TGF-β-activated kinase 1 stimulates NF-κB activation by an NF-κB-inducing kinase-independsnt mechanism
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Sakurai, H
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Tanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, JapanTanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, Japan
Sakurai, H
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Shigemori, N
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Tanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, JapanTanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, Japan
Shigemori, N
[1
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Hasegawa, K
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Tanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, JapanTanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, Japan
Hasegawa, K
[1
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Sugita, T
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Tanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, JapanTanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, Japan
Sugita, T
[1
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[1] Tanabe Seiyaku Co Ltd, Lead Generat Res Lab, Yodogawa Ku, Osaka 5320031, Japan
Several mitogen-activated protein kinase kinase kinases (MAPKKKs), including NF-kappa B-inducing kinase (NIK), play critical roles in NF-kappa B activation, We isolated cDNA for human TGF-beta activated kinase 1 (TAK1), a member of the MAPKKK family, and evaluated its ability to stimulate NF-kappa B activation. Overexpression of TAK1 together with its activator protein, TAK1 binding protein 1 (TAB1), induced the nuclear translocation of NF-kappa B p50/p65 heterodimer accompanied by the degradation of I kappa B alpha and I kappa B beta, and the expression of kappa B-dependent reporter gene. A dominant negative mutant of NIK did not inhibit TAK1-induced NF-kappa B activation. These results suggest that TAK1 induces NF-kappa B activation through a novel NIK-independent signaling pathway. (C) 1998 Academic Press.
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Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Andreakos, E.
Williams, R. O.
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Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Williams, R. O.
Wales, J.
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Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Wales, J.
Foxwell, B. M.
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Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Foxwell, B. M.
Feldmann, M.
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Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandUniv London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
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Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USA
Russo, MP
Schwabe, RF
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Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USA
Schwabe, RF
Sartor, RB
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Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USA
Sartor, RB
Jobin, C
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Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USA