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来自正常受试者和岩藻糖贮积症患者的培养皮肤成纤维细胞中的α-L-岩藻糖苷酶

alpha-L-fucosidase in cultured skin fibroblasts from normal subjects and fucosidosis patients.

作者信息

Beratis N G, Turner B M, Labadie G, Hirschhorn K

出版信息

Pediatr Res. 1977 Jul;11(7):862-6. doi: 10.1203/00006450-197707000-00017.

Abstract

alpha-L-Fucosidase (EC 3.2.1.51) activity was studied in cultured skin fibroblasts obtained from 23 members of a family in which two cases of fucosidosis type 2 had occurred and in the fibroblasts of a patient with fucosidosis type 1. Both the 4-methylumbelliferyl glycoside and the p-nitrophenyl derivative were used as substrates. pH activity profiles showed two major peaks of activity. With the fluorogenic substrate pH optimum was at 4.5, whereas with the colorigenic substrate maximum activity was at pH 5.7. No activity was found in the fibroblasts of the three patients with the colorimetric assay. With the fluorometric assay the mean activity in the two patients with fucosidosis type 2 was 4.1 and 2.8 (range 1.3-9.9); activity in the patient with fucosidosis type 1 was 4.6 nmol 4-methylumbelliferone/mg protein/hr (range 1.0-8.6). The specific activity in the lysates of the patients' fibroblasts decreased as the amount of cellular protein used per assay increased. Fucosidosis fibroblasts cultured for 3 and 5 days in medium without fetal calf serum showed almost the same levels of apparent residual activity as fibroblasts cultured in medium containing fetal calf serum. Maximum activity in the deficient fibroblasts was at pH 4.5-4.75. Mixing experiments between lysates of both of fucosidosis and a normal fibroblast strain showed the expected enzymatic activities. The mean alpha-fucosidase activity in four heterozygotes for fucosidosis was 37.6 (range 24.1-48.7) and 30.3 (range 19.0-44.1) nmol final product split/mg protein/hr with the fluorogenic and the colorigenic substrate, respectively. In 12 normal fibroblast strains the mean activity +/- SD was 85.3 +/- 24.4 (range 50.8-129.3) and 67.6 +/- 21.1 (range 31.1-118.3). However, in four family members in which the alpha-L-fucosidase phenotype (by isoelectric focusing) was type 2-1, and who should therefore be carrying two normal alleles, the activity was within the heterozygote range. This indicates that occasional overlap between normal subjects and carriers may be present in cultured skin fibroblasts. Increased specific activity of alpha-L-fucosidase at pH 3.2-4.0 was observed after incubation of cell lysates with neuraminidase. The alpha-L-fucosidase activity did not show any increase after fusion between fucosidosis fibroblasts type 1 and 2.

摘要

在一个出现两例2型岩藻糖苷贮积症的家族的23名成员所获取的培养皮肤成纤维细胞中,以及在一名1型岩藻糖苷贮积症患者的成纤维细胞中,研究了α-L-岩藻糖苷酶(EC 3.2.1.51)活性。4-甲基伞形酮糖苷和对硝基苯基衍生物均用作底物。pH活性曲线显示出两个主要活性峰。对于荧光底物,最适pH为4.5,而对于显色底物,最大活性在pH 5.7。用比色法在三名患者的成纤维细胞中未发现活性。用荧光法测定,两名2型岩藻糖苷贮积症患者的平均活性分别为4.1和2.8(范围1.3 - 9.9);1型岩藻糖苷贮积症患者的活性为4.6 nmol 4-甲基伞形酮/mg蛋白/小时(范围1.0 - 8.6)。随着每次测定所用细胞蛋白量的增加,患者成纤维细胞裂解物中的比活性降低。在不含胎牛血清的培养基中培养3天和5天的岩藻糖苷贮积症成纤维细胞,其表观残余活性水平与在含胎牛血清的培养基中培养的成纤维细胞几乎相同。缺陷成纤维细胞中的最大活性在pH 4.5 - 4.75。对岩藻糖苷贮积症患者和成纤维细胞正常菌株的裂解物进行混合实验,显示出预期的酶活性。四名岩藻糖苷贮积症杂合子的平均α-岩藻糖苷酶活性,对于荧光底物和显色底物分别为37.6(范围24.1 - 48.7)和30.3(范围19.0 - 44.1)nmol终产物裂解/mg蛋白/小时。在12个正常成纤维细胞菌株中,平均活性±标准差为85.3±24.4(范围50.8 - 129.3)和67.6±21.1(范围31.1 - 118.3)。然而,在四个α-L-岩藻糖苷酶表型(通过等电聚焦)为2 - 1型、因此应携带两个正常等位基因的家族成员中,其活性处于杂合子范围内。这表明在培养的皮肤成纤维细胞中,正常受试者和携带者之间可能偶尔会出现重叠。用神经氨酸酶孵育细胞裂解物后,观察到在pH 3.2 - 4.0时α-L-岩藻糖苷酶的比活性增加。1型和2型岩藻糖苷贮积症成纤维细胞融合后,α-L-岩藻糖苷酶活性未显示任何增加。

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