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c-kit配体在人角质形成细胞中的表达。

Expression of c-kit ligand in human keratinocytes.

作者信息

Morita E, Lee D G, Sugiyama M, Yamamoto S

机构信息

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

出版信息

Arch Dermatol Res. 1994;286(5):273-7. doi: 10.1007/BF00387600.

Abstract

The c-kit ligand is expressed on tissue-anchored stromal cells. It plays an important role in the development of c-kit-bearing cells, such as haematopoietic cells, germ cells, mast cells and melanocytes. In the present study, we used the reverse transcriptase-mediated polymerase chain reaction (PCR) technique to investigate whether human keratinocytes are able to express c-kit ligand mRNA. Two sets of primers were designed to distinguish two types of c-kit ligand mRNA (full-length type and spliced type). One set was used to amplify an 882-bp DNA fragment from the full-length type, and a 798-bp DNA fragment from the spliced type. Another set was used to amplify a 375-bp DNA fragment from the full-length type only. A cDNA fragment corresponding to the full-length type mRNA was amplified from a cDNA preparation of cultured human keratinocytes as well as from epidermis obtained by the suction blister technique. This result indicates the spontaneous transcription of full-length type mRNA of the c-kit ligand in human keratinocytes.

摘要

c-kit配体在组织锚定的基质细胞上表达。它在携带c-kit的细胞(如造血细胞、生殖细胞、肥大细胞和黑素细胞)的发育中起重要作用。在本研究中,我们使用逆转录酶介导的聚合酶链反应(PCR)技术来研究人角质形成细胞是否能够表达c-kit配体mRNA。设计了两组引物来区分两种类型的c-kit配体mRNA(全长型和剪接型)。一组用于从全长型扩增882 bp的DNA片段,从剪接型扩增798 bp的DNA片段。另一组仅用于从全长型扩增375 bp的DNA片段。从培养的人角质形成细胞的cDNA制剂以及通过吸疱技术获得的表皮中扩增出与全长型mRNA相对应的cDNA片段。这一结果表明人角质形成细胞中c-kit配体全长型mRNA的自发转录。

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