Young Christina A, Eckert Richard L, Adhikary Gautam, Crumrine Debra, Elias Peter M, Blumenberg Miroslav, Rorke Ellen A
Departments of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Departments of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland, USA; Department of Dermatology, University of Maryland School of Medicine, Baltimore, Maryland, USA; Department of Reproductive Biology, University of Maryland School of Medicine, Baltimore, Maryland, USA; Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland, USA.
J Invest Dermatol. 2017 Sep;137(9):1868-1877. doi: 10.1016/j.jid.2017.04.032. Epub 2017 May 16.
AP1 transcription factors are important controllers of gene expression in the epidermis, and altered AP1 factor function can perturb keratinocyte proliferation and differentiation. However, our understanding of how AP1 signaling changes may underlie or exacerbate skin disease is limited. We have shown that inhibiting AP1 factor function in suprabasal adult epidermis leads to reduced filaggrin levels and to a phenotype that resembles the genetic disorder ichthyosis vulgaris. We now show that inhibiting AP1 factor function during development in embryonic epidermis produces marked phenotypic changes including reduced filaggrin mRNA and protein levels, compromised barrier function, marked ultrastructural change, and enhanced dehydration susceptibility that resembles the phenotype observed in the flaky tail mouse, a model for ichthyosis vulgaris. In addition, the AP1 factor-deficient newborn mice display a collodion membrane phenotype that is not observed in flaky tail mice or in newborn individuals with ichthyosis vulgaris but is present in other forms of ichthyosis. This mixed phenotype suggests the need for a better understanding of the possible role of filaggrin loss and AP1 transcription factor deficiency in ichthyoses and collodion membrane formation.
AP1转录因子是表皮中基因表达的重要调控因子,AP1因子功能的改变会扰乱角质形成细胞的增殖和分化。然而,我们对AP1信号变化如何成为皮肤病的潜在病因或加重病情的了解有限。我们已经表明,在成人表皮的基底上层抑制AP1因子功能会导致丝聚合蛋白水平降低,并产生一种类似于遗传性疾病寻常型鱼鳞病的表型。我们现在表明,在胚胎表皮发育过程中抑制AP1因子功能会产生明显的表型变化,包括丝聚合蛋白mRNA和蛋白质水平降低、屏障功能受损、明显的超微结构变化以及脱水敏感性增强,这类似于在片状尾巴小鼠(一种寻常型鱼鳞病模型)中观察到的表型。此外,AP1因子缺陷的新生小鼠表现出一种火棉胶膜表型,这种表型在片状尾巴小鼠或患有寻常型鱼鳞病的新生儿个体中未观察到,但在其他形式的鱼鳞病中存在。这种混合表型表明需要更好地了解丝聚合蛋白缺失和AP1转录因子缺陷在鱼鳞病和火棉胶膜形成中的可能作用。