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持久性豆状角化过度症(弗莱格病)的角化不良过程。富含胱氨酸蛋白的异常形成。

Dyskeratotic process of hyperkeratosis lenticularis perstans (Flegel). The abnormal formation of cystine-rich protein.

作者信息

Tezuka T

出版信息

Dermatologica. 1982 Jun;164(6):379-85. doi: 10.1159/000250122.

Abstract

The dyskeratotic changes in the lesions of hyperkeratosis lenticularis perstans were examined electron microscopically and histochemically. Under electron microscopy, the formation of keratohyalin granules was reduced and there was a lack of lamellar granule formation. In addition, the catabolic processes were disturbed, and ribosomal and mitochondrial structures remained, and lipid crystal-like structures were seen in the stratum corneum. The structure of the desmosomes of the stratum corneum was identical to that seen in the stratum spinosum. Staining with thiol-specific, fluorescent reagent, N-(7-dimethylamino-4-methyl-coumarinyl) maleimide (DACM) demonstrated strong fluorescence in the cytoplasm of the stratum corneum and granulosum without reduction by 2-mercaptoethanol. With reduction, moderate fluorescence was only seen at the periphery of the stratum corneum cells. These results indicate that there is a cystine-rich protein in the stratum corneum cells.

摘要

对持久性豆状角化过度症病变中的角化不良变化进行了电子显微镜和组织化学检查。在电子显微镜下,透明角质颗粒的形成减少,且缺乏板层颗粒的形成。此外,分解代谢过程受到干扰,核糖体和线粒体结构保留,角质层中可见脂类晶体样结构。角质层桥粒的结构与棘层中所见相同。用硫醇特异性荧光试剂N-(7-二甲基氨基-4-甲基香豆素基)马来酰亚胺(DACM)染色显示,角质层和颗粒层细胞质中有强荧光,且不被2-巯基乙醇还原。还原后,仅在角质层细胞周边可见中度荧光。这些结果表明角质层细胞中存在富含胱氨酸的蛋白质。

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