Mechanism(s) of butyrate transport in Caco-2 cells: role of monocarboxylate transporter 1

被引:148
作者
Hadjiagapiou, C
Schmidt, L
Dudeja, PK
Layden, TJ
Ramaswamy, K
机构
[1] Univ Illinois, Dept Med, Sect Digest & Liver Dis, Chicago, IL 60612 USA
[2] W Side Vet Adm Med Ctr, Chicago, IL 60612 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2000年 / 279卷 / 04期
关键词
short-chain fatty acids; intestinal absorption; antisense cDNA;
D O I
10.1152/ajpgi.2000.279.4.G775
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The short-chain fatty acid butyrate was readily taken up by Caco-2 cells. Transport exhibited saturation kinetics, was enhanced by low extracellular pH, and was Na+ independent. Butyrate uptake was unaffected by DIDS; however, alpha-cyano-4-hydroxycinnamate and the butyrate analogs propionate and L-lactate significantly inhibited uptake. These results suggest that butyrate transport by Caco-2 cells is mediated by a transporter belonging to the monocarboxylate transporter family. We identified five isoforms of this transporter, MCT1, MCT3, MCT4, MCT5, and MCT6, in Caco-2 cells by PCR, and MCT1 was found to be the most abundant isoform by RNase protection assay. Transient transfection of MCT1, in the antisense orientation, resulted in significant inhibition of butyrate uptake. The cells fully recovered from this inhibition by 5 days after transfection. In conclusion, our data showed that the MCT1 transporter may play a major role in the transport of butyrate into Caco-2 cells.
引用
收藏
页码:G775 / G780
页数:6
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