Kariniemi A L, Lehto V P, Virtanen I
Br J Dermatol. 1983 Nov;109(5):531-7. doi: 10.1111/j.1365-2133.1983.tb07675.x.
Surface glycoproteins of cultured human keratinocytes from normal skin and uninvolved psoriatic epidermis, isolated by the suction blister method, were studied by two different methods. Cells were cultured on collagen-coated culture dishes and showed a fibrillar keratin-specific staining by immunofluorescence. Surface labelling experiments using the neuraminidase/galactose oxidase/sodium borohydride method (which labels the penultimate galactose moieties of glycoproteins) revealed one major glycoprotein with Mr 53 kD (kilodaltons) both in normal keratinocytes and in keratinocytes from uninvolved psoriatic skin. The periodate/sodium borohydride method (which labels the terminal sialic acids in glycoproteins) by contrast revealed three major glycoproteins, with Mr 53 kD to 63 kD, in normal keratinocytes but only a single major glycoprotein, with Mr 53 kD, in keratinocytes from uninvolved psoriatic skin. Treatment of cultured keratinocytes with etretinate appeared to restore the normal pattern of surface glycoproteins in uninvolved psoriatic keratinocytes.
采用两种不同方法,对通过水疱抽吸法分离得到的来自正常皮肤及未受累银屑病表皮的培养人角质形成细胞的表面糖蛋白进行了研究。细胞在胶原包被的培养皿上培养,通过免疫荧光显示出丝状角蛋白特异性染色。使用神经氨酸酶/半乳糖氧化酶/硼氢化钠法(标记糖蛋白的倒数第二个半乳糖部分)进行的表面标记实验表明,正常角质形成细胞和未受累银屑病皮肤的角质形成细胞中均有一种主要糖蛋白,其分子量为53千道尔顿(kD)。相比之下,高碘酸盐/硼氢化钠法(标记糖蛋白中的末端唾液酸)显示,正常角质形成细胞中有三种主要糖蛋白,分子量在53 kD至63 kD之间,但未受累银屑病皮肤的角质形成细胞中只有一种主要糖蛋白,分子量为53 kD。用阿维A酯处理培养的角质形成细胞似乎可使未受累银屑病角质形成细胞的表面糖蛋白恢复正常模式。