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P8.113
Cultured
Sebocytes: a model for studies on the regulation of steroid acute regulatory
protein and cutaneous steroidogenesis
W. Chen1, C.-C. Yang2, H.-M. Sheu2,
Ch.C. Zouboulis3
1Department of Dermatology, Chang Gung
University, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; 2Department of Dermatology, College of Medicine,
National Cheng Kung University, Tainan, Taiwan; Department of Dermatology, Charité University
Medicine Berlin, Campus Benjamin Franklin, Berlin, Germany
Objectives: The sebaceous gland is a steroidogenic
organ similar to gonads and adrenal cortex, possessing all the enzymes required
for steroid sex hormone synthesis and metabolism. Steroidogenic acute regulatory protein (StAR)
regulates the first committed and rate-limited step of steroid biosynthesis by
controlling the delivery of cholesterol from the outer to the inner membrane of
mitochondria, where the P450scc complex is located. Steroidogenic factor-1
(SF-1) is a positive regulator stimulating the gene expression of StAR. Dosage
sensitive sex reversal adrenal hypoplasia congenita critical region on the
X-chromosome gene-1 (DAX-1) negatively regulates StAR gene expression. On the
other hand, SRY-related HMG-box-transcription factor (SOX-9) can
consistently upregulate SF-1 expression.
Methods: Using
immunostaining, RT-PCR and in situ hybridisation, we tried to identify
and localize the expression of StAR, SF-1, DAX-1 and SOX-9 in sebaceous glands
and immortalized human SZ95 sebocytes.
Results: Immunocytochemistry displayed strong
nuclear expression of DAX1 in basal cells of sebaceous glands. In situ hybridization
study showed SOX9 mRNA mainly localized in the cytoplasm of the basal cell
layer. SZ95 sebocytes expressed mRNA for StAR, SOX9 and DAX1. Treatment of the cultured SZ95 cells with
10–6 M genistein,
one of the major soya isoflavones, enhanced DAX1 protein expression at 6 h and 48 h.
Conclusion:
Like sebaceous glands, SZ95 sebocytes express StAR and StAR regulatory
proteins. Cultured SZ95 sebocytes may serve as a model to investigate StAR
regulation and control of steroidogenesis.
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