Vitamin D Research Today is a free monthly online journal that collates and summarizes the latest research about Vitamin D, including details on sources, melanin, benefits, deficiency, supplements, calcium absorption.

2-Methylene-19-nor-1alpha-hydroxyvitamin D3 analogs inhibit adipocyte differentiation and PPARgamma2 gene transcription.

Thomson B, Ahrens JM, Ntambi JM, DeLuca HF, Clagett-Dame M

Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.

The hormonally active form of vitamin D3, 1alpha,25-dihydroxyvitamin D3 (1,25(OH)2D3), prevents adipogenesis in the 3T3-L1 preadipocyte cell line. In this paper, both a shortened side-chain non-calcemic analog, (20S)-1alpha-hydroxy-2-methylene-19-nor-bishomopregnacalciferol (2MbisP), as well as a highly bone-selective compound, 2-methylene-19-nor-(20S)-1alpha-hydroxyvitamin D3 (2MD), are shown to completely prevent adipocyte differentiation in this cell line. 2MbisP is slightly less potent than 1,25(OH)2D3, whereas 2MD is approximately two orders of magnitude more potent that the parent hormone in preventing adipocyte differentiation. The ability to block differentiation requires binding to the vitamin D receptor. Both 1,25(OH)2D3 and the analogs prevent the induction of the C/EBPalpha and PPARgamma2 transcription factors, which is necessary for terminal differentiation. In contrast, the normal increase in C/EBPbeta protein that occurs shortly after the induction of differentiation occurs both in the presence and absence of vitamin D compounds, and the C/EBPbeta protein appears functional with respect to DNA binding and nuclear localization. Transient transfection studies show that 1,25(OH)2D3 prevents transactivation through the 5' region of the PPARgamma2 promoter, and thus acts at the transcriptional level to inhibit the normal upregulation of PPARgamma2 that occurs during the course of 3T3-L1 cell differentiation.

Published 23 April 2007 in Arch Biochem Biophys, 460(2): 192-201.
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