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CENP-F 功能丧失导致的小鼠肾脏畸形。

Malformations in the Murine Kidney Caused by Loss of CENP-F Function.

机构信息

Division of Cardiovascular Medicine, Department of Medicine, Vanderbilt University, Nashville, Tennessee.

Institute of Child Health, University College, London, UK.

出版信息

Anat Rec (Hoboken). 2019 Jan;302(1):163-170. doi: 10.1002/ar.24018.

Abstract

Centromere-binding protein F (CENP-F) is a large and complex protein shown to play critical roles in mitosis and various other interphase functions. Previous studies have shown that the disruption of CENP-F function leads to detrimental effects on human development. Still, it is important to note the lack of studies focusing on the effects that the loss of this essential protein may have on specific adult organs. In the current study, we used a novel global knockout murine model to analyze the potential consequences deletion of CENP-F has on adult kidney structure and function. We discovered several structural abnormalities including loss of ciliary structure, tubule dilation, and disruption of the glomerulus. Along with these structural irregularities, renal dysfunction was also detected suggesting hydronephrosis and acute kidney injury in these knockout organs. Importantly, this is the first study linking CENP-F to kidney disease and hopefully these data will serve as a platform to further investigate the molecular mechanisms disrupted in the kidney by the loss of CENP-F. Anat Rec, 302:163-170, 2019. © 2018 Wiley Periodicals, Inc.

摘要

着丝粒结合蛋白 F(CENP-F)是一种大型且复杂的蛋白质,已知其在有丝分裂和其他各种间期功能中发挥关键作用。先前的研究表明,CENP-F 功能的破坏会对人类发育产生有害影响。然而,值得注意的是,缺乏研究关注这种必需蛋白质的缺失可能对特定成年器官产生的影响。在当前的研究中,我们使用了一种新型的全局敲除鼠模型来分析 CENP-F 缺失对成年肾脏结构和功能的潜在后果。我们发现了几种结构异常,包括纤毛结构缺失、小管扩张和肾小球破坏。除了这些结构异常,还检测到肾功能障碍,表明这些敲除器官存在肾盂积水和急性肾损伤。重要的是,这是首次将 CENP-F 与肾脏疾病联系起来的研究,希望这些数据将为进一步研究 CENP-F 缺失导致肾脏中破坏的分子机制提供一个平台。解剖学记录,302:163-170, 2019. © 2018 Wiley Periodicals, Inc.

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