Molecular cloning, functional characterization and tissue distribution of rat H+/organic cation antiporter MATE1

Tomohiro Terada, Satohiro Masuda, Jun Ichi Asaka, Masahiro Tsuda, Toshiya Katsura, Ken Ichi Inui

Research output: Contribution to journalArticlepeer-review

110 Citations (Scopus)


Purpose. Transport characteristics and tissue distribution of the rat H+/organic cation antiporter MATE1 (multidrug and toxin extrusion 1) were examined. Methods. Rat MATE1 cDNA was isolated by polymerase chain reaction (PCR) cloning. Transport characteristics of rat MATE1 were assessed by HEK293 cells transiently expressing rat MATE1. The mRNA expression of rat MATE1 was examined by Northern blot and real-time PCR analyses. Results. The uptake of a prototypical organic cation tetraethylammonium (TEA) by MATE1-expressing cells was concentration-dependent, and showed the greatest value at pH 8.4 and the lowest at pH 6.0-6.5. Intracellular acidification induced by ammonium chloride resulted in a marked stimulation of TEA uptake. MATE1 transported not only organic cations such as cimetidine and metformin but also the zwitterionic compound cephalexin. MATE1 mRNA was expressed abundantly in the kidney and placenta, slightly in the spleen, but not expressed in the liver. Real-time PCR analysis of microdissected nephron segments showed that MATE1 was primarily expressed in the proximal convoluted and straight tubules. Conclusions. These findings indicate that MATE1 is expressed in the renal proximal tubules and can mediate the transport of various organic cations and cephalexin using an oppositely directed H+ gradient.

Original languageEnglish
Pages (from-to)1696-1701
Number of pages6
JournalPharmaceutical Research
Issue number8
Publication statusPublished - Aug 2006
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Molecular Medicine
  • Pharmacology
  • Pharmaceutical Science
  • Organic Chemistry
  • Pharmacology (medical)


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