Mitogen-activated protein (MAP) kinase cascades are signal transduction pathways that play pivotal regulatory roles in the biosynthesis of proinflammatory cyrokines. MAP kinase phosphatase (MKP)-1, an archetypal member of the MKP family, is essential for the dephosphorylation/deactivation of MAP kinases p38 and INK Earlier studies conducted using cultured immortalized macrophages provided compelling evidence indicating that MKP-1 deactivates p38 and JNK, thereby limiting pro-inflammatory cytokine biosynthesis in innate immune cells exposed to microbial components. Recent studies employing MKP-1 knockout mice have confirmed the central function of MKP-1 in the feedback control of p38 and JNK activity as well as the crucial physiological function of MKP-1 as a negative regulator of the synthesis of pro-inflammatory cytokines in vivo. MKP-1 was shown to be a major feedback regulator of the innate immune response and to play a critical role in preventing septic shock and multi-organ dysfunction during pathogenic infection. In this review, we will update the studies on the biochemical properties and the regulation of MKP-1, and summarize our understanding on the physiological function of this key phosphatase in the innate immune response. (c) 2007 Elsevier Inc. All rights reserved.
机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Abraham, Sonya M.
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Lawrence, Toby
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Lawrence, Toby
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Kleiman, Anna
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Kleiman, Anna
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Warden, Paul
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Warden, Paul
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Medghalchi, Mino
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Medghalchi, Mino
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Tuckermann, Jan
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Tuckermann, Jan
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Saklatvala, Jeremy
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Saklatvala, Jeremy
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Clark, Andrew R.
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Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
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Univ Texas, SW Med Ctr, Dept Internal Med, Howard Hughes Med Inst, Dallas, TX 75235 USAUniv Texas, SW Med Ctr, Dept Internal Med, Howard Hughes Med Inst, Dallas, TX 75235 USA
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Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France
Brondello, JM
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Pouysségur, J
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Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France
Pouysségur, J
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McKenzie, FR
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Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France
机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Abraham, Sonya M.
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Lawrence, Toby
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Lawrence, Toby
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Kleiman, Anna
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Kleiman, Anna
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Warden, Paul
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Warden, Paul
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Medghalchi, Mino
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Medghalchi, Mino
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Tuckermann, Jan
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Tuckermann, Jan
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Saklatvala, Jeremy
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机构:Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Saklatvala, Jeremy
;
Clark, Andrew R.
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Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
机构:
Univ Texas, SW Med Ctr, Dept Internal Med, Howard Hughes Med Inst, Dallas, TX 75235 USAUniv Texas, SW Med Ctr, Dept Internal Med, Howard Hughes Med Inst, Dallas, TX 75235 USA
机构:
Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France
Brondello, JM
;
Pouysségur, J
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Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France
Pouysségur, J
;
McKenzie, FR
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Ctr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, FranceCtr Antoine Lacassagne, CNRS, UMR 6543, Inst Signaling Dev Biol & Canc Res, F-06189 Nice, France