期刊
BIOCHEMICAL SOCIETY TRANSACTIONS
卷 31, 期 -, 页码 281-285出版社
PORTLAND PRESS
DOI: 10.1042/bst0310281
关键词
B-cell receptor; B-lymphocyte; Fc receptor; phosphatase; signal transduction
The inhibitory IgG receptor, FcgammaRIIB, blocks signalling by co-aggregated antigen receptors on mature and activated B-cells. FcgammaRIIB is also expressed by immature B-cells; however, its function on these cells has not been defined. in the present paper, we demonstrate that immature B-cells are highly sensitive to inhibitory signalling mediated by FcgammaRIIB. Co-aggregation of FcgammaRIIB with the B-cell antigen receptor (BCR) on immature B-cells leads to near ablation of late phase calcium mobilization. Concomitant with enhanced inhibitory signalling, we found that Src-homology-2-domain-containing inositol 5'-phosphatase (SHIP) is expressed at much higher levels in immature B-cells than in mature B-cells. Perhaps most importantly, we report that SHIP activated by BCR-FcgammaRIIB co-aggregation inhibits independently ligated receptors whose signalling requires PtdIns(3,4,5)P-3. We found that stromal-derived factor 1 (SDF-1)-induced cell migration is impaired by prior activation of FcgammaRIIB. This inhibition is reduced in SHIP-deficient B-cells. Therefore receptor-mediated signalling responses that are dependent on PtdIns(3,4,5)P-3 are subject to both direct and indirect inhibition by FcgammaRIIB-activated SHIP.
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