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1.
Cell Death Dis ; 2: e209, 2011 Sep 08.
Artigo em Inglês | MEDLINE | ID: mdl-21900960

RESUMO

Granzyme B (GZMB) is a proapoptotic serine protease that is released by cytotoxic lymphocytes. However, GZMB can also be produced by other cell types and is capable of cleaving extracellular matrix (ECM) proteins. GZMB contributes to abdominal aortic aneurysm (AAA) through an extracellular, perforin-independent mechanism involving ECM cleavage. The murine serine protease inhibitor, Serpina3n (SA3N), is an extracellular inhibitor of GZMB. In the present study, administration of SA3N was assessed using a mouse Angiotensin II-induced AAA model. Mice were injected with SA3N (0-120 µg/kg) before pump implantation. A significant dose-dependent reduction in the frequency of aortic rupture and death was observed in mice that received SA3N treatment compared with controls. Reduced degradation of the proteoglycan decorin was observed while collagen density was increased in the aortas of mice receiving SA3N treatment compared with controls. In vitro studies confirmed that decorin, which regulates collagen spacing and fibrillogenesis, is cleaved by GZMB and that its cleavage can be prevented by SA3N. In conclusion, SA3N inhibits GZMB-mediated decorin degradation leading to enhanced collagen remodelling and reinforcement of the adventitia, thereby reducing the overall rate of rupture and death in a mouse model of AAA.


Assuntos
Proteínas de Fase Aguda/metabolismo , Aneurisma da Aorta Abdominal/patologia , Ruptura Aórtica/patologia , Decorina/metabolismo , Granzimas/metabolismo , Serpinas/metabolismo , Proteínas de Fase Aguda/genética , Proteínas de Fase Aguda/farmacologia , Angiotensina II/toxicidade , Animais , Aneurisma da Aorta Abdominal/metabolismo , Ruptura Aórtica/metabolismo , Apolipoproteínas E/genética , Apolipoproteínas E/metabolismo , Colágeno/metabolismo , Modelos Animais de Doenças , Granzimas/antagonistas & inibidores , Granzimas/genética , Camundongos , Camundongos Knockout , Processamento de Proteína Pós-Traducional/efeitos dos fármacos , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Proteínas Recombinantes/farmacologia , Serpinas/genética , Serpinas/farmacologia
2.
Am J Physiol Renal Physiol ; 296(4): F700-8, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19144689

RESUMO

Diabetic nephropathy, the leading cause of end-stage renal disease, is characterized by a proapoptotic and prooxidative environment. The mechanisms by which lifestyle interventions, such as exercise, benefit diabetic nephropathy are unknown. We hypothesized that exercise inhibits early diabetic nephropathy via attenuation of the mitochondrial apoptotic pathway and oxidative damage. Type 2 diabetic db/db and normoglycemic wild-type mice were exercised for an hour everyday at a moderate intensity for 7 wk, following which renal function, morphology, apoptotic signaling, and oxidative stress were evaluated. Exercise reduced body weight, albuminuria, and pathological glomerular expansion in db/db mice independent of hyperglycemic status. Changes in renal morphology were also related to reduced caspase-3 (main effector caspase in renal apoptosis), caspase-8 (main initiator caspase of the "extrinsic" pathway) activities, and TNF-alpha expression. A role for the mitochondrial apoptotic pathway was unlikely as both caspase-9 activity (initiator caspase of this pathway) and expression of regulatory proteins such as Bax and Bcl-2 were unchanged. Kidneys from db/db mice also produced higher levels of superoxides and had greater oxidative damage concurrent with downregulation of superoxide dismutase (SOD) 1 and 3. Interestingly, although exercise also increased superoxides, there was also upregulation of multiple SODs that likely inhibited lipid (hydroperoxides) and protein (carbonyls and nitrotyrosine) oxidation in db/db kidneys. In conclusion, exercise can inhibit progression of early diabetic nephropathy independent of hyperglycemia. Reductions in caspase-3 and caspase-8 activities, with parallel improvements in SOD expression and reduced oxidative damage, could underlie the beneficial effects of exercise in diabetic kidney disease.


Assuntos
Albuminúria/prevenção & controle , Apoptose , Caspase 3/metabolismo , Diabetes Mellitus Tipo 2/terapia , Nefropatias Diabéticas/prevenção & controle , Terapia por Exercício , Rim/enzimologia , Estresse Oxidativo , Fatores Etários , Albuminúria/enzimologia , Albuminúria/etiologia , Albuminúria/patologia , Animais , Caspase 8/metabolismo , Diabetes Mellitus Tipo 2/complicações , Diabetes Mellitus Tipo 2/enzimologia , Diabetes Mellitus Tipo 2/patologia , Nefropatias Diabéticas/enzimologia , Nefropatias Diabéticas/etiologia , Nefropatias Diabéticas/patologia , Modelos Animais de Doenças , Progressão da Doença , Regulação para Baixo , Rim/patologia , Masculino , Camundongos , Mitocôndrias/enzimologia , Mitocôndrias/patologia , Proteínas Proto-Oncogênicas c-bcl-2/metabolismo , Superóxido Dismutase/metabolismo , Fator de Necrose Tumoral alfa/metabolismo , Proteína X Associada a bcl-2/metabolismo
3.
Mycopathologia ; 155(4): 203-6, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12650596

RESUMO

A total of 576 dermatophytes were isolated from patients with a variety of skin infections from January 1993 to May 2000. Ten species of dermatophytes were identified: Epidermophyton floccosum (0.7%), Microsporum audouinii (1.1%), M. canis (3.1%), M. gypseum (0.3%), Trichophyton concentricum (3.5%), T. equinum (0.2%), T. mentagrophytes (36.1%), T. rubrum (53.8%), T. verrucosum (0.2) and T. violaceum (1.0%). The body sites most frequently affected by dermatophytes were the buttocks, nails and trunk. Anthropophilic dermatophytes made up 60.1% of the isolates; the most common species was T. rubrum, T. mentagrophytes and M. canis were the two main zoophilic dermatophytes. T. mentagrophytes was isolated from all body sites except the scalp. M. canis was found to be associated with domestic dogs and was not isolated from ethnic Malays. The only geophilic dermatophyte was M. gypseum, an uncommon dermatophyte associated with tinea pedis.


Assuntos
Arthrodermataceae/isolamento & purificação , Dermatomicoses/microbiologia , Arthrodermataceae/classificação , Dermatomicoses/epidemiologia , Humanos , Malásia/epidemiologia , Prevalência
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