Chen J, Zhu Y, Hu M
Department of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Pullman 99164-6510.
J Nutr. 1994 Oct;124(10):1907-16. doi: 10.1093/jn/124.10.1907.
Mechanism and kinetics of uptake and efflux of L-methionine in a human intestinal epithelial model system (Caco-2) were studied to understand the transcellular transport process and to determine its rate-limiting step. The kinetic studies indicated that uptakes from both the apical and basolateral sides were saturable [for apical uptake: Km = 0.96 mmol/L, maximum flux = 673 pmol/(min.cm2); for basolateral uptake: Km = 3.46 mmol/L, maximum flux = 3480 pmol/(min.cm2)], whereas the efflux from these two membranes was apparently linear for intracellular concentrations < 6.5 mmol/L [for apical efflux, the apparent first-order rate constant = 1.01 x 10(-4) cm/min; for basolateral efflux, the rate constant = 1.78 x 10(-4) cm/min]. The results of inhibition studies indicate the apical uptake is partially active and Na(+)-dependent via a combination of amino acid transport systems B0,+ and ASC, which is somewhat different from the less energy- and Na(+)-dependent basolateral uptake. The basolateral uptake is also more dependent on system L and exhibits high counter-exchange capability. Finally, the rate-limiting step in the apical to basolateral transport of methionine is determined to be the basolateral efflux.
为了解L-蛋氨酸在人肠上皮模型系统(Caco-2)中的摄取和外排机制及动力学,以明确其跨细胞转运过程并确定限速步骤。动力学研究表明,从顶端和基底外侧的摄取均具有饱和性[顶端摄取:Km = 0.96 mmol/L,最大通量 = 673 pmol/(min·cm2);基底外侧摄取:Km = 3.46 mmol/L,最大通量 = 3480 pmol/(min·cm2)],而当细胞内浓度 < 6.5 mmol/L时,从这两个膜的外排明显呈线性[顶端外排,表观一级速率常数 = 1.01×10(-4) cm/min;基底外侧外排,速率常数 = 1.78×10(-4) cm/min]。抑制研究结果表明,顶端摄取部分具有活性且通过氨基酸转运系统B0,+和ASC的组合依赖于Na(+),这与能量和Na(+)依赖性较低的基底外侧摄取有所不同。基底外侧摄取也更依赖于系统L并表现出高反向交换能力。最后,确定蛋氨酸从顶端到基底外侧转运的限速步骤为基底外侧外排。