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MKP-7, a negative regulator of JNK, regulates VCAM-1 expression through IRF-1
Irina Tsoy Nizamutdinova1, Young Min Kim, Jae Heun Lee
1Department of Pharmacology, School of Medicine, Institute of Health Sciences, Gyeongsang National University, Jinju, Republic of Korea.
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.
Insights
JNK signaling negatively regulates vascular cell adhesion molecule-1 (VCAM-1) expression in endothelial cells. MKP-7, a JNK regulator, controls VCAM-1 via IRF-1, impacting atherosclerosis and tumor progression.
Area of Science:
- Molecular Biology
- Cell Biology
- Immunology
Background:
- Cell adhesion molecules (CAMs) like VCAM-1 and ICAM-1 are implicated in various pathologies, including cancer and atherosclerosis.
- VCAM-1, more than ICAM-1, is crucial for atherosclerosis initiation and tumor progression.
- Understanding the differential regulation of VCAM-1 and ICAM-1 is vital for therapeutic strategies.
Purpose of the Study:
- To elucidate the distinct regulatory mechanisms governing VCAM-1 and ICAM-1 expression.
- To investigate the role of JNK signaling in TNF-α-induced VCAM-1 and ICAM-1 expression.
- To determine the involvement of transcription factors IRF-1 and GATA6 in JNK-mediated VCAM-1 regulation.
Main Methods:
- Utilized specific JNK inhibitor (SP600125) and dominant-negative (DN) JNK1 plasmid.
- Employed JNK1-overexpressing vectors and MKP-7 silencing via siRNA.
- Performed chromatin immunoprecipitation (ChIP) assays to assess transcription factor binding to the VCAM-1 promoter.
Main Results:
- JNK inhibition enhanced TNF-α-induced VCAM-1 expression, while JNK overexpression inhibited it, indicating JNK's negative regulatory role.
- DN-JNK1 transfection increased IRF-1 binding to the VCAM-1 promoter, whereas JNK1 overexpression decreased it; GATA6 binding was unaffected.
- MKP-7 silencing increased JNK phosphorylation and inhibited VCAM-1 expression and IRF-1 binding, suggesting MKP-7 positively regulates VCAM-1 via JNK/IRF-1.
Conclusions:
- JNK signaling negatively regulates TNF-α-induced VCAM-1 expression in endothelial cells, primarily through modulation of IRF-1.
- MKP-7 acts as a positive regulator of VCAM-1 expression by deactivating JNK, influencing IRF-1 activity.
- These findings highlight a novel pathway (MKP-7/JNK/IRF-1) controlling VCAM-1, offering potential therapeutic targets for inflammatory diseases and cancer.
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