Cell Biochemistry and Function · 2004 · 23 citations · 36 references
BiologyBiosynthesisSignal TransductionCellular EnzymologyBiochemistryParasitic ProtozoaMedicineNatural SciencesVisceral LeishmaniasisLeishmania AmazonensisCellular BiochemistryPka MoleculeCell BiologyCell SignalingCellular PhysiologyProtein PhosphorylationPka Activity
Because of the importance of cell signalling processes in proliferation and differentiation, the adenylate cyclase pathway was studied, specifically the protein kinase A (PKA) in Leishmania amazonensis. The PKAs of soluble (SF) and enriched membrane fractions (MF) from infective/non-infective promastigotes and axenic amastigotes were assayed. In order to purify the PKA molecule, fractions were chromatographed on DEAE-cellulose columns and the phosphorylative activity was evaluated using [gamma(32)P]-ATP as the phosphate source. These experiments were performed in the presence of cyclic adenosine monophosphate (cAMP) and an inhibitor of PKA. Our data demonstrated that the PKA activity was significantly higher (about two times) in SF from promastigotes with a high concentration of metacyclic forms, when compared with the non-infective promastigotes, suggesting an association of this activity and the metacyclogenesis process. A discrete phosphorylative activity in axenic amastigotes was observed. As the adenylate cyclase/cAMP pathway would be involved in the parasite-host interiorization, the PKA activity may constitute a good intracellular target for studies of leishmanicidal drugs.
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Michael Steward · Immunology · 1983 · 325 citations · Full text
Haesun A. Kim, Jeffrey E. DeClue, Nancy Ratner · Journal of Neuroscience Research · 1997 · 106 citations · Full text
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Identification and regulation of protein kinase C-delta in human neutrophils
Jonathan Kent, Susan Sergeant, David J. Burns et al. · The Journal of Immunology · 1996 · 90 citations · Full text