Effect of fluid shear stress on in vitro cultured ureteric bud cells
Most kidney cells are continuously exposed to fluid shear stress (FSS) from either blood flow or urine flow. Recent studies suggest that changes in FSS could contribute to the function and injury of these kidney cells. However, it is unclear whether FSS influences kidney development when urinary flo...
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Veröffentlicht in: | Biomicrofluidics 2018-07, Vol.12 (4), p.044107-044107 |
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Sprache: | eng |
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Zusammenfassung: | Most kidney cells are continuously exposed to fluid shear stress (FSS) from either blood
flow or urine flow. Recent studies suggest that changes in FSS could contribute to the
function and injury of these kidney cells. However, it is unclear whether FSS influences
kidney development when urinary flow starts in the embryonic kidneys. In this study, we
evaluated the influence of FSS on in vitro cultured ureteric bud (UB)
cells by using a pumpless microfluidic device, which offers the convenience of conducting
parallel cell culture experiments while also eliminating the need for cumbersome
electronic driven equipment and intricate techniques. We first validated the function of
the device by both mathematical model and experimental measurements. UB cells dissected
from E15.5 mouse embryonic kidneys were cultured in the pumpless microfluidic device and
subjected to FSS in the range of 0.4–0.6 dyn mm−2 for 48 h (dynamic). Control
UB cells were similarly cultured in the device and maintained under a no-flow condition
(static). We found from our present study that the exposure to FSS for up to 48 h led to
an increase in mRNA expression levels of UB tip cell marker genes (Wnt11,
Ret, Etv4) with a decrease in stalk cell marker genes
(Wnt7b, Tacstd2). In further support of the enrichment
of UB tip cell population in response to FSS, we also found that exposure to FSS led to a
remarkable reduction in the binding of lectin Dolichos Biflorus Agglutinin. In conclusion,
results of our present study show that exposure to FSS led to an enrichment in UB tip cell
populations, which could contribute to the development and function of the embryonic
kidney when urine flow starts at around embryonic age E15.5 in mouse. Since UB tip cells
are known to be the proliferative progenitor cells that contribute to the branching
morphogenesis of the collecting system in the kidney, our finding could imply an important
link between the FSS from the initiation of urine flow and the development and function of
the kidney. |
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ISSN: | 1932-1058 1932-1058 |
DOI: | 10.1063/1.5035328 |