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首页> 外文期刊>Journal of cell biology >Monoclonal antibody analysis of keratin expression in epidermal diseases: a 48- and 56-kdalton keratin as molecular markers for hyperproliferative keratinocytes.
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Monoclonal antibody analysis of keratin expression in epidermal diseases: a 48- and 56-kdalton keratin as molecular markers for hyperproliferative keratinocytes.

机译:表皮疾病中角蛋白表达的单克隆抗体分析:48kdalton和56kdalton角蛋白作为过度增生角质形成细胞的分子标记。

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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.
机译:表皮角蛋白的多肽组成因疾病而异。为了更好地理解这些变异的生物学意义,我们已经使用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的角蛋白。结果揭示了角蛋白表达的连续光谱,范围从非常类似于正常体内模式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,在所有疾病中均存在50千达尔顿(kd)(AE1阳性)和58 kd(AE3阳性)角蛋白,支持了它们代表角质形成细胞“永久”标记的概念。先前显示为角化标记的56.5 kd(AE1)和65-67 kd(AE3)角蛋白仅由保留角化形态的病变表达。 48 kd(AE1)和56 kd(AE3)角蛋白存在于所有过度增生性(副角化或非角化)疾病中,但不存在于正常的腹部表皮或非鱼鳞病中,后者是一种非过度增生性疾病。先前已经在经历过度增殖的各种非表皮角质形成细胞中发现了这两种角蛋白,这表明这些角蛋白不是表皮特异性的,并且通常可以代表过度增殖性角质形成细胞的标记。在各种表皮疾病中,过度增生和角化作用的(角蛋白)标记相互表达,支持两种细胞事件的相互排斥。而且,我们的结果表明,就角蛋白表达而言,培养的人表皮细胞类似,因此可以被认为是表皮增生的模型。最后,到目前为止研究的表皮疾病中明显缺乏任何主要的,特定于疾病的角蛋白变化,这表明角蛋白异常可能代表了这些疾病的后果,而不是原因。

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