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PMID: 20965422 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Autophagy and the integrated stress response.

Molecular cell ·Vol. 40 ·No. 2 ·2010-10-22 ·Pages 280-93

Kroemer G, Mariño G, Levine B

Abstract

Autophagy is a tightly regulated pathway involving the lysosomal degradation of cytoplasmic organelles or cytosolic components. This pathway can be stimulated by multiple forms of cellular stress, including nutrient or growth factor deprivation, hypoxia, reactive oxygen species, DNA damage, protein aggregates, damaged organelles, or intracellular pathogens. Both specific, stimulus-dependent and more general, stimulus-independent signaling pathways are activated to coordinate different phases of autophagy. Autophagy can be integrated with other cellular stress responses through parallel stimulation of autophagy and other stress responses by specific stress stimuli, through dual regulation of autophagy and other stress responses by multifunctional stress signaling molecules, and/or through mutual control of autophagy and other stress responses. Thus, autophagy is a cell biological process that is a central component of the integrated stress response.

MeSH Terms
Animals Apoptosis/physiology Autophagy/physiology Cell Proliferation Cellular Senescence/physiology Humans Lysosomes/metabolism Models, Biological Signal Transduction/physiology Stress, Physiological/physiology
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kroemer Guido
INSERM, U848, 39 rue Calmette Desmoulins, 94805 Villejuif, France. [email protected]
Mariño Guillermo
Levine Beth
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Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-4164
Published
2010-10-22
Pages
280-93
Language
English
Region
United States
NLM ID
9802571
PMCID
PMC3127250
Subset
IM
Grants
NCI NIH HHS · R01 CA084254-10S1 · United States
NCI NIH HHS · R01 CA084254-10 · United States
NCI NIH HHS · R01 CA084254 · United States
NIAID NIH HHS · R01 AI051367-06 · United States
Howard Hughes Medical Institute · United States
NIAID NIH HHS · R01 AI051367 · United States
NCI NIH HHS · R01 CA109618 · United States
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