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VpreB1/VpreB2/λ5三缺陷小鼠表现出B细胞发育受损,但IgH基因座存在功能性等位基因排斥。

VpreB1/VpreB2/lambda 5 triple-deficient mice show impaired B cell development but functional allelic exclusion of the IgH locus.

作者信息

Shimizu Takeyuki, Mundt Cornelia, Licence Steve, Melchers Fritz, Mårtensson Inga-Lill

机构信息

Basel Institute for Immunology, Basel, Switzerland.

出版信息

J Immunol. 2002 Jun 15;168(12):6286-93. doi: 10.4049/jimmunol.168.12.6286.

Abstract

At the precursor B cell stage during bone marrow B cell development, Ig muH chain associates with surrogate L (SL) chain, which is encoded by the three genes VpreB1, VpreB2, and lambda 5, to form the pre-B cell receptor (pre-BCR). Surface expression of the pre-BCR is believed to signal both proliferation and allelic exclusion of the IgH locus. Mice which lack either VpreB1/VpreB2 or lambda 5 show a lack of precursor B cell expansion but normal IgH allelic exclusion. This would suggest that one of either lambda 5 or VpreB can make a pre-BCR-like complex which is still able to signal allelic exclusion but not proliferation. To investigate this, we established mice lacking all components of the SL chain. These mice showed severely impaired B cell development which was similar to that previously found in mice lacking either lambda 5 or VpreB1/VpreB2. Surprisingly, the IgH locus was still allelically excluded and thus the SL chain appears not to be involved in allelic exclusion.

摘要

在骨髓B细胞发育的前体B细胞阶段,Ig μ重链与由VpreB1、VpreB2和λ5这三个基因编码的替代轻链(SL链)结合,形成前B细胞受体(pre-BCR)。据信,pre-BCR的表面表达对IgH基因座的增殖和等位基因排斥均发出信号。缺乏VpreB1/VpreB2或λ5的小鼠表现出前体B细胞扩增缺陷,但IgH等位基因排斥正常。这表明λ5或VpreB之一能够形成类似pre-BCR的复合物,该复合物仍能发出等位基因排斥信号,但不能发出增殖信号。为了对此进行研究,我们构建了缺乏SL链所有组分的小鼠。这些小鼠表现出严重受损的B细胞发育,这与先前在缺乏λ5或VpreB1/VpreB2的小鼠中发现的情况相似。令人惊讶的是,IgH基因座仍然发生等位基因排斥,因此SL链似乎不参与等位基因排斥。

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