Abstract
Bcl-2-associated death protein (Bad), a member of the Bcl family, directs astrocytes in primary cultures to enter or resist apoptosis during ischemia in vitro. Under ischemia, Bad was the only Bcl family member whose expression was upregulated significantly during the early stages of an ischemic insult. Increased endogenous Bad was translocated from the cytoplasm to mitochondria to induce apoptosis in astrocytes. Concurrently, ischemia also induced Bad phosphorylation specifically on Ser112 to promote survival. This site-specific phosphorylation of Bad was mediated by an early activation of the mitogen-activated protein kinase/extracellular signal-regulated protein kinase (MAPK/ERK) intracellular signaling pathway. This study demonstrates that ischemia-induced Bad plays a dual role in determining whether astrocytes enter or resist apoptosis after an ischemic insult.
Copyright 2005 Wiley-Liss, Inc.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Apoptosis / drug effects
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Apoptosis / physiology*
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Astrocytes / physiology*
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Blotting, Western / methods
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Carrier Proteins / metabolism*
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Cells, Cultured
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Cerebral Cortex / cytology*
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Cytochromes c / metabolism
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Enzyme Induction / physiology
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Fluorescent Dyes / metabolism
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Gene Expression Regulation / physiology
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Green Fluorescent Proteins / genetics
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Green Fluorescent Proteins / metabolism
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Immunohistochemistry / methods
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Immunoprecipitation / methods
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In Situ Nick-End Labeling / methods
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Ischemia / metabolism*
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Mice
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Mice, Inbred ICR
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Mitochondria / metabolism
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Mitogen-Activated Protein Kinase Kinases / metabolism
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Models, Biological
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Mutagenesis, Site-Directed / physiology*
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Neurons / drug effects
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Phosphatidylinositol 3-Kinases / metabolism
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Phosphorylation
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Time Factors
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Transfection / methods
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bcl-Associated Death Protein
Substances
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Bad protein, mouse
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Carrier Proteins
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Fluorescent Dyes
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bcl-Associated Death Protein
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Green Fluorescent Proteins
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Cytochromes c
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Phosphatidylinositol 3-Kinases
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Mitogen-Activated Protein Kinase Kinases