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胱氨酸病的发病机制:胱氨酸蓄积以外的机制。

The pathogenesis of cystinosis: mechanisms beyond cystine accumulation.

机构信息

Dept. of Pediatric Nephrology, Univ. Hospitals Leuven, Herestraat 49, 3000 Leuven, Belgium.

出版信息

Am J Physiol Renal Physiol. 2010 Nov;299(5):F905-16. doi: 10.1152/ajprenal.00318.2010. Epub 2010 Sep 8.

Abstract

Renal proximal tubules are highly sensitive to ischemic and toxic insults and are affected in diverse genetic disorders, of which nephropathic cystinosis is the most common. The disease is caused by mutations in the CTNS gene, encoding the lysosomal cystine transporter cystinosin, and is characterized by accumulation of cystine in the lysosomes throughout the body. In the majority of the patients, this leads to generalized proximal tubular dysfunction (also called DeToni-Debré-Fanconi syndrome) in the first year and progressive renal failure during the first decade. Extrarenal organs are affected by cystinosis as well, with clinical symptoms manifesting mostly after 10 yr of age. The cystine-depleting agent cysteamine significantly improves life expectancy of patients with cystinosis, but offers no cure, pointing to the complexity of the disease mechanism. In this review, current knowledge on the pathogenesis of cystinosis is described and placed in perspective of future research.

摘要

肾近端小管对缺血和毒性损伤非常敏感,并且受多种遗传疾病的影响,其中最常见的是遗传性胱氨酸贮积症。该疾病是由编码溶酶体胱氨酸转运蛋白胱氨酸酶的 CTNS 基因突变引起的,其特征是胱氨酸在全身溶酶体中积累。在大多数患者中,这会导致第一年全身近端肾小管功能障碍(也称为 DeToni-Debré-Fanconi 综合征),并在第一个十年期间进展为肾衰竭。胱氨酸贮积症也会影响肾脏外器官,其临床症状主要在 10 岁后出现。耗竭胱氨酸的药物半胱氨酸显著改善了胱氨酸贮积症患者的预期寿命,但并不能治愈该疾病,这表明该疾病的发病机制非常复杂。在这篇综述中,描述了胱氨酸贮积症发病机制的现有知识,并展望了未来的研究方向。

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