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小鼠钠依赖性维生素C转运蛋白Slc23a1和Slc23a2在肾脏发育全过程中的时空微观解剖分布

Temporo-spacial microanatomical distribution of the murine sodium-dependent ascorbic acid transporters Slc23a1 and Slc23a2 in the kidney throughout development.

作者信息

Eck Peter K, Corpe Christopher, Levine Mark A

机构信息

a University of Manitoba, Department of Human Nutritional Sciences, W569 Duff Roblin Building, 190 Dysart Road, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.

b Molecular and Clinical Nutrition Section, Building 10, Room 4D52 MSC 1372, National Institutes of Health, Bethesda, MD 20892-1372, USA.

出版信息

Biochem Cell Biol. 2017 Jun;95(3):421-427. doi: 10.1139/bcb-2015-0090. Epub 2016 Dec 20.

Abstract

The two membrane transporters Slc23a1 and Slc23a2 mediate ascorbic acid uptake into cells. We recently determined the key role of Slc23a1 in renal re-absorption of ascorbic acid in a knockout mouse model. However, the renal spatial and temporal expression patterns of murine Slc23a1 and Slc23a2 are not defined. This study utilizes database evidence combined with experimental confirmation via in-situ hybridization to define the spatial and temporal expression of Slc23a1 in the murine kidney. Slc23a1 is expressed in the early proximal tubule, but not in its precursors during embryonic development, and exclusive proximal tubular expression persists throughout the animal's lifetime. In contrast, Slc23a2 is uniformly expressed in metabolic cell types such as stromal cells. The expression patterns appear to be conserved from rodent lineages to humans.

摘要

两种膜转运蛋白Slc23a1和Slc23a2介导细胞摄取抗坏血酸。我们最近在基因敲除小鼠模型中确定了Slc23a1在肾脏重吸收抗坏血酸中的关键作用。然而,小鼠Slc23a1和Slc23a2在肾脏中的时空表达模式尚未明确。本研究利用数据库证据并通过原位杂交进行实验验证,以确定Slc23a1在小鼠肾脏中的时空表达。Slc23a1在早期近端小管中表达,但在胚胎发育过程中其前体中不表达,并且在动物的整个生命周期中,其在近端小管中的特异性表达持续存在。相比之下,Slc23a2在代谢细胞类型如基质细胞中均匀表达。从啮齿动物谱系到人类,这些表达模式似乎是保守的。

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