Published September 15, 2023 | Version v1
Journal article Open

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

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.

Data availability

16S rRNA sequences are available for download at the NCBI Sequence Read Archive (accession PRJNA815335). RNA sequences are available for download at the NCBI Gene Expression Omnibus (accession GSE184303).

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Additional details

Identifiers

DOI
10.1172/JCI162515
Other
oai:uchicago.tind.io:8048

Funding

National Institute of Diabetes and Digestive and Kidney Diseases
R01DK115221
National Institute of Diabetes and Digestive and Kidney Diseases
P30DK42086
National Institute of Diabetes and Digestive and Kidney Diseases
K01DK111785
National Institute of Diabetes and Digestive and Kidney Diseases
F31DK122714
National Institute of Diabetes and Digestive and Kidney Diseases
T32DK070774
University of Chicago
GI Research Foundation

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Medicine, Molecular Metabolism and Nutrition