Negative Feedback Regulation of Antigen Receptors through Calmodulin Inhibition of E2A

被引:7
作者
Verma-Gaur, Jiyoti [1 ]
Hauser, Jannek [1 ]
Grundstrom, Thomas [1 ]
机构
[1] Umea Univ, Dept Mol Biol, SE-90187 Umea, Sweden
基金
瑞典研究理事会;
关键词
B-CELL DEVELOPMENT; PROXIMITY LIGATION; IN-SITU; CALCIUM/CALMODULIN INHIBITION; GERMINAL-CENTER; E-PROTEINS; DIFFERENTIATION; BETA;
D O I
10.4049/jimmunol.1103105
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signaling from the BCR is used to judge Ag-binding strengths of the Abs of B cells. BCR signaling enables the selection for successive improvements in the Ag affinity over an extremely broad range of affinities during somatic hypermutation. We show that the mouse BCR is subject to general negative feedback regulation of the receptor proteins, as well as many coreceptors and proteins in signal pathways from the receptor. Thus, the BCR can downregulate itself, which can enable sensitive detection of successive improvements in the Ag affinity over a very large span of affinities. Furthermore, the feedback inhibition of the BCR signalosome and most of its proteins, as well as most other regulations of genes by BCR stimulation, is to a large extent through inhibition of the transcription factor E2A by Ca2+/calmodulin. The Journal of Immunology, 2012, 188: 6175-6183.
引用
收藏
页码:6175 / 6183
页数:9
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