Fundamental Research Laboratories, KOSE Corporation, 1-18-4 Azusawa, Itabashi-ku, Tokyo 174-0051, Japan.
J Dermatol Sci. 2010 Mar;57(3):192-8. doi: 10.1016/j.jdermsci.2009.12.014. Epub 2010 Jan 15.
The stratum corneum (SC) plays an important role in cutaneous barrier function. Recent clarification of the pathophysiology of several keratoses has suggested that adhesive molecules contribute not only to SC construction but also to SC barrier function.
The purpose of this study is to clarify how the distribution of adhesion molecules on corneocytes contributes to the construction of the SC and the overall organization and function of the cutaneous barrier.
To investigate the distribution of desmoglein 1 (Dsg1), which may be a main component of corneodesmosomes (CDSs) in the SC, we used a bidimensional observation method using tape-stripped corneocytes and several immunohistochemical techniques to demonstrate the distribution of Dsg1 and to deduce internal events in the SC.
Immunofluorescence labeling showed that Dsg1 distributed on corneocytes of the outermost SC with a characteristic pattern at the periphery, or over the entire surface, and differences in this distribution pattern correlated with the transepidermal water loss (TEWL). Furthermore, electron microscopic analysis showed that (1) Dsg1 was localized on CDSs involved in adhesion, and (2) CDSs on the periphery of corneocytes contributed to the generation of the characteristic basket-weave structure.
We explored the distribution pattern of Dsg1 in the SC via a non-invasive investigation tool. Our findings indicate the significance of adhesion molecules in the formation and function of the SC, and suggest that adhesion molecules are one of the important elements in barrier formation in addition to corneocytes, which act as bricks, and intercellular lipids, which act as mortar.
角质层(SC)在皮肤屏障功能中起着重要作用。最近对几种角化病的病理生理学的阐明表明,黏附分子不仅有助于 SC 的构建,而且有助于 SC 屏障功能。
本研究旨在阐明细胞间黏附分子在角质细胞上的分布如何有助于 SC 的构建以及皮肤屏障的整体组织和功能。
为了研究桥粒芯糖蛋白 1(Dsg1)的分布,它可能是 SC 中桥粒(CDS)的主要成分,我们使用了二维观察方法,用胶带剥离的角质细胞和几种免疫组织化学技术来证明 Dsg1 的分布,并推断 SC 中的内部事件。
免疫荧光标记显示,Dsg1 分布在 SC 最外层角质细胞的表面,呈特征性的边缘模式,或整个表面,这种分布模式的差异与经皮水分流失(TEWL)有关。此外,电子显微镜分析显示:(1)Dsg1 定位于参与黏附的 CDS 上;(2)角质细胞边缘的 CDS 有助于产生特征性的篮状结构。
我们通过非侵入性的研究工具探索了 Dsg1 在 SC 中的分布模式。我们的发现表明黏附分子在 SC 的形成和功能中的重要性,并表明黏附分子是除了作为砖的角质细胞和作为灰浆的细胞间脂质之外,形成屏障的重要因素之一。