Chambers Brooke E, Weaver Nicole E, Lara Caroline M, Nguyen Thanh Khoa, Wingert Rebecca A
Department of Biological Sciences, Center for Stem Cells and Regenerative Medicine, Center for Zebrafish Research, Boler-Parseghian Center for Rare and Neglected Diseases, Warren Center for Drug Discovery, University of Notre Dame, Notre Dame, Indiana (IN), USA.
Tissue Barriers. 2024 Apr 2;12(2):2219605. doi: 10.1080/21688370.2023.2219605. Epub 2023 May 31.
Kidney disease is a devastating condition affecting millions of people worldwide, where over 100,000 patients in the United States alone remain waiting for a lifesaving organ transplant. Concomitant with a surge in personalized medicine, single-gene mutations, and polygenic risk alleles have been brought to the forefront as core causes of a spectrum of renal disorders. With the increasing prevalence of kidney disease, it is imperative to make substantial strides in the field of kidney genetics. Nephrons, the core functional units of the kidney, are epithelial tubules that act as gatekeepers of body homeostasis by absorbing and secreting ions, water, and small molecules to filter the blood. Each nephron contains a series of proximal and distal segments with explicit metabolic functions. The embryonic zebrafish provides an ideal platform to systematically dissect the genetic cues governing kidney development. Here, we review the use of zebrafish to discover nephrogenesis genes.
肾脏疾病是一种毁灭性的疾病,影响着全球数百万人,仅在美国就有超过10万名患者等待救命的器官移植。随着个性化医疗的兴起,单基因突变和多基因风险等位基因已成为一系列肾脏疾病的核心病因,被置于前沿位置。随着肾脏疾病患病率的不断上升,在肾脏遗传学领域取得重大进展势在必行。肾单位是肾脏的核心功能单位,是上皮小管,通过吸收和分泌离子、水和小分子来过滤血液,从而充当身体内环境稳态的守门人。每个肾单位都包含一系列具有明确代谢功能的近端和远端节段。胚胎斑马鱼为系统剖析控制肾脏发育的遗传线索提供了一个理想的平台。在此,我们综述了利用斑马鱼发现肾发生基因的情况。