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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2023
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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 |
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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 |
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