The Hepatokine Orosomucoid 2 Mediates Beneficial Metabolic Effects of Bile Acids

Author:

Lee Sung Ho12,Suh Ji Ho3,Heo Mi Jeong3,Choi Jong Min4,Yang Yang3,Jung Hyun-Jung3,Gao Zhanguo5,Yu Yongmei5,Jung Sung Yun6,Kolonin Mikhail G.5ORCID,Cox Aaron R.5,Hartig Sean M.17ORCID,Eltzschig Holger K.3,Ju Cynthia3,Moore David D.18,Kim Kang Ho13ORCID

Affiliation:

1. 1Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX

2. 2College of Pharmacy and Research Institute of Pharmaceutical Sciences, Chonnam National University, Gwangju, Korea

3. 3Department of Anesthesiology, Critical Care and Pain Medicine and Center for Perioperative Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX

4. 4Systems Onco-Immunology Laboratory, David J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX

5. 5The Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX

6. 6Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX

7. 7Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Baylor College of Medicine, Houston, TX

8. 8Department of Nutritional Sciences and Toxicology, University of California, Berkeley, Berkeley, CA

Abstract

Bile acids (BAs) are pleiotropic regulators of metabolism. Elevated levels of hepatic and circulating BAs improve energy metabolism in peripheral organs, but the precise mechanisms underlying the metabolic benefits and harm still need to be fully understood. In the current study, we identified orosomucoid 2 (ORM2) as a liver-secreted hormone (i.e., hepatokine) induced by BAs and investigated its role in BA-induced metabolic improvements in mouse models of diet-induced obesity. Contrary to our expectation, under a high-fat diet (HFD), our Orm2 knockout (Orm2-KO) exhibited a lean phenotype compared with C57BL/6J control, partly due to the increased energy expenditure. However, when challenged with a HFD supplemented with cholic acid, Orm2-KO eliminated the antiobesity effect of BAs, indicating that ORM2 governs BA-induced metabolic improvements. Moreover, hepatic ORM2 overexpression partially replicated BA effects by enhancing insulin sensitivity. Mechanistically, ORM2 suppressed interferon-γ/STAT1 activities in inguinal white adipose tissue depots, forming the basis for anti-inflammatory effects of BAs and improving glucose homeostasis. In conclusion, our study provides new insights into the molecular mechanisms of BA-induced liver-adipose cross talk through ORM2 induction. Article Highlights

Funder

National Heart, Lung, and Blood Institute

American Heart Association

Baylor College of Medicine

DOD

Division of Diabetes, Endocrinology, and Metabolic Diseases

National Cancer Institute

Bovay Foundation and the Levy-Longenbaugh Fund

Publisher

American Diabetes Association

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