Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Nat Immunol. 2019 Aug;20(8):963-969. doi: 10.1038/s41590-019-0427-9. Epub 2019 Jul 8.
Over the past several decades, B cell antigen receptor (BCR)-induced signaling pathways have been described in extraordinary molecular detail, mainly from studies of B cell responses to antigens in vitro. BCR signaling has been shown to govern the initiation of transcriptional programs associated with B cell activation and fate decisions, as well as the BCR-dependent processing of antigen and presentation of antigen to T cells. However, although the potential of the BCR to orchestrate B cell behavior was known, there was no clear appreciation of the context in which B cells signal in secondary lymphoid organs in vivo or how that context influences signaling. In this Review, we describe the current view of the cellular consequences of BCR signaling and advances in the understanding of B cell signaling in context in vivo.
在过去的几十年中,B 细胞抗原受体 (BCR) 诱导的信号通路已经在分子水平上被详细描述,主要来自于对 B 细胞体外对抗原反应的研究。BCR 信号已被证明可以控制与 B 细胞激活和命运决定相关的转录程序的启动,以及 BCR 依赖性抗原处理和抗原呈递给 T 细胞。然而,尽管 BCR 有协调 B 细胞行为的潜力,但人们并不清楚 B 细胞在体内次级淋巴器官中信号传递的背景,也不知道这种背景如何影响信号传递。在这篇综述中,我们描述了 BCR 信号传递的细胞后果的最新观点,以及对体内背景下 B 细胞信号传递的理解的进展。
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