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戈谢病II型。正常组织和戈谢组织中β-葡萄糖苷酶动力学及牛磺胆酸钠作用的研究。

Gaucher's disease II. Studies on the kinetics of beta-glucosidase and the effects of sodium taurocholate in normal and Gaucher tissues.

作者信息

Choy F Y, Davidson R G

出版信息

Pediatr Res. 1980 Jan;14(1):54-9. doi: 10.1203/00006450-198001000-00013.

Abstract

beta-Glucosidase activity from normal human cultured fibroblasts was not affected by the presence of up to 0.1% (w/v) (1.86 mM) purified sodium taurocholate. At concentrations greater than 0.1%, there was a gradual decrease in activity. Conversely, beta-glucosidase activity from fibroblasts of three patients with juvenile onset Gaucher's disease was preferentially inhibited by the detergent at concentrations as low as 0.025% (0.46 mM). A 40% decrease in activity was observed at 0.1%. Crude sodium taurocholate was more potent in inhibiting beta-glucosidase activity from both the normal and Gaucher fibroblasts. However, very high background fluorescence and inconsistent results were observed when different batches of the crude taurocholate from the same or different sources were used. Similarly, beta-glucosidase activity from Gaucher splenic tissue homogenates, supernatant fluids (40,000 x g) and residue pellets was preferentially inhibited by purified sodium taurocholate. These findings indicate that the reliability and sensitivity of the enzyme assay for Gaucher's disease can be enhanced by determining beta-glucosidase activity in both the absence and presence of purified sodium taurocholate, particularly when variant cases with relatively high residual enzyme activity are encountered. In contrast to the enzyme from fibroblasts and spleens, beta-glucosidase activity from human placenta was markedly activated (greater than 300%) by the presence of 0.08% (1.49 mM) purified sodium taurocholate or 0.1 mM phosphatidyl serine, suggesting the presence of a predominate form of beta-glucosidase, possibly glucocerebroside beta-glucosidase, which is activated by the detergent. The apparent Michaelis constant (Km) for both the soluble and membrane-bound enzyme from normal fibroblasts was 1.6 +/- 0.1 mM. Kms from a patient with severe juvenile Gaucher's disease and two other patients with milder manifestations were 0.8 +/- 0.2 and 3.3 +/- 0.3 mM, respectively.

摘要

高达0.1%(w/v)(1.86 mM)的纯化牛磺胆酸钠的存在不会影响正常人培养成纤维细胞的β-葡萄糖苷酶活性。浓度高于0.1%时,活性逐渐降低。相反,三名青少年型戈谢病患者的成纤维细胞中的β-葡萄糖苷酶活性在低至0.025%(0.46 mM)的去污剂浓度下就受到优先抑制。在0.1%时观察到活性降低了40%。粗制牛磺胆酸钠在抑制正常和戈谢病成纤维细胞的β-葡萄糖苷酶活性方面更有效。然而,当使用来自相同或不同来源的不同批次的粗制牛磺胆酸钠时,观察到非常高的背景荧光和不一致的结果。同样,纯化的牛磺胆酸钠优先抑制戈谢病脾脏组织匀浆、上清液(40,000×g)和残留沉淀中的β-葡萄糖苷酶活性。这些发现表明,通过在有无纯化牛磺胆酸钠的情况下测定β-葡萄糖苷酶活性,可以提高戈谢病酶测定的可靠性和敏感性,特别是当遇到具有相对较高残留酶活性的变异病例时。与来自成纤维细胞和脾脏的酶相反,0.08%(1.49 mM)的纯化牛磺胆酸钠或0.1 mM磷脂酰丝氨酸的存在可使来自人胎盘的β-葡萄糖苷酶活性显著激活(大于300%),这表明存在一种主要形式的β-葡萄糖苷酶,可能是葡糖脑苷脂β-葡萄糖苷酶,它被去污剂激活。正常成纤维细胞的可溶性和膜结合酶的表观米氏常数(Km)为1.6±0.1 mM。一名严重青少年型戈谢病患者和另外两名症状较轻患者的Km分别为0.8±0.2和3.3±0.3 mM。

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