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B淋巴细胞中的负向信号传导可诱导145 kDa肌醇多磷酸5-磷酸酶SHIP发生酪氨酸磷酸化。

Negative signaling in B lymphocytes induces tyrosine phosphorylation of the 145-kDa inositol polyphosphate 5-phosphatase, SHIP.

作者信息

Chacko G W, Tridandapani S, Damen J E, Liu L, Krystal G, Coggeshall K M

机构信息

Department of Microbiology, Ohio State University, Columbus 43210, USA.

出版信息

J Immunol. 1996 Sep 15;157(6):2234-8.

PMID:8805618
Abstract

Stimulation of the B cell Ag receptor (BCR) has been reported to induce tyrosine phosphorylation of a 145-kDa protein and its association with the adapter protein Shc. We have identified this protein as the novel inositol polyphosphate 5-phosphatase (SHIP). Further analysis revealed that both maximal phosphorylation of SHIP and its association with Shc require co-clustering with the Fc receptor for IgG (Fc gamma RII) rather than stimulation of the BCR alone. Since co-clustering of the BCR and Fc gamma RII also down-regulates proliferation induced by Ag receptor stimulation, we hypothesize that tyrosine phosphorylation of SHIP and its association with Shc contribute to negative signaling through effects on inositol and phosphatidylinositol metabolism.

摘要

据报道,B细胞抗原受体(BCR)的刺激可诱导一种145 kDa蛋白的酪氨酸磷酸化及其与衔接蛋白Shc的结合。我们已将该蛋白鉴定为新型肌醇多磷酸5-磷酸酶(SHIP)。进一步分析表明,SHIP的最大磷酸化及其与Shc的结合都需要与IgG的Fc受体(FcγRII)共同聚集,而不是仅刺激BCR。由于BCR和FcγRII的共同聚集也会下调抗原受体刺激诱导的增殖,我们推测SHIP的酪氨酸磷酸化及其与Shc的结合通过对肌醇和磷脂酰肌醇代谢的影响而有助于负向信号传导。

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