1α,24(S)-dihydroxyvitamin D2: a biologically active product of 1α-hydroxyvitamin D2 made in the human hepatoma, Hep3B

Author:

Strugnell S1,Byford V1,Makin H L J2,Moriarty R M3,Gilardi R4,LeVan L W5,Knutson J C5,Bishop C W5,Jones G1

Affiliation:

1. Departments of Biochemistry and Medicine, Queen's University, Kingston, Ontario, Canada K7L 3N6 Canada

2. Department of Chemical Pathology, The London Hospital Medical College, University of London, London El 2AD, U.K.

3. Steroids Ltd., Chicago, IL 60612, U.S.A.

4. Laboratory for the Structure of Matter, Naval Research Laboratory, Washington, DC 20375, U.S.A.,

5. Lunar Corporation, Madison, WI 53713, U.S.A.

Abstract

A major metabolite of the vitamin D analogue 1 alpha-hydroxyvitamin D2 in human liver cells in culture has been identified as 1 alpha,24(S)-dihydroxyvitamin D2 [1 alpha,24(S)-(OH)2D2]. 1 alpha-Hydroxyvitamin D3 incubated with the same cells gives rise to predominantly 25- and 27-hydroxylated products. Our identification of 1 alpha,24(S)-dihydroxyvitamin D2 is based on comparisons of the liver cell metabolite with chemically synthesized 1 alpha,24(S)-(OH)2D2 and 1 alpha,24(R)-(OH)2D2 by using HPLC, GC and GC-MS techniques. The stereochemical orientation of the 24-hydroxyl group was inferred after X-ray-crystallographic analysis of the 24(R)-OH epimer. 1 alpha,24(S)-Dihydroxyvitamin D2 binds strongly to the vitamin D receptor and is biologically active in growth hormone and chloramphenicol acetyltransferase reporter gene expression systems in vitro, but binds poorly to rat vitamin D-binding globulin, DBP. We suggest that this metabolite, 1 alpha,24(S)-(OH)2D2, possesses the spectrum of biological properties to be useful as a drug in the treatment of psoriasis, metabolic bone disease and cancer.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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