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Cutting Edge: AhR Is a Molecular Target of Calcitriol in Human T Cells
Author(s) -
Mariko Takami,
Kotaro Fujimaki,
Michael I. Nishimura,
Makio Iwashima
Publication year - 2015
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.1500344
Subject(s) - calcitriol , calcitriol receptor , transcription factor , vitamin d and neurology , effector , t cell , t cell receptor , ectopic expression , biology , aryl hydrocarbon receptor , immunology , microbiology and biotechnology , chemistry , cancer research , endocrinology , immune system , biochemistry , gene
The immunoregulatory functions of vitamin D have been well documented in various immunological disorders, including multiple sclerosis, arthritis, and asthma. IL-10 is considered a chief effector molecule that promotes the vitamin D-induced immunosuppressive states of T cells and accessory cells. In this article, we demonstrate that the active form of vitamin D, 1,25-dihydroxyvitamin D3 (calcitriol), has a profound inhibitory effect on the development of human Th9, a CD4 T cell subset that is highly associated with asthma, in an IL-10-independent manner. Our data show that calcitriol represses the expression of BATF, a transcription factor essential for Th9, via suppressing the expression of aryl hydrocarbon receptor, without an increase in IL-10. The data show a novel link between vitamin D and two key transcription factors involved in T cell differentiation.

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