Vitamin D receptor (VDR)-mediated actions of 1alpha,25(OH)2vitamin D3: genomic and non-genomic mechanisms.

摘要

The conformationally flexible secosteroid, 1alpha,25(OH)(2)vitamin D(3) (1alpha,25(OH)(2)D(3)) initiates biological responses via binding to the vitamin D receptor (VDR). The VDR contains two overlapping ligand binding sites, a genomic pocket (VDR-GP) and an alternative pocket (VDR-AP), that respectively bind a bowl-like ligand configuration (gene transcription) or a planar-like ligand shape (rapid responses). When occupied by 1alpha,25(OH)(2)D(3), the VDR-GP interacts with the retinoid X receptor to form a heterodimer that binds to vitamin D responsive elements in the region of genes directly controlled by 1alpha,25(OH)(2)D(3). By recruiting complexes of either coactivators or corepressors, activated VDR modulates the transcription of genes encoding proteins that promulgate the traditional genomic functions of vitamin D, including signaling intestinal calcium and phosphate absorption to effect skeletal and calcium homeostasis. 1alpha,25(OH)(2)D(3)/VDR control of gene expression and rapid responses also delays chronic diseases of aging such as osteoporosis, cancer, type-1 and -2 diabetes, arteriosclerosis, vascular disease, and infection.