A microfluidic renal proximal tubule with active reabsorptive function

被引:58
|
作者
Vedula, Else M. [1 ]
Alonso, Jose Luis [2 ,3 ]
Arnaout, M. Amin [2 ,3 ]
Charest, Joseph L. [1 ]
机构
[1] Draper, Biomed Microsyst Grp, Cambridge, MA 02139 USA
[2] Massachusetts Gen Hosp, Leukocyte Biol & Inflammat Program, Dept Med, Nephrol Div, Charlestown, MA 02129 USA
[3] Harvard Med Sch, Charlestown, MA 02129 USA
来源
PLOS ONE | 2017年 / 12卷 / 10期
关键词
MESENCHYMAL STEM-CELLS; ENDOTHELIAL-CELLS; IN-VITRO; BASEMENT-MEMBRANES; GLUCOSE-UPTAKE; SCHWANN-CELLS; SHEAR-STRESS; COCULTURE; MODEL; DIFFERENTIATION;
D O I
10.1371/journal.pone.0184330
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the kidney, the renal proximal tubule (PT) reabsorbs solutes into the peritubular capillaries through active transport. Here, we replicate this reabsorptive function in vitro by engineering a microfluidic PT. The microfluidic PT architecture comprises a porous membrane with user-defined submicron surface topography separating two microchannels representing a PT filtrate lumen and a peritubular capillary lumen. Human PT epithelial cells and microvascular endothelial cells in respective microchannels created a PT-like reabsorptive barrier. Co-culturing epithelial and endothelial cells in the microfluidic architecture enhanced viability, metabolic activity, and compactness of the epithelial layer. The resulting tissue expressed tight junctions, kidney-specific morphology, and polarized expression of kidney markers. The microfluidic PT actively performed sodium-coupled glucose transport, which could be modulated by administration of a sodium-transport inhibiting drug. The microfluidic PT reproduces human physiology at the cellular and tissue levels, and measurable tissue function which can quantify kidney pharmaceutical efficacy and toxicity.
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页数:15
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