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黏脂贮积症中黏多糖硫酸酯酶的多种缺陷

Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.

作者信息

Basner R, von Figura K, Glössl J, Klein U, Kresse H, Mlekusch W

出版信息

Pediatr Res. 1979 Dec;13(12):1316-8. doi: 10.1203/00006450-197912000-00002.

Abstract

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.

摘要

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。

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