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布鲁顿酪氨酸激酶通过调节钙和钙调蛋白介导 TLR9 和 B 细胞受体之间的协同信号转导。

Bruton's tyrosine kinase mediates the synergistic signalling between TLR9 and the B cell receptor by regulating calcium and calmodulin.

机构信息

Immunology Research Centre, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.

出版信息

PLoS One. 2013 Aug 14;8(8):e74103. doi: 10.1371/journal.pone.0074103. eCollection 2013.

Abstract

B cells signal through both the B cell receptor (BCR) which binds antigens and Toll-like receptors (TLRs) including TLR9 which recognises CpG DNA. Activation of TLR9 synergises with BCR signalling when the BCR and TLR9 co-localise within an auto-phagosome-like compartment. Here we report that Bruton's tyrosine kinase (BTK) is required for synergistic IL6 production and up-regulation of surface expression of MHC-class-II, CD69 and CD86 in primary murine and human B cells. We show that BTK is essential for co-localisation of the BCR and TLR9 within a potential auto-phagosome-like compartment in the Namalwa human B cell line. Downstream of BTK we find that calcium acting via calmodulin is required for this process. These data provide new insights into the role of BTK, an important target for autoimmune diseases, in B cell activation.

摘要

B 细胞通过 B 细胞受体 (BCR) 结合抗原和 Toll 样受体 (TLR) 信号转导,其中 TLR9 识别 CpG DNA。当 BCR 和 TLR9 在自噬体样隔室内共定位时,TLR9 的激活与 BCR 信号协同作用。在这里,我们报告 Bruton 酪氨酸激酶 (BTK) 是协同产生白细胞介素 6 (IL6) 和上调主要小鼠和人 B 细胞表面 MHC 类 II、CD69 和 CD86 表达所必需的。我们表明 BTK 对于 Namalwa 人 B 细胞系中 BCR 和 TLR9 在潜在自噬体样隔室内的共定位是必需的。在 BTK 下游,我们发现钙通过钙调蛋白起作用是该过程所必需的。这些数据为 BTK(自身免疫性疾病的重要靶点)在 B 细胞激活中的作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c0/3743783/bde6278ed3cd/pone.0074103.g001.jpg

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