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首页> 外文期刊>Molecular and Cellular Biochemistry >LAT1 overexpression and function compensates downregulation of ASCT2 in an in vitro model of renal proximal tubule cell ageing
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LAT1 overexpression and function compensates downregulation of ASCT2 in an in vitro model of renal proximal tubule cell ageing

机译:在肾近端小管细胞衰老的体外模型中,LAT1的过表达和功能补偿了ASCT2的下调

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Amino acid transporters provide cells neutral amino acids indispensable for growth and proliferation-dependent protein synthesis. This study evaluates whether prolonged serial cell passaging during 6 months (over 50 passages) may induce changes in amino acid transporters properties in Opossum kidney (OK) proximal tubular cells. High passage OK cells exhibit polyploidy, but no difference in the proliferation potential was observed when compared to low passage OK cells. Increased time in culture was accompanied by an increased total, membrane and cytosol protein content. The Na+-insensitive [14C]-l-leucine uptake was promoted almost exclusively thought LAT1 (~ 90 vs 80%, high versus low passage OK cells). The increased LAT1 protein abundance in high passage OK cells correlated positively with enhanced ability to take up [14C]-l-leucine, despite a 4.3-fold decrease in affinity for the substrate. The Na+-sensitive [14C]-l-alanine transport was decreased by 2.5-fold in high passage OK cells. However, no differences in ASCT2 expression were observed between high and low passage OK cells. It is concluded that OK cells show functional differences in both l-leucine and l-alanine uptake as a function of passage time in culture. The increased expression and activity of LAT1 in high passage OK cells may correspond to a mechanism enabling the cell to develop the hypertrophy response to prolonged cell passaging, when the function of ASCT2 is markedly depressed.
机译:氨基酸转运蛋白为细胞提供了生长和增殖依赖性蛋白质合成所必需的中性氨基酸。这项研究评估了在6个月内连续传代的细胞是否经过长时间传代(超过50次传代)是否会导致负鼠肾(OK)近端肾小管细胞的氨基酸转运蛋白特性发生变化。高传代OK细胞表现出多倍性,但与低传代OK细胞相比,未观察到增殖潜能的差异。培养时间的增加伴随着总,膜和胞质蛋白含量的增加。 Na + 不敏感的[ 14 C] -1-亮氨酸的摄取几乎完全是通过LAT1促进的(〜90 vs 80%,高传代与低传代OK细胞)。尽管对底物的亲和力降低了4.3倍,但高传代OK细胞中LAT1蛋白丰度的增加与摄取[ 14 C] -1-亮氨酸的能力增强呈正相关。在高传代OK细胞中,Na + 敏感的[ 14 C] -1-丙氨酸转运减少了2.5倍。但是,高和低传代OK细胞之间没有观察到ASCT2表达的差异。结论是,OK细胞在1-亮氨酸和1-丙氨酸摄取中均显示出功能差异,这与培养物中传代时间有关。当ASCT2的功能显着下降时,高传代OK细胞中LAT1的表达和活性增加可能与使细胞对延长的细胞传代产生肥大反应的机制相对应。

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