Melchers Fritz
Max Planck Institute for Infection Biology, Campus Charité Mitte, Schumannstrasse 21-22, D-10117 Berlin, Germany.
Nat Rev Immunol. 2005 Jul;5(7):578-84. doi: 10.1038/nri1649.
In this Opinion article, I address the role of the pre-B-cell receptor (pre-BCR) in the development of antigen-specific B cells in terms of immunoglobulin heavy chain (IgH) variable-region repertoire selection, precursor B-cell differentiation and proliferation, and IgH allelic exclusion. Comparisons with the role of the pre-T-cell receptor (pre-TCR) in T-cell development raise provocative questions. Why do B- and T-cell lineages both use a surrogate chain - the surrogate light chain and the pre-TCR alpha-chain, respectively - as a step to develop their repertoires of antigen-recognizing cells? What are the functions of the pre-BCR and pre-TCR in lymphocyte differentiation and antigen-receptor allelic exclusion? This article, together with the accompanying article by Harald von Boehmer, hopes to answer some of these questions.
在这篇观点文章中,我从免疫球蛋白重链(IgH)可变区库选择、前体B细胞分化与增殖以及IgH等位基因排斥等方面,探讨前B细胞受体(pre-BCR)在抗原特异性B细胞发育中的作用。与前T细胞受体(pre-TCR)在T细胞发育中的作用进行比较,引发了一些引人深思的问题。为什么B细胞和T细胞谱系都使用替代链——分别是替代轻链和pre-TCRα链——作为发展其抗原识别细胞库的一个步骤?pre-BCR和pre-TCR在淋巴细胞分化和抗原受体等位基因排斥中的功能是什么?本文与哈拉尔德·冯·伯默尔(Harald von Boehmer)撰写的随附文章,希望能回答其中的一些问题。