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作为研究沃尔曼病模型系统的淋巴样细胞系:酶学、代谢及超微结构研究

Lymphoid cell lines as a model system for the study of Wolman's disease: enzymatic, metabolic and ultrastructural investigations.

作者信息

Nègre A, Salvayre R, Maret A, Vieu C, Bes J C, Borrone C, Durand P, Douste-Blazy L

出版信息

J Inherit Metab Dis. 1986;9(2):193-201. doi: 10.1007/BF01799458.

Abstract

Epstein-Barr virus (EBV) transformed lymphoid cell lines (LCL) were established from blood lymphocytes of a patient affected with Wolman's disease (WD) and from her parents. These LCL showed a severe deficiency in acid lipase activity using every substrate in comparison to LCL from normal subjects, in which acid lipase activity was similar to that in blood lymphocytes. In the LCL from Wolman's disease a major accumulation of neutral lipids was observed, mainly cholesteryl esters, CE (amount around 7 times higher than in normal cells and ratio of esterified/free cholesterol increased by 10 times) and to a lesser extent triglycerides, TG (amount increased by 1.5 times). Electron microscopy showed the storage vacuoles of neutral lipids quite characteristic of this lysosomal disease. The reported data demonstrated the validity of transformed LCL as a cellular model system in culture for experimental studies of Wolman's disease and for investigating the lysosomal metabolism of neutral lipids.

摘要

从一名患沃尔曼病(WD)患者及其父母的血液淋巴细胞中建立了爱泼斯坦-巴尔病毒(EBV)转化的淋巴母细胞系(LCL)。与正常受试者的LCL相比,这些LCL在使用每种底物时酸性脂肪酶活性严重缺乏,而正常受试者的LCL中酸性脂肪酶活性与血液淋巴细胞中的相似。在来自沃尔曼病患者的LCL中,观察到中性脂质大量蓄积,主要是胆固醇酯(CE,含量约比正常细胞高7倍,酯化/游离胆固醇比率增加了10倍),甘油三酯(TG)蓄积程度较轻(含量增加了1.5倍)。电子显微镜显示了这种溶酶体疾病特有的中性脂质储存空泡。报道的数据证明了转化的LCL作为一种细胞模型系统在体外用于沃尔曼病实验研究以及研究中性脂质溶酶体代谢的有效性。

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