Cheval Lydie, Duong Van Huyen Jean Paul, Bruneval Patrick, Verbavatz Jean-Marc, Elalouf Jean-Marc, Doucet Alain
Laboratoire de Physiologie et Génomique Rénales, Unité Mixte de Recherche Centre National de la Recherche Scientifique/UPMC 7134, Paris, France.
Physiol Genomics. 2004 Sep 16;19(1):61-73. doi: 10.1152/physiolgenomics.00055.2004. Epub 2004 Jul 6.
Plasticity of mouse renal collecting duct in response to potassium depletion.--Renal collecting ducts are the main sites for regulation of whole body potassium balance. Changes in dietary intake of potassium induce pleiotropic adaptations of collecting duct cells, which include alterations of ion and water transport properties along with an hypertrophic response. To study the pleiotropic adaptation of the outer medullary collecting duct (OMCD) to dietary potassium depletion, we combined functional studies of renal function (ion, water, and acid/base handling), analysis of OMCD hypertrophy (electron microscopy) and hyperplasia (PCNA labeling), and large scale analysis of gene expression (transcriptome analysis). The transcriptome of OMCD was compared in mice fed either a normal or a potassium-depleted diet for 3 days using serial analysis of gene expression (SAGE) adapted for downsized extracts. SAGE is based on the generation of transcript-specific tag libraries. Approximately 20,000 tags corresponding to 10,000 different molecular species were sequenced in each library. Among the 186 tags differentially expressed (P < 0.05) between the two libraries, 120 were overexpressed and 66 were downregulated. The SAGE expression profile obtained in the control library was representative of different functional classes of proteins and of the two cell types (principal and alpha-intercalated cells) constituting the OMCD. Combined with gene expression analysis, results of functional and morphological studies allowed us to identify candidate genes for distinct physiological processes modified by potassium depletion: sodium, potassium, and water handling, hyperplasia and hypertrophy. Finally, comparison of mouse and human OMCD transcriptomes allowed us to address the question of the relevance of the mouse as a model for human physiology and pathophysiology.
小鼠肾集合管对钾缺乏的可塑性反应。——肾集合管是调节全身钾平衡的主要部位。饮食中钾摄入量的变化会引起集合管细胞的多效性适应,包括离子和水转运特性的改变以及肥大反应。为了研究外髓集合管(OMCD)对饮食中钾缺乏的多效性适应,我们结合了肾功能的功能研究(离子、水和酸碱处理)、OMCD肥大(电子显微镜)和增生(PCNA标记)分析以及基因表达的大规模分析(转录组分析)。使用适用于小型提取物的基因表达序列分析(SAGE),比较了喂食正常饮食或低钾饮食3天的小鼠的OMCD转录组。SAGE基于转录本特异性标签文库的生成。每个文库中对大约20,000个对应于10,000种不同分子种类的标签进行了测序。在两个文库之间差异表达(P < 0.05)的186个标签中,120个上调,66个下调。在对照文库中获得的SAGE表达谱代表了构成OMCD的不同功能类别的蛋白质以及两种细胞类型(主细胞和α-闰细胞)。结合基因表达分析,功能和形态学研究结果使我们能够识别因钾缺乏而改变的不同生理过程的候选基因:钠、钾和水的处理、增生和肥大。最后,小鼠和人类OMCD转录组的比较使我们能够探讨小鼠作为人类生理学和病理生理学模型的相关性问题。