Cargando…

Gut microbes and the liver circadian clock partition glucose and lipid metabolism

Circadian rhythms govern glucose homeostasis, and their dysregulation leads to complex metabolic diseases. Gut microbes exhibit diurnal rhythms that influence host circadian networks and metabolic processes, yet underlying mechanisms remain elusive. Here, we showed hierarchical, bidirectional commun...

Descripción completa

Detalles Bibliográficos
Autores principales: Frazier, Katya, Manzoor, Sumeed, Carroll, Katherine, DeLeon, Orlando, Miyoshi, Sawako, Miyoshi, Jun, St. George, Marissa, Tan, Alan, Chrisler, Evan A., Izumo, Mariko, Takahashi, Joseph S., Rao, Mrinalini C., Leone, Vanessa A., Chang, Eugene B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503806/
https://www.ncbi.nlm.nih.gov/pubmed/37712426
http://dx.doi.org/10.1172/JCI162515
_version_ 1785106601229680640
author Frazier, Katya
Manzoor, Sumeed
Carroll, Katherine
DeLeon, Orlando
Miyoshi, Sawako
Miyoshi, Jun
St. George, Marissa
Tan, Alan
Chrisler, Evan A.
Izumo, Mariko
Takahashi, Joseph S.
Rao, Mrinalini C.
Leone, Vanessa A.
Chang, Eugene B.
author_facet Frazier, Katya
Manzoor, Sumeed
Carroll, Katherine
DeLeon, Orlando
Miyoshi, Sawako
Miyoshi, Jun
St. George, Marissa
Tan, Alan
Chrisler, Evan A.
Izumo, Mariko
Takahashi, Joseph S.
Rao, Mrinalini C.
Leone, Vanessa A.
Chang, Eugene B.
author_sort Frazier, Katya
collection PubMed
description Circadian rhythms govern glucose homeostasis, and their dysregulation leads to complex metabolic diseases. Gut microbes exhibit diurnal rhythms that influence host circadian networks and metabolic processes, yet underlying mechanisms remain elusive. Here, we showed hierarchical, bidirectional communication among the liver circadian clock, gut microbes, and glucose homeostasis in mice. To assess this relationship, we utilized mice with liver-specific deletion of the core circadian clock gene Bmal1 via Albumin-cre maintained in either conventional or germ-free housing conditions. The liver clock, but not the forebrain clock, required gut microbes to drive glucose clearance and gluconeogenesis. Liver clock dysfunctionality expanded proportions and abundances of oscillating microbial features by 2-fold relative to that in controls. The liver clock was the primary driver of differential and rhythmic hepatic expression of glucose and fatty acid metabolic pathways. Absent the liver clock, gut microbes provided secondary cues that dampened these rhythms, resulting in reduced lipid fuel utilization relative to carbohydrates. All together, the liver clock transduced signals from gut microbes that were necessary for regulating glucose and lipid metabolism and meeting energy demands over 24 hours.
format Online
Article
Text
id pubmed-10503806
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society for Clinical Investigation
record_format MEDLINE/PubMed
spelling pubmed-105038062023-09-16 Gut microbes and the liver circadian clock partition glucose and lipid metabolism Frazier, Katya Manzoor, Sumeed Carroll, Katherine DeLeon, Orlando Miyoshi, Sawako Miyoshi, Jun St. George, Marissa Tan, Alan Chrisler, Evan A. Izumo, Mariko Takahashi, Joseph S. Rao, Mrinalini C. Leone, Vanessa A. Chang, Eugene B. J Clin Invest Research Article Circadian rhythms govern glucose homeostasis, and their dysregulation leads to complex metabolic diseases. Gut microbes exhibit diurnal rhythms that influence host circadian networks and metabolic processes, yet underlying mechanisms remain elusive. Here, we showed hierarchical, bidirectional communication among the liver circadian clock, gut microbes, and glucose homeostasis in mice. To assess this relationship, we utilized mice with liver-specific deletion of the core circadian clock gene Bmal1 via Albumin-cre maintained in either conventional or germ-free housing conditions. The liver clock, but not the forebrain clock, required gut microbes to drive glucose clearance and gluconeogenesis. Liver clock dysfunctionality expanded proportions and abundances of oscillating microbial features by 2-fold relative to that in controls. The liver clock was the primary driver of differential and rhythmic hepatic expression of glucose and fatty acid metabolic pathways. Absent the liver clock, gut microbes provided secondary cues that dampened these rhythms, resulting in reduced lipid fuel utilization relative to carbohydrates. All together, the liver clock transduced signals from gut microbes that were necessary for regulating glucose and lipid metabolism and meeting energy demands over 24 hours. American Society for Clinical Investigation 2023-09-15 /pmc/articles/PMC10503806/ /pubmed/37712426 http://dx.doi.org/10.1172/JCI162515 Text en © 2023 Frazier et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Frazier, Katya
Manzoor, Sumeed
Carroll, Katherine
DeLeon, Orlando
Miyoshi, Sawako
Miyoshi, Jun
St. George, Marissa
Tan, Alan
Chrisler, Evan A.
Izumo, Mariko
Takahashi, Joseph S.
Rao, Mrinalini C.
Leone, Vanessa A.
Chang, Eugene B.
Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title_full Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title_fullStr Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title_full_unstemmed Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title_short Gut microbes and the liver circadian clock partition glucose and lipid metabolism
title_sort gut microbes and the liver circadian clock partition glucose and lipid metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503806/
https://www.ncbi.nlm.nih.gov/pubmed/37712426
http://dx.doi.org/10.1172/JCI162515
work_keys_str_mv AT frazierkatya gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT manzoorsumeed gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT carrollkatherine gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT deleonorlando gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT miyoshisawako gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT miyoshijun gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT stgeorgemarissa gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT tanalan gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT chrislerevana gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT izumomariko gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT takahashijosephs gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT raomrinalinic gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT leonevanessaa gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism
AT changeugeneb gutmicrobesandthelivercircadianclockpartitionglucoseandlipidmetabolism