Akiyama Masashi
Department of Dermatology; Nagoya University Graduate School of Medicine; Nagoya, Japan.
Dermatoendocrinol. 2011 Apr;3(2):107-12. doi: 10.4161/derm.3.2.15136. Epub 2011 Apr 1.
ABCA12 is a member of the large superfamily of ATP-binding cassette (ABC) transporters, which bind and hydrolyze ATP to transport various molecules across limiting membranes or into vesicles. The ABCA subfamily members are thought to be lipid transporters. ABCA12 is a keratinocyte transmembrane lipid transporter protein associated with the transport of lipids in lamellar granules to the apical surface of granular layer keratinocytes. Extracellular lipids, including ceramide, are thought to be essential for skin barrier function. ABCA12 mutations are known to underlie the three main types of autosomal recessive congenital ichthyoses: harlequin ichthyosis, lamellar ichthyosis and congenital ichthyosiform erythroderma. ABCA12 mutations lead to defective lipid transport via lamellar granules in the keratinocytes, resulting in malformation of the epidermal lipid barrier and ichthyosis phenotypes. Studies of ABCA12-deficient model mice indicate that lipid transport by ABCA12 is also indispensable for intact differentiation of keratinocytes.
ABCA12是ATP结合盒(ABC)转运蛋白大家族的成员,该家族通过结合并水解ATP来跨限制膜或向囊泡内转运各种分子。ABCA亚家族成员被认为是脂质转运蛋白。ABCA12是一种角质形成细胞跨膜脂质转运蛋白,与脂质从板层颗粒转运至颗粒层角质形成细胞的顶端表面有关。包括神经酰胺在内的细胞外脂质被认为对皮肤屏障功能至关重要。已知ABCA12突变是常染色体隐性先天性鱼鳞病三种主要类型的病因:丑角样鱼鳞病、板层状鱼鳞病和先天性鱼鳞病样红皮病。ABCA12突变导致角质形成细胞中板层颗粒的脂质转运缺陷,从而导致表皮脂质屏障畸形和鱼鳞病表型。对ABCA12缺陷型模型小鼠的研究表明,ABCA12介导的脂质转运对角质形成细胞的完整分化也必不可少。