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1.
BMC Res Notes ; 3: 151, 2010 May 27.
Artigo em Inglês | MEDLINE | ID: mdl-20507618

RESUMO

BACKGROUND: In the last years, plants are being used for the production of a wide variety of biopharmaceuticals, including cytokines, and have the potential to serve as vehicles for mucosal administration of these molecules. We had previously reported the expression of a cytokine, interleukin-12 (IL-12), in transgenic tomato plants and had demonstrated that it retained its biologic activity in vitro. FINDINGS: In this work, we administered crude extracts of IL-12-containing tomato fruits to mice through the intratracheal route, measuring endogenous IL-12 and determining biologic activity by quantification of interferon-gamma (IFN-gamma) in lungs and by histological analysis. IFN-gamma expression in lungs, as well as histological analysis, indicate that tomato-expressed IL-12 retains its biologic activity and, most importantly, its effects are restricted to the site of administration. CONCLUSION: Our results indicate that the functional activity of tomato-expressed IL-12 is comparable to that of commercial recombinant IL-12 when given via the mucosal route. This opens the possibility of using crude extracts prepared from tomatoes expressing IL-12 for certain immunotherapies.

2.
Cell Biol Int ; 33(9): 1026-31, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19524691

RESUMO

Treatment of P388D1, a macrophage-like cell line, with staurosporine triggered apoptosis through the activation of caspase-9 and caspase-3. Unexpected effects of staurosporine on the induction of apoptosis were the activation of caspase-8, and an increase of the levels of TNF-alpha. The increased TNF-alpha levels led to activation of caspase-8 by an autocrine effect via the TNF receptor expressed by the P388D1 macrophages. In contrast, P388D1 macrophages that either had been exposed to UV light or treated with dexamethasone did not undergo apoptosis.


Assuntos
Apoptose , Macrófagos/efeitos dos fármacos , Inibidores de Proteínas Quinases/farmacologia , Estaurosporina/farmacologia , Animais , Antineoplásicos Hormonais/farmacologia , Caspase 3/efeitos dos fármacos , Caspase 3/metabolismo , Caspase 8/efeitos dos fármacos , Caspase 8/metabolismo , Caspase 9/efeitos dos fármacos , Caspase 9/metabolismo , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Sobrevivência Celular/fisiologia , Fragmentação do DNA/efeitos dos fármacos , Dexametasona/farmacologia , Macrófagos/efeitos da radiação , Camundongos , Receptores Tipo I de Fatores de Necrose Tumoral/agonistas , Receptores Tipo I de Fatores de Necrose Tumoral/metabolismo , Transdução de Sinais/efeitos dos fármacos , Transdução de Sinais/fisiologia , Fator de Necrose Tumoral alfa/biossíntese , Fator de Necrose Tumoral alfa/efeitos dos fármacos , Raios Ultravioleta/efeitos adversos
3.
Virol J ; 5: 127, 2008 Oct 25.
Artigo em Inglês | MEDLINE | ID: mdl-18950517

RESUMO

Cell-surface viral proteins most frequently enter the cell through clathrin or caveolae endocytosis. Respiratory syncytial virus antigen internalization by immune cells is via caveolin, however, uptake of paramyxovirus cell membrane proteins by non-immune cells is done through clathrin-coated pits. In this work, the uptake of respiratory syncytial virus cell surface glycoproteins by non-immune human epithelial cells was investigated through indirect immunofluorescence with polyclonal anti-RSV antibody and confocal lasser-scanner microscopy. Clathrin and caveolae internalization pathways were monitored through specific inhibitors monodansylcadaverine (MDC) and methyl-beta-cyclodextrin (MBCD), respectively. Internalization of RSV antigens was inhibited by MDC but not by MBCD, implying that clathrin-mediated endocytosis is the major uptake route of RSV antigens by an epithelial human cell line.


Assuntos
Vesículas Revestidas por Clatrina/virologia , Endocitose , Células Epiteliais/virologia , Glicoproteínas/metabolismo , Vírus Sinciciais Respiratórios/fisiologia , Proteínas Virais/metabolismo , Cadaverina/análogos & derivados , Cadaverina/farmacologia , Linhagem Celular , Inibidores Enzimáticos/farmacologia , Técnica Indireta de Fluorescência para Anticorpo , Humanos , Microscopia Confocal , beta-Ciclodextrinas/farmacologia
4.
Virol J ; 4: 68, 2007 Jul 03.
Artigo em Inglês | MEDLINE | ID: mdl-17608950

RESUMO

BACKGROUND: The binding of viral-specific antibodies to cell-surface antigens usually results in down modulation of the antigen through redistribution of antigens into patches that subsequently may be internalized by endocytosis or may form caps that can be expelled to the extracellular space. Here, by use of confocal-laser-scanning microscopy we investigated the kinetics of the modulation of respiratory syncytial virus (RSV) antigen by RSV-specific IgG. RSV-infected human epithelial cells (HEp-2) were incubated with anti-RSV polyclonal IgG and, at various incubation times, the RSV-cell-surface-antigen-antibody complexes (RSV Ag-Abs) and intracellular viral proteins were detected by indirect immunoflourescence. RESULTS: Interaction of anti-RSV polyclonal IgG with RSV HEp-2 infected cells induced relocalization and aggregation of viral glycoproteins in the plasma membrane formed patches that subsequently produced caps or were internalized through clathrin-mediated endocytosis participation. Moreover, the concentration of cell surface RSV Ag-Abs and intracellular viral proteins showed a time dependent cyclic variation and that anti-RSV IgG protected HEp-2 cells from viral-induced death. CONCLUSION: The results from this study indicate that interaction between RSV cell surface proteins and specific viral antibodies alter the expression of viral antigens expressed on the cells surface and intracellular viral proteins; furthermore, interfere with viral induced destruction of the cell.


Assuntos
Anticorpos Antivirais/imunologia , Antígenos Virais/imunologia , Células Epiteliais/imunologia , Células Epiteliais/virologia , Vírus Sinciciais Respiratórios/imunologia , Animais , Linhagem Celular Tumoral , Clatrina/metabolismo , Endocitose/fisiologia , Células Epiteliais/citologia , Glicoproteínas/metabolismo , Humanos , Imunoglobulina G/imunologia , Imunoglobulina G/metabolismo , Cinética , Masculino , Coelhos , Proteínas Virais/metabolismo
5.
Prog. obstet. ginecol. (Ed. impr.) ; 49(10): 606-610, oct. 2006. ilus
Artigo em Es | IBECS | ID: ibc-048503

RESUMO

Aunque el dolor pélvico y la metrorragia son las alteraciones más frecuentemente asociadas al mioma uterino, el hemoperitoneo agudo por rotura de leiomioma subseroso es un hecho excepcional apenas recogido en la literatura médica internacional. Este artículo describe uno de los pocos casos conocidos de abdomen agudo por rotura espontánea de leiomioma uterino subseroso que hemos tenido ocasión de tratar en el Servicio de Ginecología del Hospital Universitario Central de Asturias. La edad de la paciente, la paridad, el tamaño del mioma y ciertas malformaciones vasculares uterinas son considerados factores de riesgo para este cuadro tan insólito, pero además, en nuestro caso, determinadas peculiaridades histológicas del tumor parecen tener cierta relevancia


Although pelvic pain and metrorrhagia are the disorders that are most commonly associated with uterine leiomyoma, acute hemoperitoneum due to rupture of a subserosal leiomyoma is an exceptional event that has scarcely been reported in the international medical literature. This article describes one of the few known cases of acute abdomen caused by spontaneous rupture of a subserosal uterine leiomyoma, which was treated at the Department of Gynecology of the Hospital Universitario Central de Asturias (Spain). Risk factors for this unusual entity are considered to be the patient's age and parity, as well as the size of the myoma and certain uterine vascular malformations; however, in this specific case, some histological peculiarities of the tumor seem to be of relevance


Assuntos
Feminino , Humanos , Leiomioma/complicações , Abdome Agudo/etiologia , Ruptura Espontânea/complicações , Hemoperitônio/etiologia
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