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人 B 细胞中抗 DNA 受体的轻链编辑器。

Light chain editors of anti-DNA receptors in human B cells.

机构信息

Gwen Knapp Center for Lupus and Immunology Research, Department of Pathology, University of Chicago, Chicago, IL 60637.

出版信息

J Exp Med. 2014 Feb 10;211(2):357-64. doi: 10.1084/jem.20122340. Epub 2014 Jan 27.

Abstract

Receptor editing is a mechanism of self-tolerance used in newly generated B cells. The expressed heavy (H) or light (L) chain of an autoreactive receptor is replaced by upstream V genes which eliminate or modify autoreactivity. Editing of anti-DNA receptors has been characterized in anti-DNA transgenic mouse models including 3H9, 3H9/56R, and their revertant 3H9GL. Certain L chains, termed editors, rescue anti-DNA B cells by neutralizing or modifying DNA binding of the H chain. This editing mechanism acts on the natural H chain repertoire; endogenous H chains with anti-DNA features are expressed primarily in combination with editor L chains. We ask whether a similar set of L chains exists in the human repertoire, and if so, do they edit H chains with anti-DNA signatures? We compared the protein sequences of mouse editors to all human L chains and found several human L chains similar to mouse editors. These L chains diminish or veto anti-DNA binding when expressed with anti-DNA H chains. The human H chains expressed with these L chains also have relatively high arginine (Arg) content in the H chain complementarity determining region (H3), suggesting that receptor editing plays a role in establishing tolerance to DNA in humans.

摘要

受体编辑是新生成的 B 细胞中用于自身耐受的机制。自身反应性受体表达的重(H)链或轻(L)链被上游 V 基因取代,从而消除或修饰自身反应性。在包括 3H9、3H9/56R 及其回复体 3H9GL 在内的抗 DNA 转基因小鼠模型中,已经对抗 DNA 受体的编辑进行了特征描述。某些 L 链,称为编辑体,通过中和或修饰 H 链与 DNA 的结合来拯救抗 DNA B 细胞。这种编辑机制作用于天然 H 链库;具有抗 DNA 特征的内源性 H 链主要与编辑体 L 链结合表达。我们想知道人类库中是否存在类似的 L 链集合,如果存在,它们是否编辑具有抗 DNA 特征的 H 链?我们比较了小鼠编辑体与所有人类 L 链的蛋白质序列,发现了一些与小鼠编辑体相似的人类 L 链。当与抗 DNA H 链表达时,这些 L 链会减少或否决抗 DNA 结合。与这些 L 链表达的人类 H 链在 H 链互补决定区(H3)中也具有相对较高的精氨酸(Arg)含量,这表明受体编辑在人类中建立对 DNA 的耐受中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a19/3920568/59dfdc015758/JEM_20122340_Fig1.jpg

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