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Int J Lepr Other Mycobact Dis ; 66(3): 365-73, 1998 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9934363

RESUMO

We measured the release of reactive oxygen intermediaries [ROI (hydrogen peroxide and superoxide anion)] by murine peritoneal macrophages challenged in vitro with Mycobacterium lepraemurium (MLM), complement-opsonized yeast, M. bovis BCG, M. phlei, or phorbol myristate acetate (PMA). We found that except for MLM, all of the other materials provoked the release of significant amounts of hydrogen peroxide and superoxide. MLM entered the macrophages without triggering their oxidative metabolism. Pre-infection of macrophages with MLM did not alter these cells' capacity to release the normal amounts of ROI in response to other microorganisms or PMA. Killing of MLM did not revert the macrophages' failure to release ROI upon ingestion of the microorganism, nor were macrophages able to produce these toxic metabolites when pre-incubated in the presence of murine gamma interferon (IFN-gamma). MLM has several attributes that allow it to survive within macrophages: a) it is a nontoxigenic microorganism (it does not harm its host), b) it resists the harsh conditions of the intraphagolysosomal milieu (a property perhaps dependent on its thick lipidic envelope), and c) it penetrates the macrophages without triggering their oxidative response (thus avoiding the generation of the toxic intermediaries of oxygen). For these attributes (and others discussed in this paper), we recognize MLM as a highly evolved, well-adapted parasite of macrophages. In addition, the results of the present study prompted the analysis of the biochemical pathways used by MLM and M. bovis BCG to penetrate into their cellular hosts, a subject now under investigation in our laboratory.


Assuntos
Macrófagos Peritoneais/microbiologia , Mycobacterium lepraemurium/fisiologia , Espécies Reativas de Oxigênio/metabolismo , Animais , Células Cultivadas , Feminino , Peróxido de Hidrogênio/metabolismo , Interferon gama/farmacologia , Macrófagos Peritoneais/efeitos dos fármacos , Macrófagos Peritoneais/metabolismo , Camundongos , Mycobacterium bovis/fisiologia , Mycobacterium phlei/fisiologia , Proteínas Recombinantes , Saccharomyces cerevisiae/fisiologia , Superóxidos/metabolismo , Acetato de Tetradecanoilforbol/farmacologia
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