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B 细胞对 B 细胞受体可变区的耐受性。

B-cell tolerance to the B-cell receptor variable regions.

机构信息

Centre for Immune Regulation, Institute of Immunology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

出版信息

Eur J Immunol. 2013 Oct;43(10):2577-87. doi: 10.1002/eji.201243203. Epub 2013 Jul 19.

Abstract

An enormous number of B cells with different B-cell receptors (BCRs) are continuously produced in the bone marrow. BCRs are further diversified during the germinal center reaction. Due to extensive recirculation, B cells with mutually binding BCR are likely to meet in lymphoid organs. We have addressed possible outcomes of such an encounter in vitro. B lymphoma cells were transfected with complementary BCR, one transfectant expressing an Idiotype⁺ (Id⁺) BCR and the other an anti-Id BCR. To exclude confounding effects of secreted Ig, the transfected B lymphoma cells only expressed membrane IgD. Coincubation of paired Id⁺/anti-Id lymphoma cells results in conjugate formation, signaling, activation of Caspase 3/7, and apoptosis of at least one of the two cells in the pair. Our data provide suggestive evidence for a mechanism whereby the B-cell compartment is partly purged of B cells with complementary BCRs.

摘要

大量具有不同 B 细胞受体 (BCR) 的 B 细胞在骨髓中不断产生。BCR 在生发中心反应中进一步多样化。由于广泛的再循环,具有相互结合的 BCR 的 B 细胞可能在淋巴器官中相遇。我们已经在体外研究了这种相遇的可能结果。用互补的 BCR 转染 B 淋巴瘤细胞,一种转染细胞表达同种型⁺(Id⁺)BCR,另一种转染细胞表达抗-Id BCR。为了排除分泌 Ig 的混杂影响,转染的 B 淋巴瘤细胞仅表达膜 IgD。配对的 Id⁺/抗-Id 淋巴瘤细胞的共孵育导致缀合物的形成、信号转导、Caspase 3/7 的激活以及至少一对细胞中的一个细胞的凋亡。我们的数据提供了暗示性的证据,表明 B 细胞亚群部分被具有互补 BCR 的 B 细胞清除。

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