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免疫小鼠淋巴结生发中心中表达重组激活基因的B细胞的特征分析。

Characterization of B cells expressing recombination activating genes in germinal centers of immunized mouse lymph nodes.

作者信息

Hikida M, Mori M, Kawabata T, Takai T, Ohmori H

机构信息

Department of Biotechnology, Faculty of Engineering, Okayama University, Japan.

出版信息

J Immunol. 1997 Mar 15;158(6):2509-12.

PMID:9058779
Abstract

Products of recombination activating genes (RAG-1 and RAG-2) involved in the rearrangement of Ig genes have been shown to be expressed only in immature stages of B cells. However, we have recently found that RAG genes were re-expressed in mature mouse B cells activated in vitro and in germinal centers (GCs) of immunized mouse lymph nodes (LNs). Here, we report that RAG transcripts and their proteins were expressed in parallel with the formation of GCs in popliteal LNs from mice immunized in the hind footpads. Immunocytochemical analysis revealed that RAG+ B cells were localized within GCs and were present as apoptotic tingible body cells. RAG expression is not considered a nonspecific result of apoptosis, since apoptotic B cells generated by surface Ig-engagement did not express RAG genes. These results suggest a novel role of RAG products in the differentiation of B cells in GCs.

摘要

参与免疫球蛋白基因重排的重组激活基因(RAG-1和RAG-2)的产物已被证明仅在B细胞的未成熟阶段表达。然而,我们最近发现,RAG基因在体外激活的成熟小鼠B细胞以及免疫小鼠淋巴结(LN)的生发中心(GC)中重新表达。在此,我们报告,在经后足垫免疫的小鼠腘窝淋巴结中,RAG转录本及其蛋白的表达与GC的形成平行。免疫细胞化学分析显示RAG+B细胞定位于GC内,并以凋亡的可染小体细胞形式存在。RAG表达不被认为是凋亡的非特异性结果,因为通过表面免疫球蛋白结合产生的凋亡B细胞不表达RAG基因。这些结果提示RAG产物在GC中B细胞分化中具有新作用。

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