Inactivation of monocarboxylate transporter MCT3 by DNA methylation in atherosclerosis

Shoukang Zhu, Pascal J. Goldschmidt-Clermont, Chunming Dong

Research output: Contribution to journalArticle

52 Scopus citations

Abstract

Background - Monocarboxylate transporters (MCTs) mediate lactate transport across the plasma membrane of cells. The molecular mechanisms regulating monocarboxylate transport in smooth muscle cells (SMCs) remain poorly characterized. The aim of this study was to investigate the effects of DNA methylation on MCT expression and lactate transport in SMCs in relation to atherosclerosis. Methods and Results - MCT expression was determined by real-time reverse transcription-polymerase chain reaction, Western blotting, and immunohistochemistry in SMCs isolated from human aortas and coronary arteries. Bisulfite sequencing and confocal microscopic analysis were used to study DNA methylation and lactate transport in SMCs, respectively. Downregulation of MCT3 and impaired lactate transport were detected in proliferating/synthetic SMCs, relative to the contractile phenotype. A passage number- and atherosclerotic lesion-dependent methylation pattern of MCT3 was demonstrated in the CpG island located in exon 2. Treatment of SMCs with the demethylating agent 5-aza-2′-deoxycytidine restored MCT3 expression and normalized lactate transport. Furthermore, small interfering RNA-mediated specific MCT3 knockdown substantially stimulated SMC proliferation. Conclusions - These data indicate that DNA methylation may modify monocarboxylate transport by suppressing MCT3 expression, which could be important in regulating SMC function and the development of atherosclerosis.

Original languageEnglish (US)
Pages (from-to)1353-1361
Number of pages9
JournalCirculation
Volume112
Issue number9
DOIs
StatePublished - Aug 30 2005

Keywords

  • Atherosclerosis
  • Cardiovascular diseases
  • Ion channels
  • Molecule biology
  • Muscle, smooth

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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