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Notch活性与B细胞受体及CD40信号协同作用,以增强B细胞活化。

Notch activity synergizes with B-cell-receptor and CD40 signaling to enhance B-cell activation.

作者信息

Thomas Matthew, Calamito Marco, Srivastava Bhaskar, Maillard Ivan, Pear Warren S, Allman David

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, 36th and Hamilton Walk, Philadelphia, PA 19104, USA.

出版信息

Blood. 2007 Apr 15;109(8):3342-50. doi: 10.1182/blood-2006-09-046698. Epub 2006 Dec 19.

Abstract

How diverse environmental cues are integrated to regulate B-cell activation and development remains poorly understood. Here we show that Notch activity synergizes with B-cell receptor (BCR) and/or CD40 signaling to enhance several aspects of B-cell activation and function. We find that costimulation of follicular B cells with the Notch ligand Delta-like-1 leads to significant increases in BCR- and CD40-mediated proliferation and enhances production of IgG1(+) cells in vitro and in vivo. We further find that coengagement of Notch and the BCR results in increased activation of the MAPK pathway, and MAPK and Notch inhibitors prevent B-cell activation events mediated by coengagement of Notch and the BCR. These data suggest that the BCR and CD40 signaling pathways collaborate with the Notch pathway to optimize B-cell activation.

摘要

目前对于多种环境信号如何整合以调节B细胞活化和发育仍知之甚少。在此,我们表明Notch活性与B细胞受体(BCR)和/或CD40信号协同作用,以增强B细胞活化和功能的多个方面。我们发现用Notch配体Delta样-1共刺激滤泡B细胞会导致BCR和CD40介导的增殖显著增加,并在体外和体内增强IgG1(+)细胞的产生。我们进一步发现Notch和BCR的共同结合导致MAPK途径的活化增加,并且MAPK和Notch抑制剂可阻止由Notch和BCR共同结合介导的B细胞活化事件。这些数据表明BCR和CD40信号通路与Notch通路协作以优化B细胞活化。

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