Nitschke Lars
Department of Genetics, University of Erlangen, Staudtstrasse 5, 91058 Erlangen, Germany.
Curr Opin Immunol. 2005 Jun;17(3):290-7. doi: 10.1016/j.coi.2005.03.005.
Inhibitory co-receptors downmodulate B-cell receptor (BCR) signalling by setting a signalling threshold that prevents overstimulation of B cells. Activation of these inhibitory co-receptors occurs by phosphorylation on their cytoplasmic inhibitory immunoreceptor tyrosine-based inhibition motifs (ITIMs), followed by recruitment of the tyrosine phosphatase SHP-1 or the lipid phosphatase SHIP, and depends on their association with the BCR. Recent evidence shows that B-cell signal inhibition is regulated by ligand binding of inhibitory receptors.
抑制性共受体通过设定一个防止B细胞过度刺激的信号阈值来下调B细胞受体(BCR)信号传导。这些抑制性共受体的激活是通过其细胞质抑制性免疫受体酪氨酸抑制基序(ITIM)上的磷酸化,随后募集酪氨酸磷酸酶SHP-1或脂质磷酸酶SHIP来实现的,并且依赖于它们与BCR的结合。最近的证据表明,B细胞信号抑制是由抑制性受体的配体结合所调节的。