Monocarboxylate 4 mediated butyrate transport in a rat intestinal epithelial cell line.

Dig Dis Sci

Section of Digestive Diseases, West Virginia Clinical and Translational Science Institute, West Virginia University Health Sciences Center, One Medical Center Drive, PO Box 9161, Morgantown, WV 26506, USA.

Published: March 2013

AI Article Synopsis

  • Short chain fatty acids (SCFA) are absorbed in the small intestine through specific transporters, with previous assumptions suggesting MCT1 as the main carrier for SCFA.
  • The study aimed to identify the transporter for butyrate in intestinal epithelial cells (IEC-18) by utilizing specific siRNAs to disrupt MCT1 and MCT4 functions.
  • Results showed that MCT1 is primarily responsible for lactate transport while MCT4 serves as the main transporter for butyrate, indicating distinct pathways for these substrates in intestinal absorption.

Article Abstract

Background: Short chain fatty acids (SCFA) are absorbed by carrier mediated uptake in the small intestine by pH-dependent SCFA/HCO3 (-) exchangers on the apical membrane of epithelial cells. Conventional assumption is that MCT1 mediates SCFA/HCO3 (-) exchange in the intestine. Further, due to the presence of multiple such anion exchangers, the identity of the intestinal SCFA/HCO3 (-) has been controversial.

Aims: The aim of this study was to determine the identities of the butyrate transporter in the intestinal epithelial cells (IEC-18).

Methods: IEC-18 cells were treated with specific siRNAs for MCT1 and MCT4, and butyrate and lactate uptake studies were performed.

Results: Alpha-cyano-4-hydroxycinnamic acid inhibited lactate uptake but not butyrate uptake in IEC-18 cells, indicating that these two substrates are transported via two different transporter systems. MCT1 siRNA treatment abolished both MCT1 mRNA by more than 95 % and protein expression by 83 % as evidenced by RTQ-PCR and western blotting experiments. However, MCT1 siRNA treatment inhibited butyrate uptake upto 24 %, whereas it inhibited lactate uptake significantly by 70 %. Treatment with MCT4 siRNA inhibited MCT4 mRNA expression by 75 % and protein expression by 85 % in these cells. MCT4 siRNA inhibited butyrate uptake by 40 %. Further, several non-steroidal anti-inflammatory drugs (NSAIDs) are transported by the butyrate transporter. Finally, MCT4 siRNA inhibited salicylate uptake by 27 % indicating direct evidence for the transport of salicylate by MCT4.

Conclusions: These data indicate that MCT1 is the high affinity lactate transporter and MCT4 is the high affinity butyrate transporter in the intestinal epithelial cell line IEC-18.

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http://dx.doi.org/10.1007/s10620-012-2407-xDOI Listing

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