Basner R, von Figura K, Glössl J, Klein U, Kresse H, Mlekusch W
Pediatr Res. 1979 Dec;13(12):1316-8. doi: 10.1203/00006450-197912000-00002.
Fibroblasts of four patients affected with mucosulfatidosis (multiple sulfatase deficiency, Austin variant of metachromatic leukodystrophy) were assayed for activities of the five sulfatases known to degrade mucopolysaccharides. These were iduronide 2-sulfate sulfatase, sulfamidase, N-acetyl-galactosamine 6-sulfate sulfatase, arylsulfatase B (N-acetylgalactosamine 4-sulfate sulfatase), and N-acetylglucosamine 6-sulfate sulfatase. The activities of these five sulfatases were severely depressed, thus confirming the known deficiency of arylsulfatase B and the absence of the Hunter and Sanfilippo III A corrective factors that have iduronide 2-sulfate sulfatase and sulfamidase activity, respectively. Together with earlier reports of the deficiencies of arylsulfatases A and C, cholesteryl sulfatase, and dehydroepiandrosterone sulfatae, mucosulfatidosis is now characterized by the deficiency of nine different sulfatases.
对4例患有粘脂贮积症(多种硫酸酯酶缺乏症,异染性脑白质营养不良的奥斯汀变异型)患者的成纤维细胞进行了检测,以测定已知能降解粘多糖的5种硫酸酯酶的活性。这些酶分别是艾杜糖醛酸2-硫酸酯酶、硫酸酰胺酶、N-乙酰半乳糖胺6-硫酸酯酶、芳基硫酸酯酶B(N-乙酰半乳糖胺4-硫酸酯酶)和N-乙酰葡糖胺6-硫酸酯酶。这5种硫酸酯酶的活性严重降低,从而证实了已知的芳基硫酸酯酶B缺乏,以及分别具有艾杜糖醛酸2-硫酸酯酶和硫酸酰胺酶活性的亨特因子和桑菲利波ⅢA型校正因子的缺失。连同先前关于芳基硫酸酯酶A和C、胆固醇硫酸酯酶以及脱氢表雄酮硫酸酯酶缺乏的报道,粘脂贮积症现在的特征是9种不同硫酸酯酶的缺乏。