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皮质厚升支的简史:系统生物学视角

A brief history of the cortical thick ascending limb: a systems-biology perspective.

作者信息

Sohail Shahzad K, Jayatissa Nipun U, Mejia Raymond, Khan Shaza, Chou Chung-Lin, Yang Chin-Rang, Knepper Mark A

机构信息

Epithelial Systems Biology Laboratory, Systems Biology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States.

出版信息

Am J Physiol Renal Physiol. 2025 Jan 1;328(1):F82-F94. doi: 10.1152/ajprenal.00243.2024. Epub 2024 Nov 19.

Abstract

Here, we review key events in the accrual of knowledge about the cortical thick ascending limb (CTAL) of the kidney, starting with its initial characterization by Maurice Burg in 1973. Burg's work showed that the CTAL actively reabsorbs NaCl and that, because its water permeability is virtually zero, it can lower the luminal NaCl concentration to a "static head" level well below blood levels. This process is central to the kidney's ability to excrete dilute urine in states of high water intake. Following Burg's original observations, Greger and Schlatter, working in the 1980s, identified the membrane transport processes responsible for transepithelial NaCl transport in the CTAL. In the 1990s, several investigators identified the key transporter genes and proteins at a molecular level by cDNA cloning. The successful completion of human and mouse genome sequencing projects at the turn of the century led to the development of transcriptomic and proteomic methodologies that allowed the identification of complete transcriptomes and proteomes of CTAL cells. Knowledge accrual was enhanced by the development of differential equation-based models of transport in the CTAL in the 2010s. Here, we used a simplified mathematical model of NaCl ("salt"), urea, and water transport in the CTAL to address three key questions about CTAL function: ) What is the mechanism of Burg's "static head" phenomenon? ) How does the kidney compensate for the very short length of the CTALs of juxtamedullary nephrons? ) Which of the three isoforms of the apical Na-K-2Cl cotransporter (NKCC2) dominates functionally in the CTAL? Here, we review key events in the accrual of knowledge about the cortical thick ascending limb (CTAL) of the kidney, starting with its initial characterization by Maurice Burg in 1973, and culminating with the application of systems biology techniques including mathematical modeling.

摘要

在此,我们回顾了有关肾皮质厚升支(CTAL)知识积累过程中的关键事件,始于1973年莫里斯·伯格对其的初步描述。伯格的研究表明,CTAL能主动重吸收氯化钠,并且由于其水通透性几乎为零,它能将管腔内氯化钠浓度降低至远低于血液水平的“静水压头”水平。这一过程对于肾脏在高水摄入状态下排泄稀释尿液的能力至关重要。继伯格最初的观察之后,20世纪80年代,格雷格和施拉特确定了CTAL中负责跨上皮氯化钠转运的膜转运过程。20世纪90年代,几位研究人员通过cDNA克隆在分子水平上鉴定了关键转运蛋白基因和蛋白质。世纪之交人类和小鼠基因组测序项目的成功完成,促成了转录组学和蛋白质组学方法的发展,从而能够鉴定CTAL细胞的完整转录组和蛋白质组。21世纪10年代基于微分方程的CTAL转运模型的发展进一步推动了知识的积累。在此,我们使用CTAL中氯化钠(“盐”)、尿素和水转运的简化数学模型来解决关于CTAL功能的三个关键问题:1)伯格“静水压头”现象的机制是什么?2)肾脏如何补偿近髓肾单位CTAL极短的长度?3)顶端钠 - 钾 - 2氯共转运体(NKCC2)的三种同工型中哪一种在CTAL功能上占主导地位?在此,我们回顾了有关肾皮质厚升支(CTAL)知识积累过程中的关键事件,始于1973年莫里斯·伯格对其的初步描述,并以包括数学建模在内的系统生物学技术的应用为高潮。

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