Inactivation of JNK activity by mitogen-activated protein kinase phosphatase-2 in EAhy926 endothelial cells is dependent upon agonist-specific JNK translocation to the nucleus

التفاصيل البيبلوغرافية
العنوان: Inactivation of JNK activity by mitogen-activated protein kinase phosphatase-2 in EAhy926 endothelial cells is dependent upon agonist-specific JNK translocation to the nucleus
المؤلفون: Caspar J. M. Robinson, Callum M. Sloss, Robin Plevin
المصدر: Cellular signalling. 13(1)
سنة النشر: 2001
مصطلحات موضوعية: p38 mitogen-activated protein kinases, Mitogen-activated protein kinase kinase, p38 Mitogen-Activated Protein Kinases, Substrate Specificity, Humans, Endothelium, Protein Phosphatase 2, Kinase activity, Phosphorylation, Protein kinase A, Cell Nucleus, MAP kinase kinase kinase, biology, Tumor Necrosis Factor-alpha, JNK Mitogen-Activated Protein Kinases, Cell Biology, Protein phosphatase 2, Hydrogen Peroxide, Molecular biology, Antibodies, Anti-Idiotypic, Protein Transport, Mitogen-activated protein kinase, MAP kinase phosphatase, biology.protein, Dual-Specificity Phosphatases, Mitogen-Activated Protein Kinase Phosphatases, Mitogen-Activated Protein Kinases, Protein Tyrosine Phosphatases
الوصف: We have investigated the termination of agonist-stimulated mitogen-activated protein (MAP) kinase activity in EAhy926 cells by MAP kinase phosphatase-2 (MKP-2). In cells expressing either wild-type (WT) or catalytically inactive (CI)-MKP-2, there was no significant differences in TNFalpha-stimulated JNK or p38 MAP kinase activity, however hydrogen peroxide (H2O2)-stimulated JNK activity was substantially reduced in WT-MKP-2 expressing clones and enhanced in cells expressing CI-MKP-2. Consistent with these findings, we observed substantial nuclear translocation of JNK occurred in response to H2O2 but not TNFalpha. Using a phosphospecific anti-JNK antibody, we found that TNFalpha-stimulated JNK activity was associated principally with the cytosol while in response to H2O2, JNK activity was found within the nucleus. These results show that the role of MKP-2 in terminating JNK activity is determined by the translocation of JNK to the nucleus, which is under agonist-specific regulation and not a universal cellular response to stimulation.
تدمد: 0898-6568
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d3474437a5975b889e6be2e580860f0
https://pubmed.ncbi.nlm.nih.gov/11257445
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....4d3474437a5975b889e6be2e580860f0
قاعدة البيانات: OpenAIRE