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MKP-7, a negative regulator of JNK, regulates VCAM-1 expression through IRF-1.
- Source :
-
Cellular signalling [Cell Signal] 2012 Apr; Vol. 24 (4), pp. 866-72. Date of Electronic Publication: 2011 Dec 13. - Publication Year :
- 2012
-
Abstract
- Cell adhesion molecules (CAMs) are involved in a variety of pathologies including cancer, inflammation, pathogenic infections and autoimmune disease. In particular, VCAM-1, rather than ICAM-1, plays a major role in the initiation of atherosclerosis and tumor progression. Therefore, we attempted to elucidate differential mechanisms that regulate VCAM-1 and ICAM-1 expressions. Down-regulation of JNK by a specific inhibitor (SP600125) or dominant negative (DN) JNK1 plasmid enhanced TNF-α-induced VCAM-1 but not ICAM-1 expression. Moreover, transfection with a JNK1-overexpressing vector resulted in the inhibition of VCAM-1 expression stimulated by TNF-α in HUVECs, suggesting that JNK negatively regulates TNF-α-induced VCAM-1 expression in endothelial cells (ECs). Next, we investigated whether JNK signaling affects IRF-1 and/or GATA6, which are transcription factors that mediate TNF-α induction of VCAM-1 but not ICAM-1. The DN-JNK1 plasmid-transfected cells enhanced TNF-α up-regulation of IRF-1 whereas JNK1-overexpressing cells displayed down-regulation; however, neither DN-JNK1 transfection nor JNK1 overexpression affected GATA6 protein levels in the nuclear fraction. Chromatin immunoprecipitation (ChIP) assay confirmed that the inhibition of JNK by DN-JNK1 transfection increases the binding of IRF-1 to the VCAM-1 promoter whereas the overexpression of JNK1 inhibits IRF-1 binding to the VCAM-1 promoter. However, neither DN-JNK1 nor JNK1 overexpression altered GATA6 affinity for the VCAM-1 promoter region. We also examined whether MKP-7 affects ICAM-1 or VCAM-1 by regulating JNK. TNF-α-induced phosphor-JNK levels increased after 5min, peaked at 10 min, and decreased after 30 min. Interestingly, MKP-7 protein levels increased after 30 min, when phosphor-JNK induction by TNF-α was decreased. In addition, silencing MKP-7 with specific siRNA resulted in an increase in phosphor-JNK and inhibited the expression of VCAM-1 but not ICAM-1. Moreover, silencing MKP-7 caused the down-regulation of IRF-1 protein levels and binding to the VCAM-1 promoter. Thus, we suggest that MKP-7, a negative regulator of JNK, regulates VCAM-1 expression in activated endothelial cells through IRF-1 but not GATA6.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Subjects :
- Chromatin Immunoprecipitation
Dual-Specificity Phosphatases genetics
GATA6 Transcription Factor genetics
GATA6 Transcription Factor metabolism
Genes, Reporter
Human Umbilical Vein Endothelial Cells
Humans
Interferon Regulatory Factor-1 genetics
Interferon Regulatory Factor-1 metabolism
Luciferases
MAP Kinase Kinase 4 antagonists & inhibitors
MAP Kinase Kinase 4 genetics
Mitogen-Activated Protein Kinase Phosphatases genetics
Plasmids
Protein Kinase Inhibitors pharmacology
Transfection
Tumor Necrosis Factor-alpha genetics
Tumor Necrosis Factor-alpha metabolism
Vascular Cell Adhesion Molecule-1 genetics
Dual-Specificity Phosphatases metabolism
Gene Expression Regulation
MAP Kinase Kinase 4 metabolism
Mitogen-Activated Protein Kinase Phosphatases metabolism
Signal Transduction genetics
Vascular Cell Adhesion Molecule-1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3913
- Volume :
- 24
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cellular signalling
- Publication Type :
- Academic Journal
- Accession number :
- 22182512
- Full Text :
- https://doi.org/10.1016/j.cellsig.2011.12.002