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1.
Mol Biochem Parasitol ; 88(1-2): 25-33, 1997 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9274864

RESUMO

This study examines the changes in cellular lipids that take place when Trypanosoma cruzi epimastigotes and metacyclic trypomastigotes are transferred from 28 to 37 degrees C. We found a rise in the sterol to phospholipid ratio, as well as in the triacylglycerol and steryl ester cellular content in T. cruzi epimastigotes. In addition, saturated to unsaturated fatty acid ratios in phospholipids increase. This latter effect appears to be due to two concurrent processes. Firstly, fatty acyl delta9 and, especially, delta12 desaturations are significantly diminished at 37 degrees C. Secondly, triacylglycerols and steryl esters undergo changes in their fatty acyl composition opposite to those simultaneously observed in phospholipids, i.e. the ratio of saturated to unsaturated fatty acids markedly decreases. Similar alterations in each of the lipid classes and in the fatty acid composition of polar and neutral lipids were found in cultured metacyclic trypomastigotes on exposure to the same shift-up. These observations suggest that a global remodeling of cellular lipids that involves extensive fatty acid exchange between neutral and polar lipid pools represents a novel and important mechanism of adaptation of the parasites to the temperature changes they encounter in their life cycle.


Assuntos
Metabolismo dos Lipídeos , Trypanosoma cruzi/metabolismo , Adaptação Fisiológica , Animais , Ácidos Graxos Dessaturases/metabolismo , Ácidos Graxos/análise , Lipídeos/química , Fosfolipídeos/química , Fosfolipídeos/metabolismo , Esteróis/química , Esteróis/metabolismo , Temperatura , Triglicerídeos/química , Triglicerídeos/metabolismo , Trypanosoma cruzi/crescimento & desenvolvimento
2.
Biochem J ; 315 ( Pt 2): 513-6, 1996 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-8615822

RESUMO

We examined the role of protein kinase C alpha (PKC alpha ) in the stimulation of DNA synthesis of Swiss 3T3 cells induced by bombesin, platelet-derived growth factor (PDGF) and phorbol 12-myristate 13-acetate (PMA). We found that cells in which this kinase had been down-regulated showed a partially abrogated mitogenic response to bombesin. The response to PDGF was unaltered; however, the response to PMA was completely suppressed. The mitogenic effect of maximal doses of bombesin and PMA combined was greater than that of either agent alone, suggesting that bombesin does not fully activate the PKC pathway. Accordingly, bombesin-induced PKC alpha translocation from cytosol to membranes was partial, while that observed with PMA was essentially complete. Moreover, exposure to Ro-31-8220, a PKC inhibitor, had significantly greater effects on the response to PMA than on that to bombesin. Our findings point out different roles that PKC alpha may play in diversely activated cells: while, in the case of PMA, stimulation of this kinase may be necessary and sufficient to induce proliferation, it appears to be necessary only for a full response to bombesin, and redundant among the mechanisms triggered by PDGF.


Assuntos
Divisão Celular/fisiologia , Isoenzimas/fisiologia , Proteína Quinase C/fisiologia , Células 3T3 , Animais , Transporte Biológico Ativo/efeitos dos fármacos , Bombesina/farmacologia , Divisão Celular/efeitos dos fármacos , DNA/biossíntese , Regulação para Baixo , Interações Medicamentosas , Ativação Enzimática/efeitos dos fármacos , Camundongos , Mitógenos/farmacologia , Fator de Crescimento Derivado de Plaquetas/farmacologia , Proteína Quinase C-alfa , Acetato de Tetradecanoilforbol/farmacologia
3.
Biochem Biophys Res Commun ; 216(1): 348-54, 1995 Nov 02.
Artigo em Inglês | MEDLINE | ID: mdl-7488111

RESUMO

Coelenterates produce potent hemolysins inhibited by sphingomyelin (SM). Remarkably, instead of this lipid, their membranes contain a phosphono analogue of it. Using coelenterolysin (CL), a toxin produced by the sea anemone Phymactis clematis, we have examined a possible connection between these two peculiar traits. Our experiments showed that, while SM binds this lysin and inhibits its hemolytic activity, the endogenous PnSL do neither. In addition, liposomes made of bovine erythrocyte lipids are rapidly disrupted by CL, while those made of P. clematis lipids are completely resistant to it. However, if small amounts of SM are added to the P. clematis lipids, the resulting liposomes become sensitive to CL. Taken together, our results show for the first time that substitution of SM by its phosphono analogue is the molecular basis for the selectivity of an anthozoan toxin. We therefore propose that exotoxin production and membrane composition are coadapted traits that confer on the coelenterates a significant evolutionary advantage.


Assuntos
Proteínas Hemolisinas/toxicidade , Anêmonas-do-Mar , Esfingomielinas/farmacologia , Animais , Bovinos , Venenos de Cnidários , Eritrócitos/efeitos dos fármacos , Eritrócitos/fisiologia , Proteínas Hemolisinas/isolamento & purificação , Proteínas Hemolisinas/farmacologia , Lipossomos , Lipídeos de Membrana/sangue , Anêmonas-do-Mar/fisiologia
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