which supplies energy to the cell. Among the topics are the regulation of heat-shock gene expression in eukaryotes, ATP depletion as an inducer of heat-shock protein expression, protecting various normal and tumor cells from ischemic insult, and mechanisms of protection from ischemia-induced apoptosis. Annotation c. by Book News, Inc., Portland, Or.

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