Harris Stephanie J, Parry Richard V, Westwick John, Ward Stephen G
Inflammatory Cell Biology Laboratory, Department of Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom.
J Biol Chem. 2008 Feb 1;283(5):2465-9. doi: 10.1074/jbc.R700044200. Epub 2007 Dec 10.
The phosphoinositide 3-kinase signaling pathway has been implicated in a range of T lymphocyte cellular functions, particularly growth, proliferation, cytokine secretion, and survival. Dysregulation of phosphoinositide 3-kinase-dependent signaling and function in leukocytes, including B and T lymphocytes, has been implicated in many inflammatory and autoimmune diseases. As befits a pivotal signaling cascade, several mechanisms exist to ensure that the pathway is tightly regulated. This minireview focuses on two lipid phosphatases, viz. the 3'-phosphatase PTEN (phosphatase and tensin homolog deleted on chromosome 10) and SHIP (Src homology 2 domain-containing inositol-5-phosphatase). We discuss their role in regulating T lymphocyte signaling as well their potential as future therapeutic targets.
磷酸肌醇3-激酶信号通路与一系列T淋巴细胞的细胞功能有关,特别是生长、增殖、细胞因子分泌和存活。白细胞(包括B淋巴细胞和T淋巴细胞)中磷酸肌醇3-激酶依赖性信号传导和功能的失调与许多炎症和自身免疫性疾病有关。作为一个关键的信号级联反应,存在多种机制来确保该通路受到严格调控。本综述聚焦于两种脂质磷酸酶,即3'-磷酸酶PTEN(第10号染色体缺失的磷酸酶及张力蛋白同源物)和SHIP(含Src同源2结构域的肌醇-5-磷酸酶)。我们讨论它们在调节T淋巴细胞信号传导中的作用以及作为未来治疗靶点的潜力。