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记忆 B 细胞和浆细胞分化的调控。

Regulation of memory B and plasma cell differentiation.

机构信息

Laboratory of Lymphocyte Differentiation, WPI Immunology Frontier Research Center, and Graduate School of Frontier Biosciences, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.

Laboratory of Lymphocyte Differentiation, WPI Immunology Frontier Research Center, and Graduate School of Frontier Biosciences, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan; Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences (IMS), Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.

出版信息

Curr Opin Immunol. 2017 Apr;45:126-131. doi: 10.1016/j.coi.2017.03.003. Epub 2017 Mar 27.

Abstract

Memory B cell generation and antibody production result from a differentiation process that begins when the surface BCR on naïve B cells binds an antigen. How the choice between these fates is tempo-spatially regulated is still obscure, but recent advances have reinforced the concept that the combination of B cell-intrinsic heterogeneity and -extrinsic heterogeneity provided by cells such as T cells is a key determinant. As molecular regulators, the transcription factors IRF4 and Bach2, which participate in these fate choices, have been emerging.

摘要

记忆 B 细胞的生成和抗体的产生源于一个分化过程,该过程始于初始 B 细胞表面的 BCR 与抗原结合。这些命运之间的选择如何在时空上受到调节仍然不清楚,但最近的进展加强了这样一种概念,即 B 细胞内在异质性和 T 细胞等细胞提供的外在异质性的组合是一个关键决定因素。作为分子调节剂,参与这些命运选择的转录因子 IRF4 和 Bach2 已经出现。

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