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Non-selective cation channels and oxidative stress-induced cell swelling
Simon, Felipe; Varela, Diego; Riveros, Ana; Eguiguren, Ana Luisa; Stutzin, Andres.
  • Simon, Felipe; Universidad de Chile. Facultad de Medicina. Instituto de Ciencias Biomédicas. Programa de Fisiopatología. Laboratorio de Fisiopatología Molecular. CL
  • Varela, Diego; Universidad de Chile. Facultad de Medicina. Instituto de Ciencias Biomédicas. Programa de Fisiopatología. Laboratorio de Fisiopatología Molecular. CL
  • Riveros, Ana; Universidad de Chile. Facultad de Medicina. Instituto de Ciencias Biomédicas. Programa de Fisiopatología. Laboratorio de Fisiopatología Molecular. CL
  • Eguiguren, Ana Luisa; Universidad de Chile. Facultad de Medicina. Instituto de Ciencias Biomédicas. Programa de Fisiopatología. Laboratorio de Fisiopatología Molecular. CL
  • Stutzin, Andres; Universidad de Chile. Facultad de Medicina. Instituto de Ciencias Biomédicas. Programa de Fisiopatología. Laboratorio de Fisiopatología Molecular. CL
Biol. Res ; 35(2): 215-222, 2002. graf
Artigo em Inglês | LILACS | ID: lil-323344
RESUMO
Necrosis is considered as a non-specific form of cell death that induces tissue inflammation and is preceded by cell swelling. This increase in cell volume has been ascribed mainly to defective outward pumping of Na+ caused by metabolic depletion and/or to increased Na+ influx via membrane transporters. A specific mechanism of swelling and necrosis driven by the influx of Na+ through nonselective cation channels has been recently proposed (Barros et al., 2001a). We have characterized further the properties of the nonselective cation channel (NSCC) in HTC cells. The NSCC shows a conductance of approximately 18 pS, is equally permeable to Na+ and K+, impermeant to Ca2+, requires high intracellular Ca2+ as well as low intracellular ATP for activation and is inhibited by flufenamic acid. Hydrogen peroxide induced a significant increase in cell volume that was dependent on external Na+. We propose that the NSCC, which is ubiquitous though largely inactive in healthy cells, becomes activated under severe oxidative stress. The ensuing Na+ influx initiates via positive feedback a series of metabolic and electrolytic disturbances, resulting in cell death by necrosis
Assuntos
Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Carcinoma Hepatocelular / Estresse Oxidativo / Canais Iônicos / Neoplasias Hepáticas Limite: Animais Idioma: Inglês Revista: Biol. Res Assunto da revista: Biologia Ano de publicação: 2002 Tipo de documento: Artigo / Documento de projeto País de afiliação: Chile Instituição/País de afiliação: Universidad de Chile/CL

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Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Carcinoma Hepatocelular / Estresse Oxidativo / Canais Iônicos / Neoplasias Hepáticas Limite: Animais Idioma: Inglês Revista: Biol. Res Assunto da revista: Biologia Ano de publicação: 2002 Tipo de documento: Artigo / Documento de projeto País de afiliação: Chile Instituição/País de afiliação: Universidad de Chile/CL