Hepatocyte SREBP signaling mediates clock communication within the liver.

Abstract

Rhythmic intraorgan communication coordinates environmental signals and the cell-intrinsic clock to maintain organ homeostasis. Hepatocyte-specific KO of core components of the molecular clock Rev-erbα and -β (Reverb-hDKO) alters cholesterol and lipid metabolism in hepatocytes as well as rhythmic gene expression in nonparenchymal cells (NPCs) of the liver. Here, we report that in fatty liver caused by diet-induced obesity (DIO), hepatocyte SREBP cleavage-activating protein (SCAP) was required for Reverb-hDKO-induced diurnal rhythmic remodeling and epigenomic reprogramming in liver macrophages (LMs). Integrative analyses of isolated hepatocytes and LMs revealed that SCAP-dependent lipidomic changes in REV-ERB-depleted hepatocytes led to the enhancement of LM metabolic rhythms. Hepatocytic loss of REV-ERBα and β (REV-ERBs) also attenuated LM rhythms via SCAP-independent polypeptide secretion. These results shed light on the signaling mechanisms by which hepatocytes regulate diurnal rhythms in NPCs in fatty liver disease caused by DIO.

• Authors: Dongyin Guan, Hosung Bae, Dishu Zhou, Ying Chen, Chunjie Jiang, Cam Mong La, Yang Xiao, Kun Zhu, Wenxiang Hu, Trang Minh Trinh, Panpan Liu, Ying Xiong, Bishuang Cai, Cholsoon Jang, Mitchell A Lazar
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 133 Issue 8 (04 17 2023) ISSN: 1558-8238 [Electronic] United States
• PMID: 37066875 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Sterol Regulatory Element Binding Protein 1
• Nuclear Receptor Subfamily 1, Group D, Member 1

Topics

• Sterol Regulatory Element Binding Protein 1 (metabolism)
• Nuclear Receptor Subfamily 1, Group D, Member 1 (genetics, metabolism)
• Liver (metabolism)
• Hepatocytes (metabolism)
• Circadian Rhythm (physiology)
• Communication