Mitogenic signaling by cyclic adenosine monophosphate in chromaffin cells involves phosphatidylinositol 3-kinase activation
| Autor: | James F. Powers, Suniti Misra, Arthur S. Tischler, Kimberly Schelling, Lyuba Varticovski |
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| Rok vydání: | 2001 |
| Předmět: |
Chromaffin Cells
Immunoblotting Protein Serine-Threonine Kinases Biology PC12 Cells Biochemistry Phosphatidylinositol 3-Kinases chemistry.chemical_compound Proto-Oncogene Proteins Cyclic AMP medicine Animals Cyclic adenosine monophosphate Phosphatidylinositol Enzyme Inhibitors Phosphorylation Phosphotyrosine Molecular Biology Protein kinase B Phosphoinositide-3 Kinase Inhibitors ADCY6 Kinase Cell Biology ADCY3 Rats Inbred F344 Rats Cell biology Enzyme Activation medicine.anatomical_structure chemistry Chromaffin cell Female Adrenal medulla Proto-Oncogene Proteins c-akt Cell Division |
| Zdroj: | Journal of Cellular Biochemistry. 81:89-98 |
| ISSN: | 1097-4644 0730-2312 |
| DOI: | 10.1002/jcb.1087 |
| Popis: | Increase of intracellular cyclic adenosine monophosphate by the permeant cyclic adenosine monophosphate analog, 8-(4-chlorophenylthio)-adenosine 3′:5′- cyclic monophosphate, is mitogenic for normal adult rat chromaffin cells. The mitogenic effect is blocked by the phosphatidylinositol 3-kinase inhibitor, LY294002, and is associated with accumulation of phosphorylated Akt and p70S6 kinase, suggesting that cyclic adenosine monophosphate activates Type l phosphatidylinositol 3-kinase. The mechanism of activation was examined in PC12 pheochromocytoma cells, which are neoplastic chromaffin cells that exhibit many of the biochemical characteristics of their normal counterparts. Incubation of PC12 cells with 8-(4-chlorophenylthio)-adenosine 3′:5′- cyclic monophosphate led to a significant increase in total phosphatidylinositol 3-kinase activity that was sensitive to low concentrations of LY294002. The increase was maximal at 1 h and returned to basal levels within six hours. Immunoprecipitation studies showed no increase in phosphatidylinositol 3-kinase activity in anti-phosphotyrosine immune complexes from PC12 cells stimulated by 8-(4-chlorophenylthio)-adenosine 3′:5′- cyclic monophosphate, in contrast to cells stimulated by nerve growth factor. Instead, activity was demonstrated in association with p110γ and p85. These findings suggest that cyclic adenosine monophosphate causes activation of Types IA and IB phosphatidylinositol 3-kinase by a novel mechanism in chromaffin and pheochromocytoma cells. That activation may contribute to chromaffin cell pro- liferation and to the development and progression of pheochromocytomas. J. Cell. Biochem. Suppl. 36: 89–98, 2001. © 2001 Wiley-Liss, Inc. |
| Databáze: | OpenAIRE |
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