TY - JOUR
T1 - In Vivo Single-Cell Detection of Metabolic Oscillations in Stem Cells
AU - Stringari, Chiara
AU - Wang, Hong
AU - Geyfman, Mikhail
AU - Crosignani, Viera
AU - Kumar, Vivek
AU - Takahashi, Joseph S.
AU - Andersen, Bogi
AU - Gratton, Enrico
N1 - Funding Information:
Work was supported with NIH grants R01 AR056439, P50 GM076516, and P41 GM103540.
Publisher Copyright:
© 2015 The Authors.
PY - 2015/1/6
Y1 - 2015/1/6
N2 - Through the use of bulk measurements in metabolic organs, the circadian clock was shown to play roles in organismal energy homeostasis. However, the relationship between metabolic and circadian oscillations has not been studied invivo at a single-cell level. Also, it is unknown whether the circadian clock controls metabolism in stem cells. We used a sensitive, noninvasive method to detect metabolic oscillations and circadian phase within epidermal stem cells in live mice at the single-cell level. We observe a higher NADH/NAD+ ratio, reflecting an increased glycolysis/oxidative phosphorylation ratio during the night compared to the day. Furthermore, we demonstrate that single-cell metabolic heterogeneity within the basal cell layer correlates with the circadian clock and that diurnal fluctuations in NADH/NAD+ ratio are Bmal1 dependent. Our data show that, in proliferating stem cells, the circadian clock coordinates activities of oxidative phosphorylation and glycolysis with DNA synthesis, perhaps as a protective mechanism against genotoxicity.
AB - Through the use of bulk measurements in metabolic organs, the circadian clock was shown to play roles in organismal energy homeostasis. However, the relationship between metabolic and circadian oscillations has not been studied invivo at a single-cell level. Also, it is unknown whether the circadian clock controls metabolism in stem cells. We used a sensitive, noninvasive method to detect metabolic oscillations and circadian phase within epidermal stem cells in live mice at the single-cell level. We observe a higher NADH/NAD+ ratio, reflecting an increased glycolysis/oxidative phosphorylation ratio during the night compared to the day. Furthermore, we demonstrate that single-cell metabolic heterogeneity within the basal cell layer correlates with the circadian clock and that diurnal fluctuations in NADH/NAD+ ratio are Bmal1 dependent. Our data show that, in proliferating stem cells, the circadian clock coordinates activities of oxidative phosphorylation and glycolysis with DNA synthesis, perhaps as a protective mechanism against genotoxicity.
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U2 - 10.1016/j.celrep.2014.12.007
DO - 10.1016/j.celrep.2014.12.007
M3 - Article
C2 - 25543138
AN - SCOPUS:84920864502
SN - 2211-1247
VL - 10
SP - 1
EP - 7
JO - Cell Reports
JF - Cell Reports
IS - 1
ER -