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正常人表皮中朗格汉斯细胞和角质形成细胞的HLA I类抗原(重链和轻链)表达:采用免疫金标记法的超微结构定量分析

HLA class I antigen (heavy and light chain) expression by Langerhans cells and keratinocytes of the normal human epidermis: ultrastructural quantitation using immunogold labelling procedure.

作者信息

Gielen V, Schmitt D, Thivolet J

机构信息

INSERM U209, Hôpital E. Herriot, Lyon, France.

出版信息

Arch Dermatol Res. 1988;280(3):131-6. doi: 10.1007/BF00456841.

Abstract

Using an immunogold labelling procedure, we quantified the density of major histocompatibility (MHC) class I antigens on the surface of Langerhans cells (LCs) and keratinocytes of the normal human epidermis. According to ultrastructural features, keratinocytes were divided into three subpopulations: stratum basalis (SBK), stratum spinosum (SSK), and stratum granulosum keratinocytes (SGK), and analyzed separately. For this purpose, three monoclonal antibodies (MCAs) were employed: an anti-HLA A,B,C, and anti-B2-microglobulin (B2-m), and a polymorphic anti-HLA A2 Aw69 MCA. Under electron microscopy, quantitative analysis demonstrated: (a) the presence of a high amount of HLA monomorphic determinants on SBK and SSK and moderate but significant labelling of SGK; (b) the very weak density of MHC class I antigens on the surface of epidermal LCs; (c) the expression, at an identical level, of the HLA heavy chain common determinant (HLA A,B,C), B2-m, and the alloantigen HLA A2 by all epidermal cells (ECs) apart from SGKs and LCs that presented far fewer HLA A2 sites than monomorphic determinants (B2-m and HLA A,B,C); (d) the absence of HLA class I on corneocytes and a moderate labelling of melanocytes. A knowledge of the precise quantitative distribution of HLA class I antigens among various cell subpopulations of the normal human epidermis would be very useful for the study and follow-up of cutaneous malignancies that are known to lose these molecules as well as for the understanding of immune responses, especially allospecific, that involve the skin.

摘要

我们采用免疫金标记法,对正常人表皮中朗格汉斯细胞(LC)和角质形成细胞表面主要组织相容性复合体(MHC)I类抗原的密度进行了定量分析。根据超微结构特征,角质形成细胞被分为三个亚群:基底细胞层角质形成细胞(SBK)、棘细胞层角质形成细胞(SSK)和颗粒层角质形成细胞(SGK),并分别进行分析。为此,我们使用了三种单克隆抗体(MCA):一种抗HLA A、B、C和抗β2微球蛋白(B2-m),以及一种多态性抗HLA A2 Aw69 MCA。在电子显微镜下,定量分析显示:(a)SBK和SSK上存在大量HLA单态决定簇,SGK有中度但显著的标记;(b)表皮LC表面MHC I类抗原密度非常低;(c)除SGK和LC外,所有表皮细胞(EC)均以相同水平表达HLA重链共同决定簇(HLA A、B、C)、B2-m和同种异体抗原HLA A2,SGK和LC上的HLA A2位点比单态决定簇(B2-m和HLA A、B、C)少得多;(d)角质形成细胞上不存在HLA I类抗原,黑素细胞有中度标记。了解正常人表皮各种细胞亚群中HLA I类抗原的确切定量分布,对于研究已知会丢失这些分子的皮肤恶性肿瘤以及理解涉及皮肤的免疫反应,尤其是同种特异性免疫反应,将非常有用。

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