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半乳糖野尻霉素衍生物可恢复在酶缺陷型基因敲除小鼠成纤维细胞中表达的突变型人β-半乳糖苷酶活性。

Galactonojirimycin derivatives restore mutant human beta-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse.

作者信息

Tominaga L, Ogawa Y, Taniguchi M, Ohno K, Matsuda J, Oshima A, Suzuki Y, Nanba E

机构信息

Gene Research Center, Tottori University, 86 Nishimachi, Yonago 683-8503, Japan.

出版信息

Brain Dev. 2001 Aug;23(5):284-7. doi: 10.1016/s0387-7604(01)00216-9.

Abstract

Ten low molecular compounds analogous to galactose were screened for inhibition of human beta-galactosidase activity. Among them, 1-deoxy-galactonojirimycin and N-(n-butyl)-deoxy-galactonojirimycin showed an inhibitory effect at high concentrations. However, they restored mutant enzyme activities expressed in enzyme-deficient knockout mouse fibroblasts and human beta-galactosidosis fibroblasts at lower intracellular concentrations. This effect was more remarkable on G(M1)-gangliosidosis mutations (R201C, I51T, R201H, R457Q) than Morquio B disease mutations (W273L, Y83H). These low molecular compounds pass though the blood-brain barrier in mice. We hope that this new therapeutic approach will become clinically applicable in the near future.

摘要

筛选了十种与半乳糖类似的低分子化合物,以检测其对人β-半乳糖苷酶活性的抑制作用。其中,1-脱氧-半乳糖野尻霉素和N-(正丁基)-脱氧-半乳糖野尻霉素在高浓度时表现出抑制作用。然而,在较低的细胞内浓度下,它们能恢复在酶缺陷型基因敲除小鼠成纤维细胞和人β-半乳糖苷沉积症成纤维细胞中表达的突变酶活性。这种作用在GM1神经节苷脂沉积症突变(R201C、I51T、R201H、R457Q)中比莫尔基奥氏综合征B型疾病突变(W273L、Y83H)更为显著。这些低分子化合物可穿过小鼠的血脑屏障。我们希望这种新的治疗方法在不久的将来能应用于临床。

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