articleJournal of Biological ChemistryApr 19, 2006HYBRID OA

Functional Repression of cAMP Response Element in 6-Hydroxydopamine-treated Neuronal Cells

EMElisabeth M. ChalovichJZJian-hui ZhuJCJohn CaltagaroneRBRobert BowserCTCharleen T. Chu

Inserm · University of Pittsburgh · +1 more institution

PubMed
Indexed incrossrefdoajpubmed

Abstract

Impaired survival signaling may represent a central mechanism in neurodegeneration. 6-Hydroxydopamine (6-OHDA) is an oxidative neurotoxin used to injure catecholaminergic cells of the central and peripheral nervous systems. Although 6-OHDA elicits phosphorylation of several kinases, downstream transcriptional effects that influence neuronal cell death are less defined. The cAMP response element (CRE) is present in the promoter sequences of several important neuronal survival factors. Treatment of catecholaminergic neuronal cell lines (B65 and SH-SY5Y) with 6-OHDA resulted in repression of basal CRE transactivation. Message levels of CRE-driven genes such as brain-derived neurotrophic factor and the survival…

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Authors

5
  • EM
    Elisabeth M. Chalovich

    Inserm, University of Pittsburgh, Collège de France

  • JZ
    Jian-hui Zhu

    University of Pittsburgh

  • JC
    John Caltagarone

    University of Pittsburgh

  • RB
    Robert Bowser

    University of Pittsburgh

  • CT
    Charleen T. ChuCorresponding

    University of Pittsburgh

Topics & keywords

Keywords
  • Neuroprotection
  • Receptor
  • Protein subunit
  • Chemistry
  • Pharmacology
  • Parkinson's disease
  • Kinase
  • Dopamine
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