| Literature DB >> 18073217 |
Stephanie J Harris1, Richard V Parry, John Westwick, Stephen G Ward.
Abstract
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.Entities:
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Year: 2007 PMID: 18073217 DOI: 10.1074/jbc.R700044200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157