Olde Hanhof C J A, Dilmen E, Yousef Yengej F A, Latta F, Ammerlaan C M E, Schreurs J, Hooijmaijers L, Jansen J, Rookmaaker M B, Orhon I, Verhaar M C, Hoenderop J G
Department of Molecular Physiology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, Netherlands.
Front Cell Dev Biol. 2023 Jan 25;11:1086823. doi: 10.3389/fcell.2023.1086823. eCollection 2023.
Kidney tubuloids are cell models that are derived from human or mouse renal epithelial cells and show high similarities with their counterparts. Tubuloids grow polarized in 3D, allow for long-term expansion, and represent multiple segments of the nephron, as shown by their gene expression pattern. In addition, human tubuloids form tight, functional barriers and have been succesfully used for drug testing. Our knowledge of mouse tubuloids, on the other hand, is only minimal. In this study, we further characterized mouse tubuloids and differentiated them towards the collecting duct, which led to a significant upregulation of collecting duct-specific mRNAs of genes and protein expression, including the water channel AQP2 and the sodium channel ENaC. Differentiation resulted in polarized expression of collecting duct water channels AQP2 and AQP3. Also, a physiological response to desmopressin and forskolin stimulation by translocation of AQP2 to the apical membrane was demonstrated. Furthermore, amiloride-sensitive ENaC-mediated sodium uptake was shown in differentiated tubuloids using radioactive tracer sodium. This study demonstrates that mouse tubuloids can be differentiated towards the collecting duct and exhibit collecting duct-specific function. This illustrates the potential use of mouse kidney tubuloids as novel models to study (patho)physiology of kidney diseases.
肾小管类器官是源自人或小鼠肾上皮细胞的细胞模型,与它们的对应物具有高度相似性。肾小管类器官在三维空间中呈极性生长,能够长期扩增,并通过其基因表达模式显示出代表肾单位的多个节段。此外,人肾小管类器官形成紧密的功能性屏障,并已成功用于药物测试。另一方面,我们对小鼠肾小管类器官的了解非常有限。在本研究中,我们进一步对小鼠肾小管类器官进行了表征,并将它们诱导分化为集合管,这导致集合管特异性基因的mRNA和蛋白质表达显著上调,包括水通道蛋白AQP2和钠通道ENaC。分化导致集合管水通道蛋白AQP2和AQP3的极性表达。此外,还证明了对去甲加压素和福斯可林刺激的生理反应,即AQP2转位至顶端膜。此外,使用放射性示踪钠在分化的肾小管类器官中显示了氨氯地平敏感的ENaC介导的钠摄取。本研究表明,小鼠肾小管类器官可以分化为集合管并表现出集合管特异性功能。这说明了小鼠肾小管类器官作为研究肾脏疾病(病理)生理学的新型模型的潜在用途。