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Akt regulation of glycolysis mediates bioenergetic stability in epithelial cells.
Hung, Yin P; Teragawa, Carolyn; Kosaisawe, Nont; Gillies, Taryn E; Pargett, Michael; Minguet, Marta; Distor, Kevin; Rocha-Gregg, Briana L; Coloff, Jonathan L; Keibler, Mark A; Stephanopoulos, Gregory; Yellen, Gary; Brugge, Joan S; Albeck, John G.
Afiliação
  • Hung YP; Department of Cell Biology, Harvard Medical School, Boston, United States.
  • Teragawa C; Department of Neurobiology, Harvard Medical School, Boston, United States.
  • Kosaisawe N; Department of Pathology, Brigham and Women's Hospital, Boston, United States.
  • Gillies TE; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Pargett M; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Minguet M; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Distor K; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Rocha-Gregg BL; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Coloff JL; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Keibler MA; Department of Molecular and Cellular Biology, University of California, Davis, United States.
  • Stephanopoulos G; Department of Cell Biology, Harvard Medical School, Boston, United States.
  • Yellen G; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, United States.
  • Brugge JS; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, United States.
  • Albeck JG; Department of Neurobiology, Harvard Medical School, Boston, United States.
Elife ; 62017 12 14.
Article em En | MEDLINE | ID: mdl-29239720
ABSTRACT
Cells use multiple feedback controls to regulate metabolism in response to nutrient and signaling inputs. However, feedback creates the potential for unstable network responses. We examined how concentrations of key metabolites and signaling pathways interact to maintain homeostasis in proliferating human cells, using fluorescent reporters for AMPK activity, Akt activity, and cytosolic NADH/NAD+ redox. Across various conditions, including glycolytic or mitochondrial inhibition or cell proliferation, we observed distinct patterns of AMPK activity, including both stable adaptation and highly dynamic behaviors such as periodic oscillations and irregular fluctuations that indicate a failure to reach a steady state. Fluctuations in AMPK activity, Akt activity, and cytosolic NADH/NAD+ redox state were temporally linked in individual cells adapting to metabolic perturbations. By monitoring single-cell dynamics in each of these contexts, we identified PI3K/Akt regulation of glycolysis as a multifaceted modulator of single-cell metabolic dynamics that is required to maintain metabolic stability in proliferating cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Fosfatidilinositol 3-Quinases / Metabolismo Energético / Células Epiteliais / Proteínas Proto-Oncogênicas c-akt / Glicólise Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Fosfatidilinositol 3-Quinases / Metabolismo Energético / Células Epiteliais / Proteínas Proto-Oncogênicas c-akt / Glicólise Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos