Department of Basic Medical Sciences, University of Arizona College of Medicine, 425 North 5th Street, Phoenix, Arizona 85004-2157, USA School of Mathematical and Natural Sciences, Arizona State University, Phoenix, Arizona 85306, USA.
J Endocrinol. 2014 Jan 8;220(2):165-78. doi: 10.1530/JOE-13-0212. Print 2014 Feb.
The vitamin D receptor (VDR), but not its hormonal ligand, 1,25-dihydroxyvitamin D3 (1,25D), is required for the progression of the mammalian hair cycle. We studied three genes relevant to hair cycle signaling, DKKL1 (Soggy), SOSTDC1 (Wise), and HR (Hairless), to determine whether their expression is regulated by VDR and/or its 1,25D ligand. DKKL1 mRNA was repressed 49-72% by 1,25D in primary human and CCD-1106 KERTr keratinocytes; a functional vitamin D responsive element (VDRE) was identified at -9590 bp in murine Soggy. Similarly, SOSTDC1 mRNA was repressed 41-59% by 1,25D in KERTr and primary human keratinocytes; a functional VDRE was located at -6215 bp in human Wise. In contrast, HR mRNA was upregulated 1.56- to 2.77-fold by 1,25D in primary human and KERTr keratinocytes; a VDRE (TGGTGAgtgAGGACA) consisting of an imperfect direct repeat separated by three nucleotides (DR3) was identified at -7269 bp in the human Hairless gene that mediated dramatic induction, even in the absence of 1,25D ligand. In parallel, a DR4 thyroid hormone responsive element, TGGTGAggccAGGACA, was identified at +1304 bp in the human HR gene that conferred tri-iodothyronine (T3)-independent transcriptional activation. Because the thyroid hormone receptor controls HR expression in the CNS, whereas VDR functions in concert with the HR corepressor specifically in skin, a model is proposed wherein unliganded VDR upregulates the expression of HR, the gene product of which acts as a downstream comodulator to feedback-repress DKKL1 and SOSTDC1, resulting in integration of bone morphogenic protein and Wnt signaling to drive the mammalian hair cycle and/or influencing epidermal function.
维生素 D 受体 (VDR),而不是其激素配体 1,25-二羟维生素 D3(1,25D),是哺乳动物毛发生长周期进展所必需的。我们研究了三个与毛发生长信号相关的基因,DKKL1(Soggy)、SOSTDC1(Wise)和 HR(Hairless),以确定它们的表达是否受 VDR 和/或其 1,25D 配体的调节。1,25D 在原代人角质形成细胞和 CCD-1106 KERTr 中抑制 DKKL1 mRNA 的表达 49-72%;在鼠 Soggy 中鉴定到一个功能性维生素 D 反应元件 (VDRE),位于 -9590bp。同样,1,25D 在 KERTr 和原代人角质形成细胞中抑制 SOSTDC1 mRNA 的表达 41-59%;在人 Wise 中,一个功能性 VDRE 位于 -6215bp。相比之下,1,25D 在原代人角质形成细胞和 KERTr 中使 HR mRNA 的表达上调 1.56-2.77 倍;在人 Hairless 基因中鉴定到一个 VDRE (TGGTGAgtgAGGACA),由三个核苷酸 (DR3) 隔开的不完全直接重复组成,该基因位于 -7269bp 处,介导了显著的诱导作用,即使在没有 1,25D 配体的情况下也是如此。与此同时,在人 HR 基因的+1304bp 处鉴定到一个 DR4 甲状腺激素反应元件 TGGTGAggccAGGACA,该元件赋予三碘甲状腺原氨酸 (T3) 非依赖性转录激活。由于甲状腺激素受体在中枢神经系统中控制 HR 的表达,而 VDR 与 HR 核心抑制因子协同作用,仅在皮肤中发挥作用,因此提出了一个模型,其中无配体的 VDR 上调 HR 的表达,其产物作为下游共调节剂反馈抑制 DKKL1 和 SOSTDC1,从而整合骨形态发生蛋白和 Wnt 信号以驱动哺乳动物毛发生长和/或影响表皮功能。