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截短的免疫球蛋白重链蛋白Dmu对B淋巴细胞发育的调控

Regulation of B lymphocyte development by the truncated immunoglobulin heavy chain protein Dmu.

作者信息

Tornberg U C, Bergqvist I, Haury M, Holmberg D

机构信息

Department of Cell and Molecular Biology, Umeâ University, S-901 87 Umeâ, Sweden.

出版信息

J Exp Med. 1998 Mar 2;187(5):703-9. doi: 10.1084/jem.187.5.703.

Abstract

The development of B lymphocytes from progenitor cells is dependent on the expression of a pre-B cell-specific receptor made up by a mu heavy chain associated with the surrogate light chains, immunoglobulin (Ig)alpha, and Igbeta. A variant pre-B cell receptor can be formed in which the mu heavy chain is exchanged for a truncated mu chain denoted Dmu. To investigate the role of this receptor in the development of B cells, we have generated transgenic mice that express the Dmu protein in cells of the B lineage. Analysis of these mice reveal that Dmu expression leads to a partial block in B cell development at the early pre-B cell stage, probably by inhibiting VH to DHJH rearrangement. Furthermore, we provide evidence that Dmu induces VL to JL rearrangements.

摘要

B淋巴细胞从祖细胞发育而来依赖于前B细胞特异性受体的表达,该受体由与替代轻链、免疫球蛋白(Ig)α和Igβ相关的μ重链组成。可以形成一种变体前B细胞受体,其中μ重链被替换为截短的μ链,称为Dμ。为了研究该受体在B细胞发育中的作用,我们构建了在B系细胞中表达Dμ蛋白的转基因小鼠。对这些小鼠的分析表明,Dμ的表达可能通过抑制VH至DHJH重排导致早期前B细胞阶段B细胞发育的部分阻滞。此外,我们提供证据表明Dμ诱导VL至JL重排。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/733e/2212169/6b724dee35e1/JEM971599.f1.jpg

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