ENT1 regulates ethanol-sensitive EAAT2 expression and function in astrocytes

Jinhua Wu, Moonnoh R. Lee, Sun Choi, Taehyun Kim, Doo Sup Choi

Research output: Contribution to journalArticle

38 Scopus citations

Abstract

Background: Equilibrative nucleoside transporter 1 (ENT1) and excitatory amino acid transporter 2 (EAAT2) are predominantly expressed in astrocytes where they are thought to regulate synaptic adenosine and glutamate levels. Because mice lacking ENT1 display increased glutamate levels in the ventral striatum, we investigated whether ENT1 regulates the expression and function of EAAT2 in astrocytes, which could contribute to altered glutamate levels in the striatum. Methods: We examined the effect of ENT1 inhibition and overexpression on the expression of EAAT2 using quantitative real-time PCR and measured glutamate uptake activity in cultured astrocytes. We also examined the effect of 0 to 200 mM ethanol doses for 0 to 24 hours of ethanol exposure on EAAT2 expression and glutamate uptake activity. We further examined the effect of ENT1 knockdown by a specific siRNA on ethanol-induced EAAT2 expression. Results: An ENT1-specific antagonist and siRNA treatments significantly reduced both EAAT2 expression and glutamate uptake activity while ENT1 overexpression up-regulated EAAT2 mRNA expression. Interestingly, 100 or 200 mM ethanol exposure increased EAAT2 mRNA expression as well as glutamate uptake activity. Moreover, we found that ENT1 knockdown inhibited the ethanol-induced EAAT2 up-regulation. Conclusions: Our results suggest that ENT1 regulates glutamate uptake activity by altering EAAT2 expression and function, which might be implicated in ethanol intoxication and preference.

Original languageEnglish (US)
Pages (from-to)1110-1117
Number of pages8
JournalAlcoholism: Clinical and Experimental Research
Volume34
Issue number6
DOIs
StatePublished - Jun 2010

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Keywords

  • Adenosine Uptake
  • Equilibrative Nucleoside Transporter 1 (ENT1)
  • Excitatory Amino Acid Transporter 2 (EAAT2)
  • Glutamate Uptake

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Toxicology
  • Psychiatry and Mental health

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