Abundance and subcellular distribution of MCT1 and MCT4 in heart and fast-twitch skeletal muscles

被引:82
作者
Bonen, A [1 ]
Miskovic, D
Tonouchi, M
Lemieux, K
Wilson, MC
Marette, A
Halestrap, AP
机构
[1] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
[2] Univ Laval, Hosp Res Ctr, Lipid Res Unit, Dept Physiol, Quebec City, PQ G1V 4G2, Canada
[3] Univ Bristol, Dept Biochem, Bristol BS8 1TD, Avon, England
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2000年 / 278卷 / 06期
关键词
lactate; transport; transporters; fast-twitch fibers; plasma membrane; T tubules; messenger ribonucleic acid; monocarboxylate transporter 1; monocarboxylate transporter 4;
D O I
10.1152/ajpendo.2000.278.6.E1067
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The expression of two monocarboxylate transporters (MCTs) was examined in muscle and heart. MCT1 and MCT4 proteins are coexpressed in rat skeletal muscles, but only MCT1 is expressed in rat hearts. Among six rat fast-twitch muscles (red and white gastrocnemius, plantaris, extensor digitorum longus, red and white tibialis anterior) there was an inverse relationship between MCT1 and MCT4 (r = -0.94). MCT1 protein was correlated with MCT1 mRNA (r = 0.94). There was no relationship between MCT4 mRNA and MCT4 protein. MCT1 (r = -0.97) and MCT4 (r = 0.88) protein contents were correlated with percent fast-twitch glycolytic fiber. When normalized for their mRNAs, MCT1 but not MCT4 was still correlated with the percent fast-twitch glycolytic fiber composition of rat muscles (r = -0.98). MCT1 and MCT4 were also measured in plasma membranes (PM), triads (TR), T tubules (TT), sarcoplasmic reticulum (SR), and intracellular membranes (IM). There was an intracellular pool of MCT4 but not of MCT1. The MCT1 subcellular distribution was as follows: PM (100%) > TR (31.6%) > SR (15%) = TT (14%) > IM (1.7%). The MCT4 subcellular distribution was considerably different [PM (100%) > TR (66.5%) > (36%) = SR (43%) > IM (24%)]. These studies have shown that 1) the mechanisms regulating the expression of MCT1 (transcriptional and posttranscriptional) and MCT4 (posttranscriptional) are different and 2) differences in MCT1 and MCT4 expression among muscles, as well as in their subcellular locations, suggest that they may have different roles in muscle.
引用
收藏
页码:E1067 / E1077
页数:11
相关论文
共 39 条
[1]
Aivazachvili VA, 1998, FASEB J, V12, pA1032
[2]
ARMSTRONG RB, 1984, AM J ANAT, V171, P259, DOI 10.1002/aja.1001710303
[3]
Training intensity-dependent and tissue-specific increases in lactate uptake and MCT-1 in heart and muscle [J].
Baker, SK ;
McCullagh, KJA ;
Bonen, A .
JOURNAL OF APPLIED PHYSIOLOGY, 1998, 84 (03) :987-994
[4]
Palmitate transport and fatty acid transporters in red and white muscles [J].
Bonen, A ;
Luiken, JJFP ;
Liu, S ;
Dyck, DJ ;
Kiens, B ;
Kristiansen, S ;
Turcotte, LP ;
Van der Vusse, GJ ;
Glatz, JFC .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1998, 275 (03) :E471-E478
[5]
BONEN A, 1998, AM J PHYSIOL-ENDOC M, pE102
[6]
BONEN A, IN PRESS MED SCI SPO
[7]
Characterization of the monocarboxylate transporter 1 expressed in Xenopus laevis oocytes by changes in cytosolic pH [J].
Bröer, S ;
Schneider, HP ;
Bröer, A ;
Rahman, B ;
Hamprecht, B ;
Deitmer, JW .
BIOCHEMICAL JOURNAL, 1998, 333 :167-174
[8]
ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[9]
A new procedure for the isolation of plasma membranes, T tubules, and internal membranes from skeletal muscle [J].
Dombrowski, L ;
Roy, D ;
Marcotte, B ;
Marette, A .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1996, 270 (04) :E667-E676
[10]
ARIA, A PROTEIN THAT STIMULATES ACETYLCHOLINE-RECEPTOR SYNTHESIS, IS A MEMBER OF THE NEU LIGAND FAMILY [J].
FALLS, DL ;
ROSEN, KM ;
CORFAS, G ;
LANE, WS ;
FISCHBACH, GD .
CELL, 1993, 72 (05) :801-815