| Literature DB >> 35484146 |
Mohammad Ikbal Choudhury1,2, Yizeng Li1,3, Panagiotis Mistriotis4,5, Ana Carina N Vasconcelos1,2, Eryn E Dixon6,7,8, Jing Yang1,2, Morgan Benson2,4, Debonil Maity2,4, Rebecca Walker6,8, Leigha Martin4, Fatima Koroma4, Feng Qian6,8, Konstantinos Konstantopoulos2,4, Owen M Woodward7,8, Sean X Sun9,10.
Abstract
The role of mechanical forces driving kidney epithelial fluid transport and morphogenesis in kidney diseases is unclear. Here, using a microfluidic platform to recapitulate fluid transport activity of kidney cells, we report that renal epithelial cells can actively generate hydraulic pressure gradients across the epithelium. The fluidic flux declines with increasing hydraulic pressure until a stall pressure, in a manner similar to mechanical fluid pumps. For normal human kidney cells, the fluidic flux is from apical to basal, and the pressure is higher on the basal side. For human Autosomal Dominant Polycystic Kidney Disease cells, the fluidic flux is reversed from basal to apical. Molecular and proteomic studies reveal that renal epithelial cells are sensitive to hydraulic pressure gradients, changing gene expression profiles and spatial arrangements of ion exchangers and the cytoskeleton in different pressure conditions. These results implicate mechanical force and hydraulic pressure as important variables during kidney function and morphological change, and provide insights into pathophysiological mechanisms underlying the development and transduction of hydraulic pressure gradients.Entities:
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Year: 2022 PMID: 35484146 PMCID: PMC9050750 DOI: 10.1038/s41467-022-29988-w
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694