Saheki T, Ueda A, Iizima K, Yamada N, Kobayashi K, Takahashi K, Katsunuma T
Clin Chim Acta. 1982 Jan 5;118(1):93-7. doi: 10.1016/0009-8981(82)90230-3.
The activities and kinetic properties of argininosuccinate synthetase in cultured skin fibroblasts of three citrullinemic patients with qualitative or quantitative abnormalities of hepatic argininosuccinate synthetase were examined. The cultured skin fibroblasts of a citrullinemic patient with a low hepatic argininosuccinate synthetase activity showed low activity and abnormal kinetics similar to those of the hepatic enzyme. This suggests a similar genetic origin of the fibroblast argininosuccinate synthetase as of the hepatic enzyme. However, we found normal argininosuccinate synthetase activity in cultured fibroblasts of two citrullinemic patients who had a low hepatic enzyme activity resulting from decrease in the amount of enzyme protein but with normal kinetic properties. This suggests that part of the quantitative abnormality of hepatic argininosuccinate synthetase of citrullinemic patients may be due to an abnormal organ-specific gene expression in the liver.
对三名患有肝脏精氨琥珀酸合成酶定性或定量异常的瓜氨酸血症患者的培养皮肤成纤维细胞中的精氨琥珀酸合成酶活性及动力学特性进行了检测。一名肝脏精氨琥珀酸合成酶活性较低的瓜氨酸血症患者的培养皮肤成纤维细胞显示出低活性和与肝脏酶相似的异常动力学。这表明成纤维细胞精氨琥珀酸合成酶与肝脏酶具有相似的遗传起源。然而,我们发现两名瓜氨酸血症患者的培养成纤维细胞中精氨琥珀酸合成酶活性正常,这两名患者肝脏酶活性较低是由于酶蛋白量减少但动力学特性正常。这表明瓜氨酸血症患者肝脏精氨琥珀酸合成酶的部分定量异常可能是由于肝脏中异常的器官特异性基因表达所致。