Jessen H, Røigaard H, Riahi-Esfahani S, Jacobsen C
Institute of Medical Biochemistry, University of Aarhus, Denmark.
Biochim Biophys Acta. 1994 Mar 23;1190(2):279-88. doi: 10.1016/0005-2736(94)90085-x.
We investigated whether an immortalized human kidney epithelial cell line (IHKE), compared with normal embryonic cells (NHKE), can be used as a representative system with which to characterize the transport of neutral amino acids in the proximal tubule of the human kidney. The IHKE cell line, immortalized by treatment with NiSO4, exhibited microvilli and enzyme markers specific for highly specialized tubule cells. The Na(+)-dependent uptake of alpha-aminoisobutyric acid (AIB) by IHKE and NHKE cells occurred by means of a single transport system with identical half-saturation constants, but the capacity for uptake was higher in the immortalized cells. Proton-dependent influx of AIB was also mediated by a single transport component with similar uptake characteristics in both types of cells. Imposition of an H(+)-gradient to a Na(+)-gradient reduced the sodium dependent uptake of AIB with the exception of short incubation time (1 min), where addition of a proton gradient produced a marked increase in the Na(+)-dependent influx of AIB in NHKE but not in IHKE cells. Competition experiments revealed that the Na(+)-dependent uptake at 50 microM AIB was reduced by neutral alpha-amino acids in the two cell lines. L-Glutamate, L-aspartate, L-arginine and the beta-amino acid taurine had no effect. Only in the IHKE cell line did addition of 5 mM L-lysine produce a slight inhibition. Except for L-proline all of the neutral and acidic amino acids tested reduced the H(+)-dependent uptake of AIB in the IHKE cell line. By contrast, addition of L-aspartate did not influence the transport of AIB in NHKE cells. L-Arginine, but not L-lysine decreased the influx in both cell lines. We conclude that the IHKE cell line has retained the capability to accumulate AIB by transport protein(s) similar to those present for neutral alpha-amino acids in NHKE cells.
我们研究了一种永生化人肾上皮细胞系(IHKE)与正常胚胎细胞(NHKE)相比,是否可作为一种代表性系统来表征人肾近端小管中中性氨基酸的转运。经硫酸镍处理而永生化的IHKE细胞系表现出微绒毛以及高度特化的小管细胞特有的酶标志物。IHKE细胞和NHKE细胞对α-氨基异丁酸(AIB)的钠依赖性摄取是通过具有相同半饱和常数的单一转运系统进行的,但永生化细胞的摄取能力更高。两种类型的细胞中,质子依赖性的AIB内流也由具有相似摄取特征的单一转运成分介导。除了短孵育时间(1分钟)外,施加H⁺梯度会降低AIB的钠依赖性摄取,在短孵育时间时,添加质子梯度会使NHKE细胞中AIB的钠依赖性内流显著增加,但在IHKE细胞中则不然。竞争实验表明,两种细胞系中50微摩尔AIB的钠依赖性摄取会被中性α-氨基酸降低。L-谷氨酸、L-天冬氨酸、L-精氨酸和β-氨基酸牛磺酸没有影响。仅在IHKE细胞系中添加5毫摩尔L-赖氨酸会产生轻微抑制作用。除L-脯氨酸外,所有测试的中性和酸性氨基酸都会降低IHKE细胞系中AIB的质子依赖性摄取。相比之下,添加L-天冬氨酸不会影响NHKE细胞中AIB的转运。L-精氨酸而非L-赖氨酸会降低两种细胞系中的内流。我们得出结论,IHKE细胞系保留了通过与NHKE细胞中存在的中性α-氨基酸转运蛋白相似的转运蛋白积累AIB的能力。