Isoform-specific functions of phosphoinositide 3-kinases:: p110δ but not p110γ promotes optimal allergic responses in vivo
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Ali, Khaled
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Queen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, EnglandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Ali, Khaled
[1
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Camps, Montserrat
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Camps, Montserrat
[2
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Pearce, Wayne P.
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Queen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, EnglandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Pearce, Wayne P.
[1
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Ji, Hong
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Ji, Hong
[2
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Rueckle, Thomas
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Rueckle, Thomas
[2
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Kuehn, Nicolas
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Frimorfo, Fribourg, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Kuehn, Nicolas
[3
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Pasquali, Christian
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Pasquali, Christian
[2
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Chabert, Christian
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Chabert, Christian
[2
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Rommel, Christian
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Merck Serono Int, Geneva Res Ctr, Geneva, SwitzerlandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Rommel, Christian
[2
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Vanhaesebroeck, Bart
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Queen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, EnglandQueen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
Vanhaesebroeck, Bart
[1
]
机构:
[1] Queen Mary Univ London, Sir John Vane Res Ctr, Inst Canc, Ctr Cell Signaling, London EC1M 6BQ, England
[2] Merck Serono Int, Geneva Res Ctr, Geneva, Switzerland
The leukocyte-enriched p110 gamma and p110 delta isoforms of PI3K have been shown to control in vitro degranulation of mast cells induced by cross-linking of the high affinity receptor of IgE (Fc epsilon RI). However, the relative contribution of these PI3K isoforms in IgE-dependent allergic responses in vivo is controversial. A side-by-side comparative analysis of the role of p110 gamma and p110 delta in mast cell function, using genetic approaches and newly developed isoform-selective pharmacologic inhibitors, confirms that both PI3K isoforms play an important role in Fc epsilon RI-activated mast cell degranulation in vitro. In vivo, however, only p110 delta was found to be required for optimal IgE/Ag-dependent hypersensitivity responses in mice. These observations identify p110 delta as a key therapeutic target among PI3K isoforms for allergy- and mast cell-related diseases.