Weiss R A, Eichner R, Sun T T
J Cell Biol. 1984 Apr;98(4):1397-406. doi: 10.1083/jcb.98.4.1397.
The polypeptide composition of epidermal keratin varies in disease. To better understand the biological meaning of these variations, we have analyzed keratins from a number of human epidermal diseases by the immunoblot technique using AE1 and AE3 monoclonal antikeratin antibodies. The results reveal a continuous spectrum of keratin expression ranging from one closely resembling the normal in vivo pattern to one almost identical to cultured epidermal keratinocytes. Specifically, a 50-kilodalton (kd) (AE1-positive) and a 58-kd (AE3-positive) keratin are present in all diseases, supporting the concept that they represent "permanent" markers for keratinocytes. A 56.5-kd (AE1) and a 65-67-kd (AE3) keratin, previously shown to be markers for keratinization, are expressed only by lesions retaining a keratinized morphology. A 48-kd (AE1) and a 56-kd (AE3) keratin are present in all hyperproliferative (para- or nonkeratinized) disorders, but not in normal abdominal epidermis or in ichthyosis vulgaris which is a nonhyperproliferative disease. These two keratins have previously been found in various nonepidermal keratinocytes undergoing hyperproliferation, suggesting that these keratins are not epidermis-specific and may represent markers for hyperproliferative keratinocytes in general. In various epidermal diseases, there is a reciprocal expression of the (keratin) markers for hyperproliferation and keratinization, supporting the mutual exclusiveness of the two cellular events. Moreover, our results indicate that, as far as keratin expression is concerned, cultured human epidermal cells resemble and thus may be regarded as a model for epidermal hyperplasia. Finally, the apparent lack of any major, disease-specific keratin changes in the epidermal disorders studied so far implies that keratin abnormalities probably represent the consequence, rather than the cause, of these diseases.
表皮角蛋白的多肽组成在疾病中会发生变化。为了更好地理解这些变化的生物学意义,我们使用AE1和AE3单克隆抗角蛋白抗体,通过免疫印迹技术分析了多种人类表皮疾病中的角蛋白。结果揭示了角蛋白表达的连续谱,范围从与正常体内模式非常相似的一种到几乎与培养的表皮角质形成细胞相同的一种。具体而言,所有疾病中均存在一种50千道尔顿(kd)(AE1阳性)和一种58-kd(AE3阳性)角蛋白,支持了它们代表角质形成细胞“永久性”标志物的概念。先前已证明一种56.5-kd(AE1)和一种65 - 67-kd(AE3)角蛋白是角质化的标志物,仅在保留角质化形态的病变中表达。一种48-kd(AE1)和一种56-kd(AE3)角蛋白存在于所有增殖过度(不全角化或非角化)性疾病中,但在正常腹部表皮或寻常型鱼鳞病(一种非增殖过度性疾病)中不存在。这两种角蛋白先前已在各种增殖过度的非表皮角质形成细胞中发现,表明这些角蛋白并非表皮特异性的,可能总体上代表增殖过度的角质形成细胞的标志物。在各种表皮疾病中,增殖过度和角质化的(角蛋白)标志物存在相互表达,支持了这两种细胞事件的相互排斥性。此外,我们的结果表明,就角蛋白表达而言,培养的人表皮细胞与之相似,因此可被视为表皮增生的模型。最后,在目前所研究的表皮疾病中,明显缺乏任何主要的、疾病特异性的角蛋白变化,这意味着角蛋白异常可能是这些疾病的结果而非原因。