Abstract

1α,25-Dihydroxyvitamin D 3 (1,25-(OH) 2-D 3), the active metabolite of vitamin D, can inhibit NF-κB activity in human MRC-5 fibroblasts, targeting DNA binding of NF-κB but not translocation of its subunits p50 and p65. The partial inhibition of NF-κB DNA binding by 1,25-(OH) 2-D 3 is dependent on de novo protein synthesis, suggesting that 1,25-(OH) 2-D 3 may regulate expression of cellular factors which contribute to reduced DNA binding of NF-κB. Although NF-κB binding is decreased by 1,25-(OH) 2-D 3 in MRC-5 cells, IL-8 and IL-6 mRNA levels are only moderately downregulated, demonstrating that inhibition of NF-κB DNA binding alone is not sufficient for optimal downregulation of these genes.

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