Rosenberg S O, Fadil T, Schuster V L
Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461.
Biochem J. 1993 Jan 1;289 ( Pt 1)(Pt 1):263-8. doi: 10.1042/bj2890263.
Monolayers of Madin-Darby Canine Kidney (MDCK) cells grown on permeable filters generated lactate aerobically and accumulated it preferentially in the basolateral compartment, suggesting the presence of a lactate carrier. The mechanism of lactate transport across apical and basolateral membranes was examined by determining intracellular pH (pHi) microspectrofluorimetrically after addition of lactate to the extracellular solutions and by measuring uptake of [14C]lactate. Addition of 20 mM lactate to the apical compartment produced no change in pHi, whereas lactate added to the basolateral compartment rapidly and reversibly lowered pHi. Pyruvate produced similar results. Inhibitors of lactate/H+ co-transporters, alpha-cyano-4-hydroxycinnamate (CnCN) and quercetin, partially inhibited the fall in pHi produced by basolateral lactate. In contrast, the disulphonic stilbene. DIDS (4,4'-di-isothiocyanostilbene-2,2'-disulphonic acid) produced no inhibition at 0.5 mM. Kinetic analysis was performed by applying basolateral lactate at various concentrations and measuring the rate of entry (delta pHi/min) in the presence and absence of CnCN. Lactate flux was shown to occur by both non-ionic diffusion and a alpha-cyano-4-hydroxycinnamate-sensitive component (carrier). The latter has a Km of approximately 7 mM for the lactate anion. Propionate, but not formate, lowered pHi to the same degree as did equimolar lactate, but the propionate effect was not inhibited by CnCN. Influx of [14C]lactate was substantially greater across the basolateral membrane than across the apical membrane and occurred in the absence of Na+. We conclude that MDCK cells grown on permeable filters generate lactate aerobically and transport it across the basolateral membrane by way of a lactate/H+ cotransporter.
在可渗透滤膜上生长的麦迪逊-达比犬肾(MDCK)细胞单层在有氧条件下产生乳酸,并优先在基底外侧隔室中积累,这表明存在乳酸载体。通过在细胞外溶液中添加乳酸后用显微分光荧光法测定细胞内pH(pHi)以及测量[14C]乳酸的摄取,研究了乳酸跨顶膜和基底外侧膜的转运机制。向顶室添加20 mM乳酸不会使pHi发生变化,而添加到基底外侧隔室的乳酸会迅速且可逆地降低pHi。丙酮酸产生了类似的结果。乳酸/氢离子共转运体抑制剂α-氰基-4-羟基肉桂酸(CnCN)和槲皮素部分抑制了基底外侧乳酸引起的pHi下降。相比之下,二磺酸芪(DIDS,4,4'-二异硫氰酸芪-2,2'-二磺酸)在0.5 mM时没有产生抑制作用。通过施加不同浓度的基底外侧乳酸并在存在和不存在CnCN的情况下测量进入速率(ΔpHi/分钟)进行动力学分析。结果表明,乳酸通量通过非离子扩散和α-氰基-4-羟基肉桂酸敏感成分(载体)发生。后者对乳酸阴离子的Km约为7 mM。丙酸盐而非甲酸盐使pHi降低的程度与等摩尔乳酸相同,但丙酸盐的作用不受CnCN抑制。[14C]乳酸跨基底外侧膜的流入量比跨顶膜的流入量要大得多,并且在没有钠离子的情况下也会发生。我们得出结论,在可渗透滤膜上生长的MDCK细胞在有氧条件下产生乳酸,并通过乳酸/氢离子共转运体将其转运穿过基底外侧膜。