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The characterization of butyrate transport across pig and human colonic luminal membrane
Author(s) -
Ritzhaupt Armin,
Ellis Antony,
Hosie Ken B.,
ShiraziBeechey Soraya P.
Publication year - 1998
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.1998.819bs.x
Subject(s) - butyrate , dids , propionate , chemistry , mersalyl , biochemistry , cotransporter , ion transporter , bicarbonate , membrane , mitochondrion , sodium , organic chemistry , fermentation
1 Luminal membrane vesicles (LMV) were isolated from human and pig colonic tissues. They were characterized in terms of purity and ability to transport [ 14 C]butyrate. 2 The activity of cysteine‐sensitive alkaline phosphatase, and the abundance of villin, NHE2 and NHE3 proteins, markers of the colonic luminal membrane, were significantly enriched in the LMV compared with the original cellular homogenate. The LMV were free from contamination by other cellular organelles and basolateral membranes, as revealed by the negligible presence of either specific marker enzyme activity or characteristic immunogenic protein. 3 The transport of butyrate into the luminal membrane vesicles was enhanced 5‐fold at pH 5.5 compared with pH 8.0. Butyrate transport was temperature dependent, and was stimulated in the presence of an outward‐directed anion gradient in the order of butyrate > bicarbonate > propionate > chloride. Kinetic analysis of increasing substrate concentration showed saturation kinetics with an apparent K m value of 14.8 ± 3.6 mM and a V max of 54 ± 14 nmol min −1 (mg protein) −1 . 4 Butyrate transport was significantly reduced in the presence of short chain fatty acids (SCFA), acetate, propionate and other monocarboxylates (pyruvate and L‐lactate). Butyrate uptake was inhibited by several cysteine group modifying reagents such as p ‐chloromercuribenzosulphonic acid (pCMBS), p ‐chloromercuribenzoate (pCMB), mersalyl acid and HgCl 2 , but not by the stilbene anion exchange inhibitors, 4,4′‐diisothiocyanostilbene‐2,2′‐disulphonate (DIDS) and 4,4′‐dinitrostilbene‐2,2′‐disulphonate (SITS). 5 The described properties of butyrate transport across the luminal pole of the colon suggest the involvement of a carrier protein, in the form of a pH‐activated anion exchange process. The transporter is distinct from the erythrocyte band‐3 type anion exchanger and may belong to the monocarboxylate‐type transport proteins (MCT1).