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谷胱甘肽前体可补充胱氨酸病细胞系中减少的谷胱甘肽池。

Glutathione precursors replenish decreased glutathione pool in cystinotic cell lines.

作者信息

Chol Marie, Nevo Nathalie, Cherqui Stéphanie, Antignac Corinne, Rustin Pierre

机构信息

INSERM U574, Néphropathies Héréditaires et Rein en Développement, Hôpital Necker-Enfants Malades, rue de Sèvres, 75015 Paris, France.

出版信息

Biochem Biophys Res Commun. 2004 Nov 5;324(1):231-5. doi: 10.1016/j.bbrc.2004.09.033.

Abstract

Cystinosis is an inherited disorder due to mutations in the CTNS gene which encodes cystinosin, a lysosomal transmembrane protein involved in cystine export to the cytosol. Both accumulation of cystine in the lysosome and decreased cystine in the cytosol may participate in the pathogenic mechanism underlying the disease. We observed that cystinotic cell lines have moderate decrease of glutathione content during exponential growth phase. This resulted in increased solicitation of oxidative defences of the cell denoted by concurrent superoxide dismutase induction, although without major oxidative insult under our experimental conditions. Finally, decreased glutathione content in cystinotic cell lines could be counterbalanced by a series of exogenous precursors of cysteine, denoting that lysosomal cystine export is a natural source of cellular cysteine in the studied cell lines.

摘要

胱氨酸贮积症是一种遗传性疾病,由CTNS基因突变所致,该基因编码胱氨酸转运体,这是一种参与将胱氨酸转运至胞质溶胶的溶酶体跨膜蛋白。胱氨酸在溶酶体中的蓄积以及胞质溶胶中胱氨酸的减少均可能参与该疾病的致病机制。我们观察到,胱氨酸贮积症细胞系在指数生长期谷胱甘肽含量有中度降低。这导致细胞氧化防御的应激增加,表现为同时诱导超氧化物歧化酶,尽管在我们的实验条件下没有严重的氧化损伤。最后,胱氨酸贮积症细胞系中谷胱甘肽含量的降低可被一系列半胱氨酸外源性前体所抵消,这表明在研究的细胞系中,溶酶体胱氨酸转运是细胞半胱氨酸的天然来源。

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