Abstract
Zinc release is a primary mediator of neuronal death. Here we show that zinc-mediated death of neurons in vitro is dependent on nerve growth factor (NGF) stimulation and does not occur in response to exposure to leukemia inhibitory factor. NGF priming is regulated, not by the traditional neurotrophin death receptor, p75NTR, but by TrkA, in a protein- and mRNA synthesis-dependent manner. Furthermore, Trk signaling promotes raised free intracellular zinc, mediating neuronal death after extracellular application of zinc. Thus, regulators of Trk signaling provide attractive targets for future treatment of zinc-associated neurological diseases, including stroke, epilepsy and brain trauma.
Publication types
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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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Cell Death / physiology*
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Cell Survival / drug effects
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Cells, Cultured
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Chelating Agents / pharmacology
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Colforsin / pharmacology
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Egtazic Acid / analogs & derivatives
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Egtazic Acid / pharmacology
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Enzyme Inhibitors / pharmacology
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Ganglia, Spinal / physiology
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Leukemia Inhibitory Factor / biosynthesis
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Leukemia Inhibitory Factor / physiology
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Mice
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Mice, Inbred C57BL
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Microscopy, Fluorescence
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Neurons / physiology*
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Proadifen / pharmacology
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Receptor, Nerve Growth Factor / biosynthesis
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Receptor, Nerve Growth Factor / physiology
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Receptor, trkA / antagonists & inhibitors
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Receptor, trkA / physiology*
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Receptors, Nerve Growth Factor / physiology
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Signal Transduction / physiology
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Zinc / metabolism
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Zinc / toxicity*
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Zinc Radioisotopes
Substances
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Chelating Agents
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Enzyme Inhibitors
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Leukemia Inhibitory Factor
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Receptor, Nerve Growth Factor
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Receptors, Nerve Growth Factor
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Zinc Radioisotopes
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Colforsin
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Egtazic Acid
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Proadifen
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Receptor, trkA
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Zinc
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1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid