Cutting Edge: Progesterone Directly Upregulates Vitamin D Receptor Gene Expression for Efficient Regulation of T Cells by Calcitriol
Author(s) -
Shankar Thangamani,
Myughoo Kim,
Youngmin Son,
Xinxin Huang,
Hee Joo Kim,
Jee H. Lee,
Jungyoon Cho,
Benjamin J. Ulrich,
Hal E. Broxmeyer,
Chang H. Kim
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1401923
Subject(s) - calcitriol receptor , calcitriol , nuclear receptor , endocrinology , medicine , immune system , receptor , hormone , microbiology and biotechnology , vitamin d and neurology , biology , chemistry , cancer research , gene , transcription factor , immunology , biochemistry
The two nuclear hormone receptor ligands progesterone and vitamin D (vit.D) play important roles in regulating T cells. The mechanism that connects these two hormones in regulating T cells has not been established. In this study, we report that progesterone is a novel inducer of vit.D receptor (VDR) in T cells and makes T cells highly sensitive to calcitriol. At the molecular level, the induction by progesterone is mediated by two progesterone receptor-binding elements in the intron region after the first noncoding exon of the human VDR gene. Increased expression of VDR by progesterone allows highly sensitive regulation of T cells by vit.D even when vit.D levels are suboptimal. This novel regulatory pathway allows enhanced induction of regulatory T cells but suppression of Th1 and Th17 cells by the two nuclear hormones. The results have significant ramifications in effective regulation of T cells to prevent adverse immune responses during pregnancy.
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