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培养的皮肤成纤维细胞:对威尔逊病的诊断有用吗?

Cultured skin fibroblasts: useful for diagnosis of Wilson's disease?

作者信息

Van den Berg G J, Van den Hamer C J, Meijer R J, Hoogenraad T U

机构信息

Interfaculty Reactor Institute, Delft University of Technology, The Netherlands.

出版信息

J Inherit Metab Dis. 1989;12(1):64-71. doi: 10.1007/BF01805532.

Abstract

The copper content of and radiocopper uptake in fibroblast cultures were studied to evaluate their usefulness for the diagnosis of Wilson's disease. We used methods closely related to those described in the literature, and applied these to cell lines of six patients with Wilson's disease and 12 controls. The results were: (1) The copper content of the cytosol of skin fibroblasts derived from patients with Wilson's disease was lower than that of controls when the cells were grown in a medium with a low copper concentration (0.7 mumolL-1); increased copper concentration (157 mumol L-1 in the medium failed to demonstrate any difference between normal fibroblasts and those derived from patients with Wilson's disease. (2) Radiocopper uptake studies did not differentiate between normal fibroblasts and fibroblasts from patients with Wilson's disease. We conclude that the cytosolic copper content of fibroblasts grown in a low copper medium is a potential diagnostic tool in Wilson's disease. At present not all controls can be distinguished from the Wilson cells; ways must be sought, therefore, of improving the technique.

摘要

研究了成纤维细胞培养物中的铜含量和放射性铜摄取情况,以评估其对威尔逊病诊断的实用性。我们采用了与文献中描述密切相关的方法,并将其应用于6例威尔逊病患者和12例对照的细胞系。结果如下:(1)当细胞在低铜浓度(0.7μmol/L)的培养基中生长时,威尔逊病患者皮肤成纤维细胞胞质溶胶中的铜含量低于对照组;增加铜浓度(培养基中为157μmol/L)未能显示正常成纤维细胞与威尔逊病患者来源的成纤维细胞之间有任何差异。(2)放射性铜摄取研究无法区分正常成纤维细胞和威尔逊病患者的成纤维细胞。我们得出结论,在低铜培养基中生长的成纤维细胞的胞质铜含量是威尔逊病的一种潜在诊断工具。目前并非所有对照都能与威尔逊病细胞区分开来;因此,必须寻求改进该技术的方法。

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