scholarly journals Cdc42 activation couples fluid shear stress to apical endocytosis in proximal tubule cells

2017 ◽  
Vol 5 (19) ◽  
pp. e13460 ◽  
Author(s):  
Sohinee Bhattacharyya ◽  
Frédéric G. Jean-Alphonse ◽  
Venkatesan Raghavan ◽  
Jennifer C. McGarvey ◽  
Youssef Rbaibi ◽  
...  
2018 ◽  
Vol 32 (S1) ◽  
Author(s):  
Qidong Ren ◽  
Megan L. Eshbach ◽  
Natalie L. Rittenhouse ◽  
Kimberly R. Long ◽  
Youssef Rbaibi ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Emily J. Ross ◽  
Emily R. Gordon ◽  
Hanna Sothers ◽  
Roshan Darji ◽  
Oakley Baron ◽  
...  

AbstractThe kidney proximal tubule is the primary site for solute reabsorption, secretion and where kidney diseases can originate, including drug-induced toxicity. Two-dimensional cell culture systems of the human proximal tubule cells (hPTCs) are often used to study these processes. However, these systems fail to model the interplay between filtrate flow, fluid shear stress (FSS), and functionality essential for understanding renal diseases and drug toxicity. The impact of FSS exposure on gene expression and effects of FSS at differing rates on gene expression in hPTCs has not been thoroughly investigated. Here, we performed RNA-sequencing of human RPTEC/TERT1 cells in a microfluidic chip-based 3D model to determine transcriptomic changes. We measured transcriptional changes following treatment of cells in this device at three different fluidic shear stress. We observed that FSS changes the expression of PTC-specific genes and impacted genes previously associated with renal diseases in genome-wide association studies (GWAS). At a physiological FSS level, we observed cell morphology, enhanced polarization, presence of cilia, and transport functions using albumin reabsorption via endocytosis and efflux transport. Here, we present a dynamic view of hPTCs response to FSS with increasing fluidic shear stress conditions and provide insight into hPTCs cellular function under biologically relevant conditions.


2017 ◽  
Vol 28 (19) ◽  
pp. 2508-2517 ◽  
Author(s):  
Kimberly R. Long ◽  
Katherine E. Shipman ◽  
Youssef Rbaibi ◽  
Elizabeth V. Menshikova ◽  
Vladimir B. Ritov ◽  
...  

Cells lining the proximal tubule (PT) have unique membrane specializations that are required to maintain the high-capacity ion transport and endocytic functions of this nephron segment. PT cells in vivo acutely regulate ion transport in response to changes in glomerular filtration rate (GFR) to maintain glomerulotubular balance. PT cells in culture up-regulate endocytic capacity in response to acute changes in fluid shear stress (FSS); however, it is not known whether GFR modulates PT endocytosis to enable maximally efficient uptake of filtered proteins in vivo. Here, we show that cells cultured under continuous FSS develop an expanded apical endocytic pathway and increased endocytic capacity and lysosomal biogenesis. Furthermore, endocytic capacity in fully differentiated cells is rapidly modulated by changes in FSS. PT cells exposed to continuous FSS also acquired an extensive brush border and basolateral membrane invaginations resembling those observed in vivo. Culture under suboptimal levels of FSS led to intermediate phenotypes, suggesting a threshold effect. Cells exposed to FSS expressed higher levels of key proteins necessary for PT function, including ion transporters, receptors, and membrane-trafficking machinery, and increased adenine nucleotide levels. Inhibition of the mechanistic target of rapamycin (mTOR) using rapamycin prevented the increase in cellular energy levels, lysosomal biogenesis, and endocytic uptake, suggesting that these represent a coordinated differentiation program. In contrast, rapamycin did not prevent the FSS-induced increase in Na+/K+-ATPase levels. Our data suggest that rapid tuning of the endocytic response by changes in FSS may contribute to glomerulotubular balance in vivo. Moreover, FSS provides an essential stimulus in the differentiation of PT cells via separate pathways that up-regulate endocytosis and ion transport capacity. Variations in FSS may also contribute to the maturation of PT cells during kidney development and during repair after kidney injury.


2017 ◽  
Vol 31 (5) ◽  
pp. 1796-1806 ◽  
Author(s):  
Sami G. Mohammed ◽  
Francisco J. Arjona ◽  
Femke Latta ◽  
René J. M. Bindels ◽  
Ronald Roepman ◽  
...  

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