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Early phase of amyloid beta42-induced cytotoxicity in neuronal cells is associated with vacuole formation and enhancement of exocytosis
Experimental & Molecular Medicine ; : 559-566, 2005.
Artigo em Inglês | WPRIM | ID: wpr-191495
ABSTRACT
Amyloid beta (Abeta) neurotoxicity is believed to play a critical role in the pathogenesis of Alzheimer's disease (AD) mainly because of its deposition in AD brain and its neuronal toxicity. However, there have been discrepancies in Abeta-induced cytotoxicity studies, depending on the assay methods. Comparative analysis of Abeta42-induced in vitro cytotoxicity might be useful to elucidate the etiological role of Abeta in the pathogenesis of AD. In this study, MTT, CCK-8, calcein-AM/EthD-1 assays as well as thorough microscopic examinations were comparatively performed after Abeta42 treatment in a neuronal precursor cells (NT2) and a somatic cells (EcR293). Extensive formation of vacuoles was observed at the very early stage of Abeta42 treatment in both cells. Early observation of Abeta42 toxicity as seen in vacuole formation was also shown in MTT assay, but not in CCK-8 and calcein-AM/EthD-1 assays. In addition, Abeta42 treatment dramatically accelerated MTT formazan exocytosis, implying its effect on the extensive formation of cytoplasmic vacuoles. Abeta42 seems to cause indirect inhibition on the intracellular MTT reduction as well as vacuole formation and exocytosis enhancement. Following the acute cellular dysfunction induced by Abeta42, the prolonged treatment of micromolar concentration of Abeta42 resulted in slight inhibition on redox and esterase activity. The early Abeta42-induced vacuolated morphology and later chronic cytotoxic effect in neuronal cell might be linked to the chronic neurodegeneration caused by the accumulation of Abeta42 in AD patients' brain.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fragmentos de Peptídeos / Sais de Tetrazólio / Fatores de Tempo / Vacúolos / Linhagem Celular / Peptídeos beta-Amiloides / Morte Celular / Relação Dose-Resposta a Droga / Exocitose / Formazans Limite: Animais Idioma: Inglês Revista: Experimental & Molecular Medicine Ano de publicação: 2005 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fragmentos de Peptídeos / Sais de Tetrazólio / Fatores de Tempo / Vacúolos / Linhagem Celular / Peptídeos beta-Amiloides / Morte Celular / Relação Dose-Resposta a Droga / Exocitose / Formazans Limite: Animais Idioma: Inglês Revista: Experimental & Molecular Medicine Ano de publicação: 2005 Tipo de documento: Artigo