Fine tuning T lymphocytes: A role for the lipid phosphatase SHIP-1

The phosphoinositide 3-kinase signaling pathway regulates a range of T lymphocyte cellular functions including growth, proliferation, cytokine secretion and survival. Aberrant regulation of phosphoinositide 3-kinase-dependent signaling in T lymphocytes has been implicated in inflammatory and autoimm...

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Veröffentlicht in:Biochimica et biophysica acta 2010-03, Vol.1804 (3), p.592-597
Hauptverfasser: Parry, Richard V., Harris, Stephanie J., Ward, Stephen G.
Format: Artikel
Sprache:eng
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Zusammenfassung:The phosphoinositide 3-kinase signaling pathway regulates a range of T lymphocyte cellular functions including growth, proliferation, cytokine secretion and survival. Aberrant regulation of phosphoinositide 3-kinase-dependent signaling in T lymphocytes has been implicated in inflammatory and autoimmune diseases. In common with much of the immune system, several mechanisms exist to ensure the pathway is tightly regulated to elicit appropriate responses. One level of control involves the Src homology 2 domain-containing inositol-5-phosphatase-1 (SHIP-1) that modulates phosphoinositide 3-kinase signaling by degrading the key signaling lipid PI(3,4,5)P3 to PI(3,4)P2, but also serves as a key scaffolding molecule in the formation of multi-protein complexes. Here we discuss the role of SHIP-1 in regulating T lymphocyte and immune function, as well as its potential as a therapeutic target.
ISSN:1570-9639
0006-3002
1878-1454
DOI:10.1016/j.bbapap.2009.09.019