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药物激活的CAR/Nr1i3的结合改变肝脏中的代谢调节。

Binding of Drug-Activated CAR/Nr1i3 Alters Metabolic Regulation in the Liver.

作者信息

Tian Jianmin, Marino Rebecca, Johnson Carla, Locker Joseph

机构信息

Department of Pathology, School of Medicine, University of Pittsburgh, 200 Lothrop St, Pittsburgh, PA 15261, USA.

Department of Pathology, School of Medicine, University of Pittsburgh, 200 Lothrop St, Pittsburgh, PA 15261, USA.

出版信息

iScience. 2018 Nov 30;9:209-228. doi: 10.1016/j.isci.2018.10.018. Epub 2018 Oct 22.

Abstract

The constitutive androstane receptor (CAR/Nr1i3) regulates detoxification of drugs and other xenobiotics by the liver. Binding of these compounds, activating ligands, causes CAR to translocate to the nucleus and stimulate genes of detoxification. However, CAR activation also changes metabolism and induces rapid liver growth. To explain this gene regulation, we characterized the genome-wide early binding of CAR; its binding partner, RXRα; and the acetylation that they induced on H4K5. CAR-linked genes showed either stimulation or inhibition and regulated lipid, carbohydrate, and energy metabolism, as well as detoxification. Stimulation of expression increased, but inhibition did not decrease, H4K5Ac. Transcriptional inhibition occurred when CAR bound with HNF4α, PPARα, or FXR on the same enhancers. Functional competition among these bound nuclear receptors normally coordinates transcriptional resources as metabolism shifts. However, binding of drug-activated CAR to the same enhancers adds a new competitor that constitutively alters the normal balance of metabolic gene regulation.

摘要

组成型雄烷受体(CAR/Nr1i3)调节肝脏对药物及其他外源性物质的解毒作用。这些化合物(即激活配体)的结合会使CAR转位至细胞核并刺激解毒基因。然而,CAR激活也会改变代谢并诱导肝脏快速生长。为解释这种基因调控,我们对CAR在全基因组范围内的早期结合情况、其结合伴侣RXRα以及它们在H4K5上诱导的乙酰化进行了表征。与CAR相关的基因表现出刺激或抑制作用,并调节脂质、碳水化合物和能量代谢以及解毒作用。表达的刺激会增加H4K5Ac,但抑制不会使其减少。当CAR与HNF4α、PPARα或FXR在相同增强子上结合时,会发生转录抑制。随着代谢变化,这些结合的核受体之间的功能竞争通常会协调转录资源。然而,药物激活的CAR与相同增强子的结合增加了一个新的竞争者,从而持续改变代谢基因调控的正常平衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c9e/6222290/a1b8c4296702/fx1.jpg

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