20-Hydroxyeicosatetraenoic acid mediates calcium/calmodulin-dependent protein kinase II-induced mitogen-activated protein kinase activation in vascular smooth muscle cells
| العنوان: | 20-Hydroxyeicosatetraenoic acid mediates calcium/calmodulin-dependent protein kinase II-induced mitogen-activated protein kinase activation in vascular smooth muscle cells |
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| المؤلفون: | Kafait U. Malik, M. M. Muthalif, Jason L. Harper, Ibrahim F. Benter, Soghra Fatima, Mohammed R. Uddin, Nour A. Karzoun |
| المصدر: | Proceedings of the National Academy of Sciences. 95:12701-12706 |
| بيانات النشر: | Proceedings of the National Academy of Sciences, 1998. |
| سنة النشر: | 1998 |
| مصطلحات موضوعية: | Male, MAPK/ERK pathway, Vascular smooth muscle, Lipoxygenase, Biology, Muscle, Smooth, Vascular, Phospholipases A, chemistry.chemical_compound, Phospholipase A2, Cytochrome P-450 Enzyme System, Ca2+/calmodulin-dependent protein kinase, Hydroxyeicosatetraenoic Acids, Animals, Protein kinase A, Cells, Cultured, Arachidonic Acid, Multidisciplinary, Epidermal Growth Factor, Kinase, Angiotensin II, Biological Sciences, 20-Hydroxyeicosatetraenoic acid, Cell biology, Enzyme Activation, Phospholipases A2, chemistry, Calcium-Calmodulin-Dependent Protein Kinases, cardiovascular system, biology.protein, lipids (amino acids, peptides, and proteins), Rabbits, Calcium-Calmodulin-Dependent Protein Kinase Type 2 |
| الوصف: | Norepinephrine (NE) and angiotensin II (Ang II), by promoting extracellular Ca 2+ influx, increase Ca 2+ /calmodulin-dependent kinase II (CaMKII) activity, leading to activation of mitogen-activated protein kinase (MAPK) and cytosolic phospholipase A 2 (cPLA 2 ), resulting in release of arachidonic acid (AA) for prostacyclin synthesis in rabbit vascular smooth muscle cells. However, the mechanism by which CaMKII activates MAPK is unclear. The present study was conducted to determine the contribution of AA and its metabolites as possible mediators of CaMKII-induced MAPK activation by NE, Ang II, and epidermal growth factor (EGF) in vascular smooth muscle cells. NE-, Ang II-, and EGF-stimulated MAPK and cPLA 2 were reduced by inhibitors of cytochrome P450 (CYP450) and lipoxygenase but not by cyclooxygenase. NE-, Ang II-, and EGF-induced increases in Ras activity, measured by its translocation to plasma membrane, were abolished by CYP450, lipoxygenase, and farnesyltransferase inhibitors. An AA metabolite of CYP450, 20-hydroxyeicosatetraenoic acid (20-HETE), increased the activities of MAPK and cPLA 2 and caused translocation of Ras. These data suggest that activation of MAPK by NE, Ang II, and EGF is mediated by a signaling mechanism involving 20-HETE, which is generated by stimulation of cPLA 2 by CaMKII. Activation of Ras/MAPK by 20-HETE amplifies cPLA 2 activity and releases additional AA by a positive feedback mechanism. This mechanism of Ras/MAPK activation by 20-HETE may play a central role in the regulation of other cellular signaling molecules involved in cell proliferation and growth. |
| تدمد: | 1091-6490 0027-8424 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a938a64eb5b19f034541bf8837f1a1eTest https://doi.org/10.1073/pnas.95.21.12701Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....9a938a64eb5b19f034541bf8837f1a1e |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 10916490 00278424 |
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