Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle
Article first published online: 12 AUG 2004
The Journal of Physiology
Volume 529, Issue 2, pages 285–293, December 2000
How to Cite
Fox, J. E. M., Meredith, D. and Halestrap, A. P. (2000), Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle. The Journal of Physiology, 529: 285–293. doi: 10.1111/j.1469-7793.2000.00285.x
- Issue published online: 12 AUG 2004
- Article first published online: 12 AUG 2004
- (Received 8 May 2000; accepted after revision 3 August 2000)
- 1Monocarboxylate transporter (MCT) 4 is the major monocarboxylate transporter isoform present in white skeletal muscle and is responsible for the efflux of lactic acid produced by glycolysis. Here we report the characterisation of MCT4 expressed in Xenopus oocytes.
- 2The protein was correctly targeted to the plasma membrane and rates of substrate transport were determined from the rate of intracellular acidification monitored with the pH-sensitive dye 2′,7′-bis-(carboxyethyl)-5(6)-carboxyfluorescein (BCECF).
- 3In order to validate the technique, the kinetics of monocarboxylate transport were measured in oocytes expressing MCT1. Km values determined for L-lactate, D-lactate and pyruvate of 4.4, > 60 and 2.1 mM, respectively, were similar to those determined previously in tumour cells.
- 4Comparison of the time course of [14C]lactate accumulation with the rate of intracellular acidification monitored with BCECF suggests that the latter reflects pH changes close to the plasma membrane associated with transport, whilst the former may include diffusion-limited movement of lactate into the bulk cytosol.
- 5Km values of MCT4 for these substrates were found to be 28, 519 and 153 mM, respectively, and for a range of other monocarboxylates values were at least an order of magnitude higher than for MCT1. Vmax values appeared to be similar for all substrates.
- 6K0.5 values of MCT4 (determined at 30 mM L-lactate) for inhibition by α-cyano-4-hydroxycinnamate (991 μM), phloretin (41 μM), 5-nitro-2-(3-phenylpropylamino)benzoate (240 μM), p-chloromercuribenzene sulphonate (21 μM) and 3-isobutyl-1-methylxanthine (970 μM, partial inhibition) were also substantially higher than for MCT1. No inhibition of MCT4 by 2 mM 4,4′-diisothiocyanostilbene-2,2′-disulphonate was observed.
- 7The properties of MCT4 are consistent with published data on giant sarcolemmal vesicles in which MCT4 is the dominant MCT isoform, and are appropriate for the proposed role of MCT4 in mediating the efflux from the cell of glycolytically derived lactic acid but not pyruvate.