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汽车,驶向未来。

CAR, driving into the future.

作者信息

Swales Karen, Negishi Masahiko

机构信息

Pharmacogenetics Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.

出版信息

Mol Endocrinol. 2004 Jul;18(7):1589-98. doi: 10.1210/me.2003-0397. Epub 2004 Feb 26.

Abstract

The nuclear orphan receptor CAR is active in the absence of ligand with the unique capability to be further regulated by activators. A number of these activators, including phenobarbital, do not directly bind to the receptor. Considered a xenobiotic sensing receptor, CAR transcriptionally modifies the expression of genes involved in the metabolism and elimination of xenobiotics and steroids in response to these compounds and other cellular metabolites. Its hepatic expression pattern endows the liver with the ability to protect against not only exogenous but also endogenous insults. The mechanism of CAR activation is complex, involving translocation from the cytoplasm to the nucleus in the presence of activators, followed by further activation steps in the nucleus. Although this mechanism remains under investigation, we have summarized here the cellular signaling pathways elucidated so far and speculate on the mechanism by which CAR activators regulate gene expression through this network.

摘要

核孤儿受体CAR在没有配体的情况下具有活性,具有被激活剂进一步调节的独特能力。许多这些激活剂,包括苯巴比妥,并不直接与受体结合。CAR被认为是一种外源性物质感应受体,它会根据这些化合物和其他细胞代谢物转录性地改变参与外源性物质和类固醇代谢及消除的基因的表达。其肝脏表达模式赋予肝脏不仅能抵御外源性,还能抵御内源性损伤的能力。CAR的激活机制很复杂,包括在激活剂存在的情况下从细胞质转运到细胞核,随后在细胞核中进行进一步的激活步骤。尽管这一机制仍在研究中,但我们在此总结了迄今为止阐明的细胞信号通路,并推测CAR激活剂通过该网络调节基因表达的机制。

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