Inhibitor and activator: dual functions for SHIP in immunity and cancer

被引:85
|
作者
Kerr, William G. [1 ]
机构
[1] SUNY Upstate Med Univ, Syracuse, NY 13210 USA
来源
YEAR IN IMMUNOLOGY | 2011年 / 1217卷
关键词
SHIP; PI(3,4,5)P-3; PI(3,4)P-2; T-reg cells; NK cells; MIR cells; antigen presentation; osteoblasts; s-SHIP; cancer; Crohn's Disease; HSC; INOSITOL PHOSPHATASE SHIP; CELL-DEVELOPMENT; DEFICIENT MICE; TYROSINE PHOSPHORYLATION; ALLERGIC INFLAMMATION; TARGETED DISRUPTION; NEGATIVE REGULATION; LIPID PHOSPHATASE; TUMOR-SUPPRESSOR; REGULATORY CELLS;
D O I
10.1111/j.1749-6632.2010.05869.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
SHIP1 is at the nexus of intracellular signaling pathways in immune cells that mediate bone marrow (BM) graft rejection, production of inflammatory and immunosuppressive cytokines, immunoregulatory cell formation, the BM niche that supports development of the immune system, and immune cancers. This review summarizes how SHIP participates in normal immune physiology or the pathologies that result when SHIP is mutated. This review also proposes that SHIP can have either inhibitory or activating roles in cell signaling that are determined by whether signaling pathways distal to PI3K are promoted by SHIP's substrate (PI(3,4,5)P-3) or its product (PI(3,4)P-2). This review also proposes the "two PIP hypothesis" that postulates that both SHIP's product and its substrate are necessary for a cancer cell to achieve and sustain a malignant state. Finally, due to the recent discovery of small molecule antagonists and agonists for SHIP, this review discusses potential therapeutic settings where chemical modulation of SHIP might be of benefit.
引用
收藏
页码:1 / 17
页数:17
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