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培养的角质形成细胞和成纤维细胞中纤连蛋白、IV型前胶原和230kDa大疱性类天疱疮抗原基因的表达:聚合酶链反应在检测少量信使核糖核酸中的应用

Expression of laminin, type IV procollagen and 230 kDa bullous pemphigoid antigen genes by keratinocytes and fibroblasts in culture: application of the polymerase chain reaction for detection of small amounts of messenger RNA.

作者信息

Nomura K, Sugawara T, Sato T, Sawamura D, Hashimoto I, Sugita Y, Uitto J

机构信息

Department of Dermatology, Hirosaki University School of Medicine, Japan.

出版信息

Arch Dermatol Res. 1994;286(7):408-13. doi: 10.1007/BF00371801.

Abstract

In order to clarify whether keratinocytes and/or fibroblasts express genes encoding basement membrane zone macromolecules, we examined laminin, type IV collagen and 230 kDa bullous pemphigoid antigen (BPAG1) gene expression in keratinocytes and fibroblasts in culture. Northern transfer analysis revealed the presence of specific mRNA transcripts for alpha 1(IV) and alpha 2(IV) chains of type IV collagen as well as B1 and B2 chains of laminin in both fibroblast and keratinocyte RNA. Laminin A mRNA, however, was detected in fibroblasts but not in keratinocytes. In contrast, BPAG1 mRNA was detected in keratinocytes but not in fibroblasts using the same RNA preparations. A polymerase chain reaction (PCR) using laminin A and BPAG1-specific primers produced amplified DNAs with the predicted sizes in reverse-transcripted cDNA derived from keratinocyte and fibroblast RNA, respectively. These results provide evidence that normal human skin keratinocytes and fibroblasts express genes encoding laminin A, B1, B2, alpha 1(IV), and BPAG1 at a steady-state level. Moreover, the PCR for detecting small amounts of mRNA suggested that both keratinocytes and fibroblasts can be utilized for the analysis of DNA mutations in inherited skin diseases affecting the basement membrane zone, such as epidermolysis bullosa.

摘要

为了阐明角质形成细胞和/或成纤维细胞是否表达编码基底膜区大分子的基因,我们检测了培养的角质形成细胞和成纤维细胞中层粘连蛋白、IV型胶原和230kDa大疱性类天疱疮抗原(BPAG1)的基因表达。Northern印迹分析显示,在成纤维细胞和角质形成细胞RNA中均存在IV型胶原α1(IV)和α2(IV)链以及层粘连蛋白B1和B2链的特异性mRNA转录本。然而,层粘连蛋白A mRNA仅在成纤维细胞中检测到,而在角质形成细胞中未检测到。相反,使用相同的RNA制剂,在角质形成细胞中检测到BPAG1 mRNA,而成纤维细胞中未检测到。使用层粘连蛋白A和BPAG1特异性引物进行的聚合酶链反应(PCR)分别在源自角质形成细胞和成纤维细胞RNA的逆转录cDNA中产生了预测大小的扩增DNA。这些结果证明,正常人类皮肤角质形成细胞和成纤维细胞在稳态水平上表达编码层粘连蛋白A、B1、B2、α1(IV)和BPAG1的基因。此外,用于检测少量mRNA的PCR表明,角质形成细胞和成纤维细胞均可用于分析影响基底膜区的遗传性皮肤病(如大疱性表皮松解症)中的DNA突变。

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