Cellular prion protein (PrP(C)) and superoxide dismutase (SOD) in vascular cells under oxidative stress


Autoria(s): SOPRANA, Helen Zocche; SOUZA, Liliete Canes; DEBBAS, Victor; LAURINDO, Francisco Rafael Martins
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

The PrP(C) is expressed in several cell types but its physiological function is unknown. Some studies associate the PrP(C) with copper metabolism and the antioxidant activity of SOD. Our hypothesis was that changes in PrP(C) expression lead to abnormal copper regulation and induce SOD downregulation in the vascular wall. Objectives: to study whether the PrP(C) expression undergoes induction by agents that trigger endoplasmic reticulum stress (ERS) and, in this context, to evaluate the SOD activity. Methods: To trigger ERS, in vitro, rabbit aortic smooth muscle cells were challenged for 4, 8 and 18 hours, with angiotensin-II, tunicamycin and 7-ketocholesterol. For in vivo studies rabbit aortic arteries were subjected to injury by balloon catheter. Results: In vitro baseline SOD activity, determined through inhibition of cytochrome-c reduction, was 13.9 +/- 1.2 U/mg protein, angiotensin-II exposed for 8 hours produced an increase in SOD activity, and cellular copper concentration was about 9 times greater only under these conditions. Western blotting analysis for SOD isoenzymes showed an expression profile that was not correlated with the enzymatic activity. PrP(C) expression decreased after exposure to all agents after different incubation periods. RT-PCR assay showed increased mRNA expression for PrP(C) only in cells stimulated for 8 hours with the different stressors. The PrP(C) mRNA expression in rabbit aortic artery fragments, subjected to balloon catheter injury, showed a pronounced increase immediately after overdistension. The results obtained indicated a PrP(C) protection factor during the early part of the ERS exposure period, but did not demonstrate a SOD-like profile for the PrP(C). (C) 2009 Elsevier GmbH. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) of Brazil

Identificador

EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, v.63, n.3, p.229-236, 2011

0940-2993

http://producao.usp.br/handle/BDPI/23677

10.1016/j.etp.2009.12.004

http://dx.doi.org/10.1016/j.etp.2009.12.004

Idioma(s)

eng

Publicador

ELSEVIER GMBH, URBAN & FISCHER VERLAG

Relação

Experimental and Toxicologic Pathology

Direitos

restrictedAccess

Copyright ELSEVIER GMBH, URBAN & FISCHER VERLAG

Palavras-Chave #Superoxide dismutase #Cellular prion protein #Rabbit aortic smooth muscle cells #Copper concentration #Endoplasmic reticulum stress #SMOOTH-MUSCLE-CELLS #ANGIOTENSIN-II #CARDIOVASCULAR-DISEASE #SIGNAL-TRANSDUCTION #OXIDANT STRESS #BALLOON INJURY #NADPH OXIDASE #BRAIN COPPER #IN-VIVO #EXPRESSION #Pathology #Toxicology
Tipo

article

original article

publishedVersion