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Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture

Cultured cell models are an essential complement to dissecting kidney proximal tubule (PT) function in health and disease but do not fully recapitulate key features of this nephron segment. We recently determined that culture of opossum kidney (OK) cells under continuous orbital shear stress (OSS) s...

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Autores principales: Park, Hyun Jung, Fan, Zhenjiang, Bai, Yulong, Ren, Qidong, Rbaibi, Youssef, Long, Kimberly R., Gliozzi, Megan L., Rittenhouse, Natalie, Locker, Joseph D., Poholek, Amanda C., Weisz, Ora A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662153/
https://www.ncbi.nlm.nih.gov/pubmed/33192601
http://dx.doi.org/10.3389/fphys.2020.587358
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author Park, Hyun Jung
Fan, Zhenjiang
Bai, Yulong
Ren, Qidong
Rbaibi, Youssef
Long, Kimberly R.
Gliozzi, Megan L.
Rittenhouse, Natalie
Locker, Joseph D.
Poholek, Amanda C.
Weisz, Ora A.
author_facet Park, Hyun Jung
Fan, Zhenjiang
Bai, Yulong
Ren, Qidong
Rbaibi, Youssef
Long, Kimberly R.
Gliozzi, Megan L.
Rittenhouse, Natalie
Locker, Joseph D.
Poholek, Amanda C.
Weisz, Ora A.
author_sort Park, Hyun Jung
collection PubMed
description Cultured cell models are an essential complement to dissecting kidney proximal tubule (PT) function in health and disease but do not fully recapitulate key features of this nephron segment. We recently determined that culture of opossum kidney (OK) cells under continuous orbital shear stress (OSS) significantly augments their morphological and functional resemblance to PTs in vivo. Here we used RNASeq to identify temporal transcriptional changes upon cell culture under static or shear stress conditions. Comparison of gene expression in cells cultured under static or OSS conditions with a database of rat nephron segment gene expression confirms that OK cells cultured under OSS are more similar to the PT in vivo compared with cells maintained under static conditions. Both improved oxygenation and mechanosensitive stimuli contribute to the enhanced differentiation in these cells, and we identified temporal changes in gene expression of known mechanosensitive targets. We observed changes in mRNA and protein levels of membrane trafficking components that may contribute to the enhanced endocytic capacity of cells cultured under OSS. Our data reveal pathways that may be critical for PT differentiation in vivo and validate the utility of this improved cell culture model as a tool to study PT function.
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spelling pubmed-76621532020-11-13 Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture Park, Hyun Jung Fan, Zhenjiang Bai, Yulong Ren, Qidong Rbaibi, Youssef Long, Kimberly R. Gliozzi, Megan L. Rittenhouse, Natalie Locker, Joseph D. Poholek, Amanda C. Weisz, Ora A. Front Physiol Physiology Cultured cell models are an essential complement to dissecting kidney proximal tubule (PT) function in health and disease but do not fully recapitulate key features of this nephron segment. We recently determined that culture of opossum kidney (OK) cells under continuous orbital shear stress (OSS) significantly augments their morphological and functional resemblance to PTs in vivo. Here we used RNASeq to identify temporal transcriptional changes upon cell culture under static or shear stress conditions. Comparison of gene expression in cells cultured under static or OSS conditions with a database of rat nephron segment gene expression confirms that OK cells cultured under OSS are more similar to the PT in vivo compared with cells maintained under static conditions. Both improved oxygenation and mechanosensitive stimuli contribute to the enhanced differentiation in these cells, and we identified temporal changes in gene expression of known mechanosensitive targets. We observed changes in mRNA and protein levels of membrane trafficking components that may contribute to the enhanced endocytic capacity of cells cultured under OSS. Our data reveal pathways that may be critical for PT differentiation in vivo and validate the utility of this improved cell culture model as a tool to study PT function. Frontiers Media S.A. 2020-10-30 /pmc/articles/PMC7662153/ /pubmed/33192601 http://dx.doi.org/10.3389/fphys.2020.587358 Text en Copyright © 2020 Park, Fan, Bai, Ren, Rbaibi, Long, Gliozzi, Rittenhouse, Locker, Poholek and Weisz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Park, Hyun Jung
Fan, Zhenjiang
Bai, Yulong
Ren, Qidong
Rbaibi, Youssef
Long, Kimberly R.
Gliozzi, Megan L.
Rittenhouse, Natalie
Locker, Joseph D.
Poholek, Amanda C.
Weisz, Ora A.
Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title_full Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title_fullStr Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title_full_unstemmed Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title_short Transcriptional Programs Driving Shear Stress-Induced Differentiation of Kidney Proximal Tubule Cells in Culture
title_sort transcriptional programs driving shear stress-induced differentiation of kidney proximal tubule cells in culture
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662153/
https://www.ncbi.nlm.nih.gov/pubmed/33192601
http://dx.doi.org/10.3389/fphys.2020.587358
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