Dopamine D2 receptor-mediated epidermal growth factor receptor transactivation through a disintegrin and metalloprotease regulates dopaminergic neuron development via extracellular signal-related kinase activation

Sehyoun Yoon, Ja-Hyun Baik

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Background:Dopamine D2R-mediated ERK activation regulates dopaminergic neuronal development. Results:D2R activation induces shedding of heparin-binding EGF by activating a disintegrin and metalloproteinase (ADAM) 10 or 17, causing EGFR transactivation in mesencephalic neurons. Conclusion:D2R-mediated ERK activation regulates mesencephalic dopaminergic neuron development via EGFR transactivation through ADAM10/17. Significance:Dopaminergic system alteration through D2R-ADAM-EGFR signaling maybe associated with dopamine-related neurological/psychiatric disorders.

Original languageEnglish
Pages (from-to)28435-28446
Number of pages12
JournalJournal of Biological Chemistry
Volume288
Issue number40
DOIs
Publication statusPublished - 2013 Oct 4

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Disintegrins
Dopamine D2 Receptors
Dopaminergic Neurons
Metalloproteases
Epidermal Growth Factor Receptor
Transcriptional Activation
Neurons
Dopamine
Phosphotransferases
Chemical activation
Nervous System Diseases
Epidermal Growth Factor
Psychiatry
Heparin

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

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title = "Dopamine D2 receptor-mediated epidermal growth factor receptor transactivation through a disintegrin and metalloprotease regulates dopaminergic neuron development via extracellular signal-related kinase activation",
abstract = "Background:Dopamine D2R-mediated ERK activation regulates dopaminergic neuronal development. Results:D2R activation induces shedding of heparin-binding EGF by activating a disintegrin and metalloproteinase (ADAM) 10 or 17, causing EGFR transactivation in mesencephalic neurons. Conclusion:D2R-mediated ERK activation regulates mesencephalic dopaminergic neuron development via EGFR transactivation through ADAM10/17. Significance:Dopaminergic system alteration through D2R-ADAM-EGFR signaling maybe associated with dopamine-related neurological/psychiatric disorders.",
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AU - Yoon, Sehyoun

AU - Baik, Ja-Hyun

PY - 2013/10/4

Y1 - 2013/10/4

N2 - Background:Dopamine D2R-mediated ERK activation regulates dopaminergic neuronal development. Results:D2R activation induces shedding of heparin-binding EGF by activating a disintegrin and metalloproteinase (ADAM) 10 or 17, causing EGFR transactivation in mesencephalic neurons. Conclusion:D2R-mediated ERK activation regulates mesencephalic dopaminergic neuron development via EGFR transactivation through ADAM10/17. Significance:Dopaminergic system alteration through D2R-ADAM-EGFR signaling maybe associated with dopamine-related neurological/psychiatric disorders.

AB - Background:Dopamine D2R-mediated ERK activation regulates dopaminergic neuronal development. Results:D2R activation induces shedding of heparin-binding EGF by activating a disintegrin and metalloproteinase (ADAM) 10 or 17, causing EGFR transactivation in mesencephalic neurons. Conclusion:D2R-mediated ERK activation regulates mesencephalic dopaminergic neuron development via EGFR transactivation through ADAM10/17. Significance:Dopaminergic system alteration through D2R-ADAM-EGFR signaling maybe associated with dopamine-related neurological/psychiatric disorders.

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