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胱氨酸病中的肾范可尼综合征:发病机制的见解和治疗观点。

The renal Fanconi syndrome in cystinosis: pathogenic insights and therapeutic perspectives.

机构信息

Department of Pediatrics, Division of Genetics, University of California San Diego, 9500 Gilman Drive, MC 0734, La Jolla, California 92093-0734, USA.

Cell biology, de Duve Institute and Université catholique de Louvain, UCL-Brussels, 75 Avenue Hippocrate, B-1200 Brussels, Belgium.

出版信息

Nat Rev Nephrol. 2017 Feb;13(2):115-131. doi: 10.1038/nrneph.2016.182. Epub 2016 Dec 19.

Abstract

Cystinosis is an autosomal recessive metabolic disease that belongs to the family of lysosomal storage disorders. It is caused by a defect in the lysosomal cystine transporter, cystinosin, which results in an accumulation of cystine in all organs. Despite the ubiquitous expression of cystinosin, a renal Fanconi syndrome is often the first manifestation of cystinosis, usually presenting within the first year of life and characterized by the early and severe dysfunction of proximal tubule cells, highlighting the unique vulnerability of this cell type. The current therapy for cystinosis, cysteamine, facilitates lysosomal cystine clearance and greatly delays progression to kidney failure but is unable to correct the Fanconi syndrome. This Review summarizes decades of studies that have fostered a better understanding of the pathogenesis of the renal Fanconi syndrome associated with cystinosis. These studies have unraveled some of the early molecular changes that occur before the onset of tubular atrophy and identified a role for cystinosin beyond cystine transport, in endolysosomal trafficking and proteolysis, lysosomal clearance, autophagy and the regulation of energy balance. These studies have also led to the identification of new potential therapeutic targets and here, we outline the potential role of stem cell therapy for cystinosis and provide insights into the mechanism of haematopoietic stem cell-mediated kidney protection.

摘要

胱氨酸贮积症是一种常染色体隐性遗传代谢疾病,属于溶酶体贮积症家族。它是由溶酶体胱氨酸转运蛋白胱氨酸酶缺陷引起的,导致胱氨酸在所有器官中积累。尽管胱氨酸酶广泛表达,但胱氨酸贮积症患者常首先出现肾脏范可尼综合征,通常在生命的第一年出现,其特征为近端肾小管细胞的早期和严重功能障碍,突出了这种细胞类型的独特脆弱性。目前胱氨酸贮积症的治疗药物半胱氨酸可促进溶酶体胱氨酸清除,并大大延缓肾衰竭的进展,但无法纠正范可尼综合征。这篇综述总结了几十年来的研究成果,这些研究促进了对与胱氨酸贮积症相关的肾脏范可尼综合征发病机制的更好理解。这些研究揭示了在管状萎缩发生之前发生的一些早期分子变化,并确定了胱氨酸酶除了胱氨酸转运以外,在溶酶体运输和蛋白水解、溶酶体清除、自噬和能量平衡调节中的作用。这些研究还导致了新的潜在治疗靶点的鉴定,在这里,我们概述了用于胱氨酸贮积症的干细胞治疗的潜在作用,并深入了解了造血干细胞介导的肾脏保护的机制。

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