Autophagy is an evolutionarily conserved intracellular catabolic system. During Caenorhabditis elegans development, autophagy plays an important role in many physiological processes, including survival under starvation conditions, modulation of life span, and regulation of necrotic cell death caused by toxic ion-channel variants. Recently, it has been demonstrated that during embryogenesis, basal levels of autophagy selectively remove a group of proteins in somatic cells, including the aggregate-prone components of germline P granules. Degradation of these protein aggregates provides a genetic model to identify essential autophagy components and also to elucidate how the autophagic machinery selectively recognizes and degrades specific targets during animal development. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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Department of Anatomy, Cell and Developmental Biology, Eotvos Lorand UniversityDepartment of Anatomy, Cell and Developmental Biology, Eotvos Lorand University
机构:
Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio
Department of Cell Systems and Anatomy, University of Texas Health San Antonio
Department of Molecular Medicine, University of Texas Health SanBarshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio
SuHyuk Ko
Lizhen Chen
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Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio
Department of Cell Systems and Anatomy, University of Texas Health San Antonio
Department of Molecular Medicine, University of Texas Health SanBarshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio
机构:
Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Leboutet, Romane
Largeau, Celine
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Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Largeau, Celine
Mueller, Leonie
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Univ Cologne, Inst Genet & Cologne Excellence Cluster Cellular S, Cologne, GermanyUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Mueller, Leonie
Prigent, Magali
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Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Prigent, Magali
Quinet, Gregoire
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CNRS, Lab Chim Coordinat LCC, Toulouse, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Quinet, Gregoire
Rodriguez, Manuel S.
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CNRS, Lab Chim Coordinat LCC, Toulouse, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Rodriguez, Manuel S.
Cuif, Marie-Helene
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Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Cuif, Marie-Helene
Hoppe, Thorsten
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Univ Cologne, Inst Genet & Cologne Excellence Cluster Cellular S, Cologne, Germany
Univ Hosp Cologne, Fac Med, Ctr Mol Med Cologne CMMC, Cologne, GermanyUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Hoppe, Thorsten
Culetto, Emmanuel
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Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Culetto, Emmanuel
Lefebvre, Christophe
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Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
INSERM, U1280, Gif Sur Yvette, FranceUniv Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France
Lefebvre, Christophe
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Legouis, Renaud
Zhang, Hong
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机构:Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, Gif Sur Yvette, France