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Glyceraldehyde-3-phosphate dehydrogenase, apoptosis, and neurodegenerative diseases.
Chuang, De-Maw; Hough, Christopher; Senatorov, Vladimir V.
Afiliación
  • Chuang DM; Molecular Neurobiology Section, Mood and Anxiety Disorders Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892-1363, USA. chuang@mail.nih.gov
Annu Rev Pharmacol Toxicol ; 45: 269-90, 2005.
Article en En | MEDLINE | ID: mdl-15822178
ABSTRACT
Increasing evidence supports the notion that glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a protein with multiple functions, including its surprising role in apoptosis. GAPDH is overexpressed and accumulates in the nucleus during apoptosis induced by a variety of insults in diverse cell types. Knockdown of GAPDH using an antisense strategy demonstrates its involvement in the apoptotic cascade in which GAPDH nuclear translocation appears essential. Knowledge concerning the mechanisms underlying GAPDH nuclear translocation and subsequent cell death is growing. Additional evidence suggests that GAPDH may be an intracellular sensor of oxidative stress during early apoptosis. Abnormal expression, nuclear accumulation, changes in physical properties, and loss of glycolytic activity of GAPDH have been found in cellular and transgenic models as well as postmortem tissues of several neurodegenerative diseases. The interaction of GAPDH with disease-related proteins as well as drugs used to treat these diseases suggests that it is a potential molecular target for drug development.
Asunto(s)
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Bases de datos: MEDLINE Asunto principal: Apoptosis / Enfermedades Neurodegenerativas / Gliceraldehído-3-Fosfato Deshidrogenasa (Fosforilante) Límite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos
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Bases de datos: MEDLINE Asunto principal: Apoptosis / Enfermedades Neurodegenerativas / Gliceraldehído-3-Fosfato Deshidrogenasa (Fosforilante) Límite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos