Ca2+ signaling in antigen receptor-activated B lymphocytes

被引:66
作者
Engelke, Michael
Engels, Niklas
Dittmann, Kai
Stork, Bjorn
Wienands, Jurgen
机构
[1] Univ Gottingen, Inst Cellular & Mol Immunol, D-37073 Gottingen, Germany
[2] Univ Tubingen, Dept Internal Med 1, D-72076 Tubingen, Germany
关键词
B-cell antigen receptor; protein tyrosine phosphorylation; adapter proteins; Ca2+ channels; intracellular protein localization;
D O I
10.1111/j.1600-065X.2007.00539.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cells respond to antigen stimulation with mobilization of the Ca2+ second messenger in two phases operated by two distinct sets of effector proteins. First, an antigen receptor-specific Ca2+ initiation complex is assembled, activated, and targeted to the plasma membrane to trigger the transient release of Ca2+ from intracellular stores of the endoplasmic reticulum. Second, more ubiquitously expressed Ca2+ channels of the plasma membrane are opened to allow for sustained Ca2+ influx from the extracellular medium. Depending on the developmental stage of the B cell, the kinetics and profile of the two phases are adjusted at multiple levels of positive and negative regulation. A molecular basis for the Ca2+ signaling plasticity is provided by cytosolic and transmembrane adapter proteins. They act as signal organizers, which control enzyme/substrate interactions by directing the different signaling modules into specific subcellular compartments. These arrangements orchestrate a graduated activation of Ca2+-sensitive downstream pathways, which ultimately determine appropriate cellular responses, namely elimination of autoreactive B cells or proliferation and differentiation of immunocompetent B cells into antibody-secreting plasma cells.
引用
收藏
页码:235 / 246
页数:12
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