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人类IgG1类别转换程序的证据。

Evidence for a human IgG1 class switch program.

作者信息

Irsch J, Hendriks R, Tesch H, Schuurman R, Radbruch A

机构信息

Institute for Genetics, University of Cologne, FRG.

出版信息

Eur J Immunol. 1993 Feb;23(2):481-6. doi: 10.1002/eji.1830230227.

Abstract

In activated murine B lymphocytes, immunoglobulin class switch recombination occurs as a highly regulated process which is targeted to distinct switch regions. Here we present first evidence that in human B lymphocytes, switch recombination is targeted to distinct switch regions as well. In a panel of clonally unrelated IgG1-expressing human B cells, immortalized by Epstein-Barr virus (EBV) transformation, seven out of nine cells show switch recombination between S mu and S gamma 1 on both alleles, the active and inactive one. The remaining cells show no switch recombination on the inactive IgH locus. The very strong correlation of switch recombination on both alleles of IgG1-expressing cells proves that class switch recombination to IgG1 is not random but directed in human B lymphocytes.

摘要

在活化的小鼠B淋巴细胞中,免疫球蛋白类别转换重组是一个高度受调控的过程,该过程靶向于不同的转换区域。在此,我们首次提供证据表明,在人类B淋巴细胞中,转换重组同样靶向于不同的转换区域。在一组通过爱泼斯坦-巴尔病毒(EBV)转化永生化的、克隆无关的表达IgG1的人类B细胞中,9个细胞中有7个在两个等位基因(活性和非活性等位基因)上均显示出Sμ和Sγ1之间的转换重组。其余细胞在非活性IgH基因座上未显示转换重组。表达IgG1细胞的两个等位基因上转换重组的高度相关性证明,在人类B淋巴细胞中,向IgG1的类别转换重组并非随机发生,而是定向的。

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