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胆酸介导体脂联素 2 介导有益的代谢作用。

The Hepatokine Orosomucoid 2 Mediates Beneficial Metabolic Effects of Bile Acids.

机构信息

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

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

出版信息

Diabetes. 2024 May 1;73(5):701-712. doi: 10.2337/db23-0520.

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.

摘要

胆汁酸(BAs)是代谢的多效调节因子。肝内和循环胆汁酸水平的升高可改善外周器官的能量代谢,但代谢益处和危害的确切机制仍需充分理解。在本研究中,我们鉴定出结合珠蛋白 2(ORM2)是一种由 BAs 诱导的肝脏分泌的激素(即肝激素),并研究了其在 BA 诱导的肥胖症小鼠模型代谢改善中的作用。出乎意料的是,在高脂肪饮食(HFD)下,与 C57BL/6J 对照相比,我们的 Orm2 敲除(Orm2-KO)小鼠表现出瘦表型,部分原因是能量消耗增加。然而,当用补充胆酸的 HFD 进行挑战时,Orm2-KO 消除了 BAs 的抗肥胖作用,表明 ORM2 控制着 BA 诱导的代谢改善。此外,肝脏 ORM2 的过表达部分通过增强胰岛素敏感性复制了 BA 的作用。从机制上讲,ORM2 抑制了腹股沟白色脂肪组织库中的干扰素-γ/STAT1 活性,为 BAs 的抗炎作用和改善葡萄糖稳态奠定了基础。总之,我们的研究通过 ORM2 诱导为 BA 诱导的肝脏-脂肪细胞串扰的分子机制提供了新的见解。

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