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肾近端小管中的氯离子转运体与受体介导的内吞作用

Chloride transporters and receptor-mediated endocytosis in the renal proximal tubule.

作者信息

Devuyst Olivier, Luciani Alessandro

机构信息

Institute of Physiology, Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.

出版信息

J Physiol. 2015 Sep 15;593(18):4151-64. doi: 10.1113/JP270087. Epub 2015 May 11.

Abstract

KEY POINTS

The reabsorptive activity of renal proximal tubule cells is mediated by receptor-mediated endocytosis and polarized transport systems that reflect final cell differentiation. Loss-of-function mutations of the endosomal chloride-proton exchanger ClC-5 (Dent's disease) cause a major trafficking defect in proximal tubule cells, associated with lysosomal dysfunction, oxidative stress and dedifferentiation/proliferation. A similar but milder defect is associated with mutations in CFTR (cystic fibrosis transmembrane conductance regulator). Vesicular chloride transport appears to be important for the integrity of the endolysosomal pathway in epithelial cells.

ABSTRACT

The epithelial cells lining the proximal tubules of the kidney reabsorb a large amount of filtered ions and solutes owing to receptor-mediated endocytosis and polarized transport systems that reflect final cell differentiation. Dedifferentiation of proximal tubule cells and dysfunction of receptor-mediated endocytosis characterize Dent's disease, a rare disorder caused by inactivating mutations in the CLCN5 gene that encodes the endosomal chloride-proton exchanger, ClC-5. The disease is characterized by a massive urinary loss of solutes (renal Fanconi syndrome), with severe metabolic complications and progressive renal failure. Investigations of mutations affecting the gating of ClC-5 revealed that the proximal tubule dysfunction may occur despite normal endosomal acidification. In addition to defective endocytosis, proximal tubule cells lacking ClC-5 show a trafficking defect in apical receptors and transporters, as well as lysosomal dysfunction and typical features of dedifferentiation, proliferation and oxidative stress. A similar but milder defect is observed in mouse models with defective CFTR, a chloride channel that is also expressed in the endosomes of proximal tubule cells. These data suggest a major role for endosomal chloride transport in the maintenance of epithelial differentiation and reabsorption capacity of the renal proximal tubule.

摘要

关键点

肾近端小管细胞的重吸收活性由受体介导的内吞作用和反映最终细胞分化的极化转运系统介导。内体氯化物-质子交换体ClC-5(丹特病)的功能丧失突变导致近端小管细胞出现主要的转运缺陷,伴有溶酶体功能障碍、氧化应激和去分化/增殖。类似但较轻的缺陷与囊性纤维化跨膜电导调节因子(CFTR)的突变有关。囊泡氯化物转运似乎对上皮细胞内溶酶体途径的完整性很重要。

摘要

肾近端小管内衬的上皮细胞由于受体介导的内吞作用和反映最终细胞分化的极化转运系统,重吸收大量滤过的离子和溶质。近端小管细胞的去分化和受体介导的内吞功能障碍是丹特病的特征,丹特病是一种罕见的疾病,由编码内体氯化物-质子交换体ClC-5的CLCN5基因的失活突变引起。该疾病的特征是溶质大量尿流失(肾范科尼综合征),伴有严重的代谢并发症和进行性肾衰竭。对影响ClC-5门控的突变的研究表明,尽管内体酸化正常,近端小管功能障碍仍可能发生。除了内吞缺陷外,缺乏ClC-5的近端小管细胞在顶端受体和转运体中表现出转运缺陷,以及溶酶体功能障碍和去分化、增殖和氧化应激的典型特征。在CFTR缺陷的小鼠模型中观察到类似但较轻的缺陷,CFTR是一种也在近端小管细胞的内体中表达的氯通道。这些数据表明内体氯化物转运在维持肾近端小管上皮细胞分化和重吸收能力方面起主要作用。

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