The c-Jun NH2-terminal kinases (JNKs) are a group of mitogen-activated protein (MAP) kinases that participate in signal transduction events mediating specific cellular functions. Activation of JNK is regulated by phosphorylation in response to cellular stress and inflammatory cytokines. Here, we demonstrate that JNK is regulated by a second, novel mechanism. Induction of Jnk gene expression is required in specific tissues before activation of this signaling pathway. The in vivo and in vitro ligation of the T cell receptor (TCR) leads to induction of JNK gene and protein expression. TCR signals are sufficient to induce JNK expression, whereas JNK phosphorylation also requires CD28-mediated costimulatory signals. Therefore, both expression and activation contribute to the regulation of the JNK pathway to ensure proper control during the course of an immune response.
Skip Nav Destination
Article navigation
3 January 2000
Article|
January 03 2000
Regulation of c-Jun NH2-terminal Kinase ( Jnk) Gene Expression during T Cell Activation
Linda Weiss,
Linda Weiss
aImmunobiology Program, Department of Medicine, University of Vermont, Burlington, Vermont 05405
Search for other works by this author on:
Alan J. Whitmarsh,
Alan J. Whitmarsh
bHoward Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605
Search for other works by this author on:
Derek D. Yang,
Derek D. Yang
cSection of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06520
Search for other works by this author on:
Mercedes Rincón,
Mercedes Rincón
aImmunobiology Program, Department of Medicine, University of Vermont, Burlington, Vermont 05405
Search for other works by this author on:
Roger J. Davis,
Roger J. Davis
bHoward Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605
Search for other works by this author on:
Richard A. Flavell
Richard A. Flavell
cSection of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06520
Search for other works by this author on:
Linda Weiss
aImmunobiology Program, Department of Medicine, University of Vermont, Burlington, Vermont 05405
Alan J. Whitmarsh
bHoward Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605
Derek D. Yang
cSection of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06520
Mercedes Rincón
aImmunobiology Program, Department of Medicine, University of Vermont, Burlington, Vermont 05405
Roger J. Davis
bHoward Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605
Richard A. Flavell
cSection of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06520
D.D. Yang's present address is Lilly Research Laboratory, Eli Lilly and Co., Indianapolis, IN 46285.
Abbreviations used in this paper: AP-1, activator protein 1; ERK, extracellular signal–regulated kinase; GST, glutathione S-transferase; JNK, c-Jun NH2-terminal kinase; MAP, mitogen-activated protein; MKK, MAP kinase kinase; SAPK, stress-activated protein kinase; SEB, staphylococcal enterotoxin B.
Received:
July 07 1999
Revision Requested:
October 20 1999
Accepted:
October 22 1999
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Exp Med (2000) 191 (1): 139–146.
Article history
Received:
July 07 1999
Revision Requested:
October 20 1999
Accepted:
October 22 1999
Citation
Linda Weiss, Alan J. Whitmarsh, Derek D. Yang, Mercedes Rincón, Roger J. Davis, Richard A. Flavell; Regulation of c-Jun NH2-terminal Kinase ( Jnk) Gene Expression during T Cell Activation. J Exp Med 3 January 2000; 191 (1): 139–146. doi: https://doi.org/10.1084/jem.191.1.139
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement