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Science 11 February 2000: Vol. 287. no. 5455, pp. 1049 - 1053 DOI: 10.1126/science.287.5455.1049
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Reports
Central Role for G Protein-Coupled Phosphoinositide 3-Kinase in Inflammation
Emilio Hirsch,
1*
Vladimir L. Katanaev,
2
Cecilia Garlanda,
3
Ornella Azzolino,
1
Luciano Pirola,
2
Lorenzo Silengo,
1
Silvano Sozzani,
3
Alberto Mantovani,
34
Fiorella Altruda,
1
Matthias P. Wymann
2*
Phosphoinositide 3-kinase (PI3K) activity is crucial for
leukocyte function, but the roles of the four receptor-activated isoforms are unclear. Mice lacking heterotrimeric guanine
nucleotide-binding protein (G protein)-coupled PI3K were
viable and had fully differentiated neutrophils and macrophages.
Chemoattractant-stimulated PI3K / neutrophils did not
produce phosphatidylinositol 3,4,5-trisphosphate, did not activate
protein kinase B, and displayed impaired respiratory burst and
motility. Peritoneal PI3K -null macrophages showed a reduced
migration toward a wide range of chemotactic stimuli and a severely
defective accumulation in a septic peritonitis model. These results
demonstrate that PI3K is a crucial signaling molecule required for
macrophage accumulation in inflammation.
1 Department of Genetics, Biology and
Biochemistry, University of Torino, Turin, Italy.
2 Institute of Biochemistry, University of Fribourg,
CH-1700 Fribourg, Switzerland.
3 Istituto di
Ricerche Farmacologiche Mario Negri, Milan, Italy.
4 Section of General Pathology, University of
Brescia, Brescia, Italy.
*
To whom correspondence should be addressed. E-mail:
hirsch{at}molinette.unito.it and matthiaspaul.wymann{at}unifr.ch
These authors contributed equally to this work.
Read the Full Text
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- Phospholipase C, calcium, and calmodulin are critical for {alpha}4{beta}1 integrin affinity up-regulation and monocyte arrest triggered by chemoattractants.
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- Phosphoinositide 3-kinase {gamma}/{delta} inhibition limits infarct size after myocardial ischemia/reperfusion injury.
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PNAS
103, 19866-19871
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- Leukocyte phosphoinositide-3 kinase {gamma} is required for chemokine-induced, sustained adhesion under flow in vivo.
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80, 1491-1499
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FASEB J
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- Continuous signaling via PI3K isoforms beta and {gamma} is required for platelet ADP receptor function in dynamic thrombus stabilization.
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Blood
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- Regulation of epidermal homeostasis and repair by phosphoinositide 3-kinase.
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- DOCK2 regulates chemokine-triggered lateral lymphocyte motility but not transendothelial migration.
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- Neutrophil Signaling Pathways Activated by Bacterial DNA Stimulation.
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- To stabilize neutrophil polarity, PIP3 and Cdc42 augment RhoA activity at the back as well as signals at the front.
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- Class IA Phosphatidylinositide 3-Kinases, rather than p110{gamma}, Regulate Formyl-Methionyl-Leucyl-Phenylalanine-Stimulated Chemotaxis and Superoxide Production in Differentiated Neutrophil-Like PLB-985 Cells..
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- Phosphatidylinositol 3-Kinase {gamma} Signaling through Protein Kinase C{zeta} Induces NADPH Oxidase-mediated Oxidant Generation and NF-{kappa}B Activation in Endothelial Cells.
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- Characterization of p87PIKAP, a Novel Regulatory Subunit of Phosphoinositide 3-Kinase {gamma} That Is Highly Expressed in Heart and Interacts with PDE3B.
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