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PLoS Genet. 2015 Jun 1;11(6):e1005213. doi: 10.1371/journal.pgen.1005213. eCollection 2015 Jun.

9-cis-13,14-Dihydroretinoic Acid Is an Endogenous Retinoid Acting as RXR Ligand in Mice.

Author information

1
Department of Biochemistry and Molecular Biology, Faculty of Medicine, Debrecen, Hungary; Paprika Bioanalytics BT, Debrecen, Hungary.
2
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France; Inserm, U 964; CNRS UMR 7104, Université de Strasbourg, Strasbourg, France.
3
DE-MTA "Lendület" Immunogenomics Research Group, University of Debrecen, Debrecen, Hungary.
4
Departamento de Química Orgánica and CINBIO, Facultad de Química, Universidade de Vigo, Vigo, Spain; Instituto de Investigación Biomédica de Vigo (IBIV), Vigo, Spain.
5
Paprika Bioanalytics BT, Debrecen, Hungary.

Abstract

The retinoid X receptors (RXRs) are ligand-activated transcription factors which heterodimerize with a number of nuclear hormone receptors, thereby controlling a variety of (patho)-physiological processes. Although synthetic RXR ligands are developed for the treatment of various diseases, endogenous ligand(s) for these receptors have not been conclusively identified. We show here that mice lacking cellular retinol binding protein (Rbp1-/-) display memory deficits reflecting compromised RXR signaling. Using HPLC-MS and chemical synthesis we identified in Rbp1-/- mice reduced levels of 9-cis-13,14-dihydroretinoic acid (9CDHRA), which acts as an RXR ligand since it binds and transactivates RXR in various assays. 9CDHRA rescues the Rbp1-/- phenotype similarly to a synthetic RXR ligand and displays similar transcriptional activity in cultured human dendritic cells. High endogenous levels of 9CDHRA in mice indicate physiological relevance of these data and that 9CDHRA acts as an endogenous RXR ligand.

PMID:
26030625
PMCID:
PMC4451509
DOI:
10.1371/journal.pgen.1005213
[Indexed for MEDLINE]
Free PMC Article

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