BMB Reports · 2010 · 32 citations · 17 references
Life SciencesEndocrinologyMolecular BiologyCell SignalingGene ExpressionTranscriptional RegulationAndrogen PhysiologyHormone Gene RegulationSteroid Hormone BiochemistrySteroid Hormone SignalingSteroidogenesis RegulationSteroidogenic EnzymesAndrogen Action In SkinAndrogen MetabolismAndrogen MetabolitesGene Expression Control In SteroidogenesisMammalian Hair CellsSteroidogenesis Pathway RegulationSteroidogenic Enzyme RegulationSteroidogenic Gene Regulation
In a previous study, we recently claimed that dihydrotestosterone (DHT)-inducible dickkopf-1 (DKK-1) expression is one of the key factors involved in androgen-potentiated balding. We also demonstrated that L-ascorbic acid 2-phosphate (Asc 2-P) represses DHT-induced DKK-1 expression in cultured dermal papilla cells (DPCs). Here, we investigated whether or not L-threonate could attenuate DHT-induced DKK-1 expression. We observed via RT-PCR analysis and enzyme-linked immunosorbent assay that DHT-induced DKK-1 expression was attenuated in the presence of L-threonate. We also found that DHT-induced activation of DKK-1 promoter activity was significantly repressed by L-threonate. Moreover, a co-culture system featuring outer root sheath (ORS) keratinocytes and DPCs showed that DHT inhibited the growth of ORS cells, which was then significantly reversed by L-threonate. Collectively, these results indicate that L-threonate inhibited DKK-1 expression in DPCs and therefore is a good treatment for the prevention of androgen-driven balding.
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