Marshall D, Hardman M J, Nield K M, Byrne C
School of Biological Sciences, University of Manchester, 3.239 Stopford Building, Oxford Road, Manchester M13 9PT, United Kingdom.
Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13031-6. doi: 10.1073/pnas.231489198.
Barrier activity of skin and internal barrier-forming epithelial linings are conferred by a lipid-corneocyte structure (stratum corneum in skin). The integrity of the corneocytes depends on the outer cornified envelope and is essential for maintenance of barrier function. During epidermal development and differentiation, proteins are sequentially incorporated into the envelope via action of epidermal transglutaminases in a well documented process. However, recent knockouts of major cornified envelope constituents have failed to disrupt barrier function significantly, suggesting that additional unidentified components are involved. We report a new gene cluster in the epidermal differentiation complex at human 1q21 encoding a family of 18 proteins that are substrates for epidermal transglutaminases. These proteins incorporate into the cornified envelope late in development and late in the process of envelope maturation during epidermal differentiation. The genes cluster within the epidermal differentiation complex according to expression pattern, i.e., epidermally expressed proteins cluster together while proteins from internal barrier-forming epithelia also cluster. We propose that these proteins modulate barrier activity over the surface of the animal, in a manner analogous to that proposed for the well characterized cornified envelope precursors, the small proline-rich proteins. To emphasize the incorporation of these proteins late in envelope assembly, we call the human proteins late envelope proteins.
皮肤的屏障活性以及内部形成屏障的上皮内衬是由脂质-角质形成细胞结构(皮肤中的角质层)赋予的。角质形成细胞的完整性取决于外层角化包膜,并且对于维持屏障功能至关重要。在表皮发育和分化过程中,蛋白质通过表皮转谷氨酰胺酶的作用依次整合到包膜中,这是一个有充分文献记载的过程。然而,最近对主要角化包膜成分的基因敲除未能显著破坏屏障功能,这表明还涉及其他未鉴定的成分。我们报告了人类1q21表皮分化复合体中的一个新基因簇,其编码一个由18种蛋白质组成的家族,这些蛋白质是表皮转谷氨酰胺酶的底物。这些蛋白质在发育后期以及表皮分化过程中包膜成熟的后期整合到角化包膜中。这些基因根据表达模式在表皮分化复合体内聚集,即表皮表达的蛋白质聚集在一起,而来自内部形成屏障的上皮的蛋白质也聚集在一起。我们提出,这些蛋白质以类似于已充分表征的角化包膜前体——富含脯氨酸的小蛋白的方式,调节动物体表的屏障活性。为了强调这些蛋白质在包膜组装后期的整合,我们将人类的这些蛋白质称为晚期包膜蛋白。