Li Hongyu, Zhou Longjian, Dai Jun
School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, P. R. China.
Cutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts.
J Cell Physiol. 2018 Jan;233(1):641-650. doi: 10.1002/jcp.25924. Epub 2017 May 19.
Low O pressures present in the microenvironment of epidermis control keratinocyte differentiation and epidermal barrier function through hypoxia inducible factors (HIFs) dependent gene expression. This study focuses on investigating relations of the retinoic acid receptor-related orphan receptor alpha (RORα) to HIF-1α in keratinocytes under hypoxic conditions. The expression level of RORα is significantly elevated under hypoxia in both human and murine keratinocytes. Gene silencing of RORA attenuates hypoxia-stimulated expression of genes related to late differentiation and epidermal barrier function, and leads to an enhanced apoptotic response. While the hypoxic induction of RORα is dependent on HIF-1α, RORα is in turn critical for nuclear accumulation of HIF-1α and activation of HIF transcriptional activity. These results collectively suggest that RORα functions as an important mediator of HIF-1α activities in regulating keratinocyte differentiation/survival and epidermal barrier function during the oxygen sensing stage.
表皮微环境中存在的低氧压力通过缺氧诱导因子(HIFs)依赖的基因表达来控制角质形成细胞的分化和表皮屏障功能。本研究聚焦于探究在缺氧条件下角质形成细胞中视黄酸受体相关孤儿受体α(RORα)与HIF-1α之间的关系。在人和小鼠角质形成细胞中,缺氧条件下RORα的表达水平显著升高。RORA基因沉默减弱了缺氧刺激的与晚期分化和表皮屏障功能相关基因的表达,并导致凋亡反应增强。虽然RORα的缺氧诱导依赖于HIF-1α,但RORα反过来对于HIF-1α的核积累和HIF转录活性的激活至关重要。这些结果共同表明,RORα在氧感应阶段作为HIF-1α活性的重要介质,调节角质形成细胞的分化/存活和表皮屏障功能。