TY - JOUR
T1 - Autophagy and the Integrated Stress Response
AU - Kroemer, Guido
AU - Mariño, Guillermo
AU - Levine, Beth
N1 - Funding Information:
G.K. is supported by the Ligue Nationale contre le Cancer (Equipes labellisée), Agence Nationale pour la Recherche (ANR), European Commission (Apo-Sys, ChemoRes), Fondation pour la Recherche Médicale (FRM), Institut National du Cancer (INCa), and Cancéropôle Ile-de-France and AXA Chair for Longevity Research. G.M. is supported by EMBO. B.L. is supported by the National Institutes of Health (NIH), National Cancer Institute (NCI)/National Institute of Allergy and Infectious Diseases (NIAID), and the Howard Hughes Medical Institute (HHMI).
PY - 2010/10/1
Y1 - 2010/10/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=78649338141&partnerID=8YFLogxK
U2 - 10.1016/j.molcel.2010.09.023
DO - 10.1016/j.molcel.2010.09.023
M3 - Review article
C2 - 20965422
AN - SCOPUS:78649338141
SN - 1097-2765
VL - 40
SP - 280
EP - 293
JO - Molecular Cell
JF - Molecular Cell
IS - 2
ER -