RXR: From Partnership to Leadership in Metabolic Regulations

视黄醇X受体 核受体 维甲酸 细胞生物学 受体 转录因子 生物 信号转导 肝X受体 维甲酸受体 生物化学 化学 基因
作者
Béatrice Desvergne
出处
期刊:Vitamins and hormones [Elsevier BV]
卷期号:75: 1-32 被引量:105
标识
DOI:10.1016/s0083-6729(06)75001-4
摘要

Vitamin A signaling occurs through nuclear receptors recognizing diverse forms of retinoic acid (RA). The retinoic acid receptors (RARs) bind all‐trans RA and its 9‐cis isomer (9‐cis RA). They convey most of the activity of RA, particularly during embryogenesis. The second subset of receptors, the rexinoid receptors (RXRs), binds 9‐cis RA only. However, RXRs are obligatory DNA‐binding partners for a number of nuclear receptors, broadening the spectrum of their biological activity to the corresponding nuclear receptor‐signaling pathways. The present chapter more particularly focuses on RXR‐containing transcriptional complexes for which RXR is not only a structural component necessary for DNA binding but also acts as a ligand‐activated partner. After positioning RXR among the nuclear receptor superfamily in the first part, we will give an overview of three major signaling pathways involved in metabolism, which are sensitive to RXR activation: LXR:RXR, FXR:RXR, and PPAR:RXR. The third and last part is focused on RXR signaling and its potential role in metabolic regulation. Indeed, while the nature of the endogenous ligand for RXR is still in question, as we will discuss herein, a better understanding of RXR activities is necessary to envisage the potential therapeutic applications of synthetic RXR ligands.

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