Abstract
Expression of a cloned dopamine transporter complementary DNA in COS cells allows these primate kidney cells to accumulate the parkinsonism-inducing neurotoxin metabolite MPP+ (1-methyl-4-phenylpyridinium) avidly, and MPP+ toxicity results. By documenting that the dopamine transporter can confer MPP+ sensitivity to nonneural cells, these results highlight the key role that this transporter could play in mechanisms underlying parkinsonism.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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1-Methyl-4-phenylpyridinium / pharmacokinetics*
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1-Methyl-4-phenylpyridinium / poisoning
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Animals
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Carrier Proteins / genetics*
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Cell Line
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DNA / metabolism*
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Dopamine Plasma Membrane Transport Proteins
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Kidney / cytology
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Kidney / metabolism*
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Membrane Glycoproteins*
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Membrane Transport Proteins*
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Nerve Tissue Proteins / genetics
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Neurotoxins / pharmacokinetics
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Neurotoxins / poisoning
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Parkinson Disease, Secondary / chemically induced*
Substances
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Carrier Proteins
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Dopamine Plasma Membrane Transport Proteins
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Membrane Glycoproteins
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Membrane Transport Proteins
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Nerve Tissue Proteins
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Neurotoxins
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DNA
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1-Methyl-4-phenylpyridinium