Phytol metabolites are circulating dietary factors that activate the nuclear receptor RXR

被引:149
作者
Kitareewan, S
Burka, LT
Tomer, KB
Parker, CE
Deterding, LJ
Stevens, RD
Forman, BM
Mais, DE
Heyman, RA
McMorris, T
Weinberger, C
机构
[1] NIEHS,ORPHAN RECEPTOR GRP,RES TRIANGLE PK,NC 27709
[2] NIEHS,CHEM METAB & TOXICOKINET GRP,RES TRIANGLE PK,NC 27709
[3] NIEHS,MASS SPECTROMETRY GRP,RES TRIANGLE PK,NC 27709
[4] DUKE UNIV,MED CTR,DEPT PEDIAT,DIV MED GENET,MASS SPECTROMETRY FACIL,DURHAM,NC 27710
[5] SALK INST BIOL STUDIES,GENE EXPRESS LAB,LA JOLLA,CA 92037
[6] LIGAND PHARMACEUT INC,SAN DIEGO,CA 92121
[7] UNIV CALIF SAN DIEGO,DEPT CHEM,LA JOLLA,CA 92037
关键词
D O I
10.1091/mbc.7.8.1153
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RXR is a nuclear receptor that plays a central role in cell signaling by pairing with a host of other receptors. Previously, 9-cis-retinoic acid (9cRA) was defined as a potent RXR activator. Here we describe a unique RXR effector identified from organic extracts of bovine serum by following RXR-dependent transcriptional activity. Structural analyses of material in active fractions pointed to the saturated diterpenoid phytanic acid, which induced RXR-dependent transcription at concentrations between 4 and 64 mu M. Although 200 times more potent than phytanic acid, 9cRA was undetectable in equivalent amounts of extract and cannot be present at a concentration that could account for the activity. Phytenic acid, another phytol metabolite, was synthesized and stimulated RXR with a potency and efficacy similar to phytanic acid. These metabolites specifically displaced [H-3]-9cRA from RXR with K-i values of 4 mu M, indicating that their transcriptional effects are mediated by direct receptor interactions. Phytol metabolites are compelling candidates for physiological effecters, because their RXR binding affinities and activation potencies match their micromolar circulating concentrations. Given their exclusive dietary origin, these chlorophyll metabolites may represent essential nutrients that coordinate cellular metabolism through RXR-dependent signaling pathways.
引用
收藏
页码:1153 / 1166
页数:14
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