Base de dados : HANSEN
Pesquisa : MACROFAGOS/ENZIMOL [Descritor de assunto]
Referências encontradas : 3 [refinar]
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Id:18272
Autor:Yamashita, Kiyoaki; Iwamoto, Toshiyuki; Iijima, Soichi
Título:Immunohistochemical observation of lysozyme in macrophages in leprosy
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Fonte:s.l; s.n; sep. 1978. 7 p. ilus, tab.
Resumo:Lysozyme activities of skin granulomas of 24 patients in leprosy were studied. Lepra cells of all 15 lepromatous leprosy showed strong lysozyme activity in cytoplasma. In the specimens stained with lysozyme and Ziehl-Neelsen's carbolfuchsin double stain conspicuous lysozyme activity around M. leprae were observed. One borderline case was negative. Lysozyme of epithelioid cells and giant cells of 10 tuberculoid types were completely negative. These results suggest that lysozyme plays only a small role in the disposal of M. leprae in macrophages and other mechanisms than bacteriolytic function of lysozyme are responsible for the defence against these bacilli.(AU).
Descritores:HANSENIASE/enzimol
MACROFAGOS/enzimol
MACROFAGOS/microbiol
MURAMIDASE/metab
PELE/enzimol
MYCOBACTERIUM LEPRAE/citol
Limites:HUMANO
Meio Eletrônico: - .
Localização:BR191.1; 01308/s


  2 / 3 HANSEN  
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Id:18271
Autor:McKeever, Paul E; Walsh, Gerald P; Storrs, Eleanor E; Balentine, J. Douglas
Título:Electron microscopy of peroxidase and acid phosphatase in leprous and uninfected armadillo macrophages: a macrophage subpopulation contains peroxisomes and lacks bacilli
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Fonte:s.l; s.n; sep. 1978. 11 p. ilus.
Resumo:Lepromatous tissue from armadillos inoculated 24--36 months earlier with Mycobacterium leprae was obtained for electron microscopic studies. Cytochemically stained lepromas revealed a subpopulation of macrophages containing peroxisomes. These peroxidase reactive macrophages were not infected with bacilli. Acid phosphatase was present in macrophages and many of these were infected with bacilli and contained vacuoles and lipid globules. Within the membrane-bound vacuoles, acid phosphatase surrounded bacilli. However, the reaction product ended abruptly at a 15--40 millimicron thick zone of low electron density surrounding intact bacilli. Acid phosphatase was more intensely reactive and localized less precisely in heavily infected and vacuolated macrophages than in lightly and non-infected cells. The effectiveness of this bacillary barrier and the numerous infected macrophages with substantial acid phosphatase argue against the ability of acid phosphatase to protect host cells from leprosy bacilli. Evidence suggests a protective action of peroxidase or the rapid turnover of macrophages within lepromas. Granular and membranous debris were commonly seen within vacuoles of infected macrophages. A portion of the debris was ultrastructurally similar to bacillary matrix and was nonreactive for peroxidase and acid phosphatase. Following homogenization and centrifugation, similar materials banded with bacilli above 60% sucrose. Another portion of the debris was ultrastructurally similar to host lysosomal matrix and was reactive for acid phosphatase. Results support the concept of dual host and parasitic origins of the debris found in phagolysosomes of infected macrophages. Transparent, oval Epon defects remained eccentric to the majority of intact bacilli in centrifuged fractions. Apparently, an intrinsic property of leprosy produced these Epon defects.(AU).
Descritores:PEROXIDASES/metab
HISTOCITOQUIMICA
MODELOS ANIMAIS DE DOENCAS
MYCOBACTERIUM LEPRAE/isol
MACROFAGOS/enzimol
MACROFAGOS/microbiol
HANSENIASE/enzimol
HANSENIASE/microbiol
Limites:ESTUDO COMPARATIVO
ANIMAL
SUPPORT, U.S. GOV'T, P.H.S.
FOSFATASE ACIDA/*ME
TATUS
Meio Eletrônico: - .
Localização:BR191.1; 1307/s


  3 / 3 HANSEN  
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Id:18260
Autor:Shirahama, Tsuranobu; Cohen, Alan S
Título:Lysosomal breakdown of amyloid fibrils by macrophages
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Fonte:s.l; s.n; jun. 1971. 26 p. ilus, graf.
Resumo:Mouse peritoneal macrophages incubated with isolated human amyloid fibrils for varying periods of time up to 24 hours were studies by electron microscopy, and by electron microscopic cytochemistry for demonstration of acid phosphatase activity. The sequential changes in cytoplasmatic vacuoles in macrophages containing the amyloid fibrils and related material were analyzed and compared with those in controls and with direct enzymatic digestion of amyloid fibrils. the results suggest that the lysosome into amorphous, granular or finely filamentous material and absorbed, leaving undigested material as membranous or myeling the lysosomal enzymes into the amyloid-phagosome or the amyloid-phagolysosome was studied and interpreted as showing (1) fusion of primary lysosome (s) with the phagocytic vacuole, (2) autophagy of primary lysosome(s) into the heterophagic vacuole, and (3) transport of the enzymes into the phagocytic vacuole durectly from the Golgi associated vesicles or smooth endoplasmatic reticulum.(AU).
Descritores:APARELHO DE GOLGI/fisiol
FOSFATASE ACIDA/anal
AMILOIDE/metab
CITOPLASMA/fisiol
RETICULO ENDOPLASMATICO/fisiol
MACROFAGOS/enzimol
MACROFAGOS/patol
MACROFAGOS/fisiol
PERITÔNIO/citol
Limites:HUMANO
ANIMAL
CAMUNDONGOS
Meio Eletrônico: - .
Localização:BR191.1; 00056/s



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