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Characterization of the vitamin D endocrine system in human sebocytes in vitro
Authors:Christina Krämer  Holger Seltmann  Markus Seifert  Wolfgang Tilgen  Christos C Zouboulis  Jörg Reichrath
Institution:1. Division of Dermatology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA;2. Department of Dermatology, College of Medicine, Dankook University, Seoul, South Korea;3. Department of Medicine Statistics Core, David Geffen School of Medicine at UCLA, Los Angeles, California, USA;4. Department of Dermatology, Greater Los Angeles Healthcare System Veterans Affairs, Los Angeles, California, USA;1. Institute of Molecular Animal Breeding and Biotechnology, Gene Center, LMU Munich, Munich, Germany;2. Laboratory of Cutaneous Physiopathology and Integrated Center of Metabolomics Research, San Gallicano Dermatologic Institute, IRCCS, Rome, Italy;3. Departments of Dermatology, Venereology, Allergology and Immunology, Dessau Medical Center, Dessau, Germany;4. Department of Medicine, Baylor College of Medicine, Houston, TX, USA;5. Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA
Abstract:Sebocytes are sebum-producing cells that form the sebaceous glands. We investigated the role of sebocytes as target cells for vitamin D metabolites and the existence of an enzymatic machinery for the local synthesis and metabolism of 1,25-dihydroxyvitamin D3 1,25(OH)2D3, calcitriol], the biologically active vitamin D metabolite, in these cell types. Expression of vitamin D receptor (VDR), vitamin D-25-hydroxylase (25OHase), 25-hydroxyvitamin D-1α-hydroxylase (1αOHase), and 1,25-dihydroxyvitamin D-24-hydroxylase (24OHase) was detected in SZ95 sebocytes in vitro using real time quantitative polymerase chain reaction. Splice variants of 1αOHase were identified by nested touchdown polymerase chain reaction. We demonstrated that incubation of SZ95 sebocytes with 1,25(OH)2D3 resulted in a cell culture condition-, time-, and dose-dependent modulation of cell proliferation, cell cycle regulation, lipid content and interleukin-6/interleukin-8 secretion in vitro. RNA expression of VDR and 24OHase was upregulated along with vitamin D analogue treatment. Although several other splice variants of 1αOHase were detected, our findings indicate that the full length product represents the major 1αOHase gene product in SZ95 cells. In conclusion, SZ95 sebocytes express VDR and the enzymatic machinery to synthesize and metabolize biologically active vitamin D analogues. Sebocytes represent target cells for biologically active metabolites. Our findings indicate that the vitamin D endocrine system is of high importance for sebocyte function and physiology. We conclude that sebaceous glands represent potential targets for therapy with vitamin D analogues or for pharmacological modulation of 1,25(OH)2D3 synthesis/metabolism.
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