Department of Cell Biology, Harvard Medical School, Boston, United States; Department of Neurobiology, Harvard Medical School, Boston, United States; Department of Pathology, Brigham and Women’s Hospital, Boston, United States
Carolyn Teragawa
Department of Molecular and Cellular Biology, University of California, Davis, United States
Nont Kosaisawe
Department of Molecular and Cellular Biology, University of California, Davis, United States
Taryn E Gillies
Department of Molecular and Cellular Biology, University of California, Davis, United States
Michael Pargett
Department of Molecular and Cellular Biology, University of California, Davis, United States
Marta Minguet
Department of Molecular and Cellular Biology, University of California, Davis, United States
Kevin Distor
Department of Molecular and Cellular Biology, University of California, Davis, United States
Briana L Rocha-Gregg
Department of Molecular and Cellular Biology, University of California, Davis, United States
Jonathan L Coloff
Department of Cell Biology, Harvard Medical School, Boston, United States
Mark A Keibler
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, United States
Gregory Stephanopoulos
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, United States
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.