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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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Autores principales: Kimura, Hiroshi, Nishikawa, Masaki, Yanagawa, Naomi, Nakamura, Hiroko, Miyamoto, Shunsuke, Hamon, Morgan, Hauser, Peter, Zhao, Lifu, Jo, Oak D., Komeya, Mitsuru, Ogawa, Takehiko, Yanagawa, Norimoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039298/
https://www.ncbi.nlm.nih.gov/pubmed/30034570
http://dx.doi.org/10.1063/1.5035328
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author Kimura, Hiroshi
Nishikawa, Masaki
Yanagawa, Naomi
Nakamura, Hiroko
Miyamoto, Shunsuke
Hamon, Morgan
Hauser, Peter
Zhao, Lifu
Jo, Oak D.
Komeya, Mitsuru
Ogawa, Takehiko
Yanagawa, Norimoto
author_facet Kimura, Hiroshi
Nishikawa, Masaki
Yanagawa, Naomi
Nakamura, Hiroko
Miyamoto, Shunsuke
Hamon, Morgan
Hauser, Peter
Zhao, Lifu
Jo, Oak D.
Komeya, Mitsuru
Ogawa, Takehiko
Yanagawa, Norimoto
author_sort Kimura, Hiroshi
collection PubMed
description 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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spelling pubmed-60392982018-07-20 Effect of fluid shear stress on in vitro cultured ureteric bud cells Kimura, Hiroshi Nishikawa, Masaki Yanagawa, Naomi Nakamura, Hiroko Miyamoto, Shunsuke Hamon, Morgan Hauser, Peter Zhao, Lifu Jo, Oak D. Komeya, Mitsuru Ogawa, Takehiko Yanagawa, Norimoto Biomicrofluidics Regular Articles 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. AIP Publishing LLC 2018-07-10 /pmc/articles/PMC6039298/ /pubmed/30034570 http://dx.doi.org/10.1063/1.5035328 Text en © 2018 Author(s). 1932-1058/2018/12(4)/044107/10 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Articles
Kimura, Hiroshi
Nishikawa, Masaki
Yanagawa, Naomi
Nakamura, Hiroko
Miyamoto, Shunsuke
Hamon, Morgan
Hauser, Peter
Zhao, Lifu
Jo, Oak D.
Komeya, Mitsuru
Ogawa, Takehiko
Yanagawa, Norimoto
Effect of fluid shear stress on in vitro cultured ureteric bud cells
title Effect of fluid shear stress on in vitro cultured ureteric bud cells
title_full Effect of fluid shear stress on in vitro cultured ureteric bud cells
title_fullStr Effect of fluid shear stress on in vitro cultured ureteric bud cells
title_full_unstemmed Effect of fluid shear stress on in vitro cultured ureteric bud cells
title_short Effect of fluid shear stress on in vitro cultured ureteric bud cells
title_sort effect of fluid shear stress on in vitro cultured ureteric bud cells
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039298/
https://www.ncbi.nlm.nih.gov/pubmed/30034570
http://dx.doi.org/10.1063/1.5035328
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