Moll I, Heid H, Franke W W, Moll R
Differentiation. 1987;33(3):254-65. doi: 10.1111/j.1432-0436.1987.tb01565.x.
Biochemical analyses have previously shown that palmar and plantar epidermis, unlike the epidermis of other body sites, contain cytokeratin 9 (Mr 64,000), an unusually large acidic (type I) cytokeratin. Guinea-pig antibodies that specifically and selectively react with bovine and human cytokeratin 9 were used for the immunocytochemical identification of cytokeratin 9 in adult and fetal human epidermis from various body sites. In the epidermis of palms and soles, antibodies against cytokeratin 9 stained a high proportion of the keratinocytes in suprabasal locations. These suprabasal cytokeratin-9-positive keratinocytes were often arranged in vertical columns and concentrated around intraepidermal sweat-gland ducts, but they sometimes also formed extended continuous sheets. In contrast, another type-I component, cytokeratin(s) 10/11, was uniformly distributed among suprabasal keratinocytes. By double-labeling immunofluorescence microscopy using a monoclonal antibody against cytokeratin(s) 10/11, we found that cytokeratin 9 usually appears in cells located one or two layers above the cells in which cytokeratin(s) 10/11 is detected, indicating that most keratinocytes expressing cytokeratin 9 also express cytokeratin(s) 10/11. At other body sites, cytokeratin 9 was only detected in sparsely distributed keratinocytes localized in upper epidermal layers; these cells were scattered or formed small clusters, and often exhibited a conspicuous association with the epidermal portion of eccrine sweat-gland ducts. During human fetal development, cytokeratin 9 was first detected at week 15 of gestation in some suprabasal cells of the foot-sole epidermis and, occasionally, in basal cells. At later fetal stages, most of the cytokeratin-9-positive cells appeared in clusters that were mainly concentrated in glandular ridges and interridges. Our results show that two major types of terminally differentiating keratinocytes can be distinguished in human epidermis, i.e. those that do and those that do not express cytokeratin 9. This special program of keratinocyte differentiation identified by the presence of cytokeratin 9 appears to be related to the morphogenesis of palm and sole epidermis, where this protein is expressed early in fetal life. Possible biological functions of this subset of cytokeratin-9-positive keratinocytes are discussed.
生化分析先前已表明,手掌和足底表皮与身体其他部位的表皮不同,含有细胞角蛋白9(分子量64,000),这是一种异常大的酸性(I型)细胞角蛋白。使用能与牛和人细胞角蛋白9特异性且选择性反应的豚鼠抗体,对来自不同身体部位的成人及胎儿人类表皮中的细胞角蛋白9进行免疫细胞化学鉴定。在手掌和足底表皮中,抗细胞角蛋白9的抗体使基底上层位置的大部分角质形成细胞染色。这些基底上层细胞角蛋白9阳性的角质形成细胞常排列成垂直柱状,并集中在表皮内汗腺导管周围,但它们有时也形成延伸的连续片层。相比之下,另一种I型成分,细胞角蛋白10/11,在基底上层角质形成细胞中均匀分布。通过使用抗细胞角蛋白10/11的单克隆抗体进行双标记免疫荧光显微镜检查,我们发现细胞角蛋白9通常出现在检测到细胞角蛋白10/11的细胞上方一层或两层的细胞中,这表明大多数表达细胞角蛋白9的角质形成细胞也表达细胞角蛋白10/11。在身体其他部位,仅在上层表皮层中稀疏分布的角质形成细胞中检测到细胞角蛋白9;这些细胞分散或形成小簇,并且常与外泌汗腺导管的表皮部分有明显关联。在人类胎儿发育过程中,细胞角蛋白9在妊娠第15周时首次在足底表皮的一些基底上层细胞中检测到,偶尔也在基底细胞中检测到。在胎儿后期阶段,大多数细胞角蛋白9阳性细胞以簇状出现,主要集中在腺嵴和嵴间。我们的结果表明,在人类表皮中可区分出两种主要类型的终末分化角质形成细胞,即表达和不表达细胞角蛋白9的细胞。由细胞角蛋白9的存在所确定的这种特殊的角质形成细胞分化程序似乎与手掌和足底表皮的形态发生有关,在胎儿生命早期该蛋白就在此处表达。本文讨论了细胞角蛋白9阳性角质形成细胞这一亚群可能的生物学功能。