Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, 77030, USA; Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Biochem Biophys Res Commun. 2021 Jan 1;534:864-870. doi: 10.1016/j.bbrc.2020.10.086. Epub 2020 Nov 7.
Bile acids have recently emerged as key metabolic hormones with beneficial impacts in multiple metabolic diseases. We previously discovered that hepatic bile acid overload distally modulates glucose and fatty acid metabolism in adipose tissues to exert anti-obesity effects. However, the detailed mechanisms that explain the salutary effects of serum bile acid elevation remain unclear. Here, proteomic profiling identified a new hepatokine, Orosomucoid (ORM) that governs liver-adipose tissue crosstalk. Hepatic ORMs were highly induced by both genetic and dietary bile acid overload. To address the direct metabolic effects of ORM, purified ORM proteins were administered during adipogenic differentiation of 3T3-L1 cells and mouse stromal vascular fibroblasts. ORM suppressed adipocyte differentiation and strongly inhibited gene expression of adipogenic transcription factors such as C/EBPβ, KLF5, C/EBPα, and PPARγ. Taken together, our data clearly suggest that bile acid-induced ORM secretion from the liver blocks adipocyte differentiation, potentially linked to anti-obesity effect of bile acids.
胆汁酸最近被认为是具有多种代谢疾病有益影响的关键代谢激素。我们之前发现,肝脏胆汁酸过载会在脂肪组织中远程调节葡萄糖和脂肪酸代谢,从而发挥抗肥胖作用。然而,解释血清胆汁酸升高的有益影响的详细机制仍不清楚。在这里,蛋白质组学分析鉴定了一种新的肝激素——乳白蛋白 (ORM),它控制着肝脏-脂肪组织的串扰。遗传和饮食性胆汁酸过载都会使肝脏 ORM 高度诱导。为了研究 ORM 的直接代谢作用,在 3T3-L1 细胞和小鼠基质血管成纤维细胞的脂肪生成分化过程中给予纯化的 ORM 蛋白。ORM 抑制脂肪细胞分化,并强烈抑制脂肪生成转录因子如 C/EBPβ、KLF5、C/EBPα 和 PPARγ 的基因表达。总之,我们的数据清楚地表明,肝脏分泌的胆汁酸诱导的 ORM 阻止脂肪细胞分化,这可能与胆汁酸的抗肥胖作用有关。