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Pressure and stretch differentially affect proliferation of renal proximal tubular cells
Renal obstruction is frequently found in adults and children. Mechanical stimuli, including pressure and stretch in the obstructed kidney, contribute to damage; animal models of obstruction are characterized by increased cellular proliferation. We were interested in the direct effects of pressure an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599855/ https://www.ncbi.nlm.nih.gov/pubmed/28904080 http://dx.doi.org/10.14814/phy2.13346 |
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author | Felsen, Diane Diaz, Bianca J. Chen, Jie Gonzalez, Juana Kristensen, Marie Louise V. Bohn, Anja B. Roth, Brendan T. Poppas, Dix P. Nørregaard, Rikke |
author_facet | Felsen, Diane Diaz, Bianca J. Chen, Jie Gonzalez, Juana Kristensen, Marie Louise V. Bohn, Anja B. Roth, Brendan T. Poppas, Dix P. Nørregaard, Rikke |
author_sort | Felsen, Diane |
collection | PubMed |
description | Renal obstruction is frequently found in adults and children. Mechanical stimuli, including pressure and stretch in the obstructed kidney, contribute to damage; animal models of obstruction are characterized by increased cellular proliferation. We were interested in the direct effects of pressure and stretch on renal tubular cell proliferation. Human HKC‐8 or rat NRK‐52E proximal tubule cells were subjected to either pressure [0, 60 or 90 mmHg] or static stretch [0 or 20%] for 24 or 48 h. Cell proliferation was measured by cell counting, cell cycle analyzed by flow cytometry, and PCNA and Skp2 expression were determined by qPCR or western blot. Blood gases were determined in an iSTAT system. Proliferation was also assessed in vivo after 24 h of ureteral obstruction. There was a significant increase in HKC‐8 cell number after 48 h of exposure to either 60 or 90 mmHg pressure. Western blot and qPCR confirmed increased expression of PCNA and Skp2 in pressurized cells. Cell cycle measurements demonstrated an increase in HKC‐8 in S phase. Mechanical stretching increased PCNA protein expression in HKC‐8 cells after 48 h while no effect was observed on Skp2 and cell cycle measurements. Increased PCNA expression was found at 24 h after ureteral obstruction. We demonstrate direct transduction of pressure into a proliferative response in HKC‐8 and NRK‐52E cells, measured by cell number, PCNA and Skp2 expression and increase in cells in S phase, whereas stretch had a less robust effect on proliferation. |
format | Online Article Text |
id | pubmed-5599855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55998552017-09-19 Pressure and stretch differentially affect proliferation of renal proximal tubular cells Felsen, Diane Diaz, Bianca J. Chen, Jie Gonzalez, Juana Kristensen, Marie Louise V. Bohn, Anja B. Roth, Brendan T. Poppas, Dix P. Nørregaard, Rikke Physiol Rep Original Research Renal obstruction is frequently found in adults and children. Mechanical stimuli, including pressure and stretch in the obstructed kidney, contribute to damage; animal models of obstruction are characterized by increased cellular proliferation. We were interested in the direct effects of pressure and stretch on renal tubular cell proliferation. Human HKC‐8 or rat NRK‐52E proximal tubule cells were subjected to either pressure [0, 60 or 90 mmHg] or static stretch [0 or 20%] for 24 or 48 h. Cell proliferation was measured by cell counting, cell cycle analyzed by flow cytometry, and PCNA and Skp2 expression were determined by qPCR or western blot. Blood gases were determined in an iSTAT system. Proliferation was also assessed in vivo after 24 h of ureteral obstruction. There was a significant increase in HKC‐8 cell number after 48 h of exposure to either 60 or 90 mmHg pressure. Western blot and qPCR confirmed increased expression of PCNA and Skp2 in pressurized cells. Cell cycle measurements demonstrated an increase in HKC‐8 in S phase. Mechanical stretching increased PCNA protein expression in HKC‐8 cells after 48 h while no effect was observed on Skp2 and cell cycle measurements. Increased PCNA expression was found at 24 h after ureteral obstruction. We demonstrate direct transduction of pressure into a proliferative response in HKC‐8 and NRK‐52E cells, measured by cell number, PCNA and Skp2 expression and increase in cells in S phase, whereas stretch had a less robust effect on proliferation. John Wiley and Sons Inc. 2017-09-14 /pmc/articles/PMC5599855/ /pubmed/28904080 http://dx.doi.org/10.14814/phy2.13346 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Felsen, Diane Diaz, Bianca J. Chen, Jie Gonzalez, Juana Kristensen, Marie Louise V. Bohn, Anja B. Roth, Brendan T. Poppas, Dix P. Nørregaard, Rikke Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title | Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title_full | Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title_fullStr | Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title_full_unstemmed | Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title_short | Pressure and stretch differentially affect proliferation of renal proximal tubular cells |
title_sort | pressure and stretch differentially affect proliferation of renal proximal tubular cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599855/ https://www.ncbi.nlm.nih.gov/pubmed/28904080 http://dx.doi.org/10.14814/phy2.13346 |
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