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Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy
Glomerular hypertension is an important factor exacerbating glomerular diseases to end-stage renal diseases because, ultimately, it results in glomerular sclerosis (especially in hypertensive and diabetic nephropathy). The precise mechanism of glomerular sclerosis caused by glomerular hypertension i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997336/ https://www.ncbi.nlm.nih.gov/pubmed/27558173 http://dx.doi.org/10.1038/srep31771 |
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author | Zhou, Mengying Zhang, Xulang Wen, Xinyu Wu, Taihua Wang, Weidong Yang, Mingzhou Wang, Jing Fang, Ming Lin, Bingcheng Lin, Hongli |
author_facet | Zhou, Mengying Zhang, Xulang Wen, Xinyu Wu, Taihua Wang, Weidong Yang, Mingzhou Wang, Jing Fang, Ming Lin, Bingcheng Lin, Hongli |
author_sort | Zhou, Mengying |
collection | PubMed |
description | Glomerular hypertension is an important factor exacerbating glomerular diseases to end-stage renal diseases because, ultimately, it results in glomerular sclerosis (especially in hypertensive and diabetic nephropathy). The precise mechanism of glomerular sclerosis caused by glomerular hypertension is unclear, due partly to the absence of suitable in vitro or in vivo models capable of mimicking and regulating the complex mechanical forces and/or organ-level disease processes. We developed a “glomerulus-on-a-chip” (GC) microfluidic device. This device reconstitutes the glomerulus with organ-level glomerular functions to create a disease model-on-a chip that mimics hypertensive nephropathy in humans. It comprises two channels lined by closely opposed layers of glomerular endothelial cells and podocytes that experience fluid flow of physiological conditions to mimic the glomerular microenvironment in vivo. Our results revealed that glomerular mechanical forces have a crucial role in cellular cytoskeletal rearrangement as well as the damage to cells and their junctions that leads to increased glomerular leakage observed in hypertensive nephropathy. Results also showed that the GC could readily and flexibly meet the demands of a renal-disease model. The GC could provide drug screening and toxicology testing, and create potential new personalized and accurate therapeutic platforms for glomerular disease. |
format | Online Article Text |
id | pubmed-4997336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49973362016-09-01 Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy Zhou, Mengying Zhang, Xulang Wen, Xinyu Wu, Taihua Wang, Weidong Yang, Mingzhou Wang, Jing Fang, Ming Lin, Bingcheng Lin, Hongli Sci Rep Article Glomerular hypertension is an important factor exacerbating glomerular diseases to end-stage renal diseases because, ultimately, it results in glomerular sclerosis (especially in hypertensive and diabetic nephropathy). The precise mechanism of glomerular sclerosis caused by glomerular hypertension is unclear, due partly to the absence of suitable in vitro or in vivo models capable of mimicking and regulating the complex mechanical forces and/or organ-level disease processes. We developed a “glomerulus-on-a-chip” (GC) microfluidic device. This device reconstitutes the glomerulus with organ-level glomerular functions to create a disease model-on-a chip that mimics hypertensive nephropathy in humans. It comprises two channels lined by closely opposed layers of glomerular endothelial cells and podocytes that experience fluid flow of physiological conditions to mimic the glomerular microenvironment in vivo. Our results revealed that glomerular mechanical forces have a crucial role in cellular cytoskeletal rearrangement as well as the damage to cells and their junctions that leads to increased glomerular leakage observed in hypertensive nephropathy. Results also showed that the GC could readily and flexibly meet the demands of a renal-disease model. The GC could provide drug screening and toxicology testing, and create potential new personalized and accurate therapeutic platforms for glomerular disease. Nature Publishing Group 2016-08-25 /pmc/articles/PMC4997336/ /pubmed/27558173 http://dx.doi.org/10.1038/srep31771 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhou, Mengying Zhang, Xulang Wen, Xinyu Wu, Taihua Wang, Weidong Yang, Mingzhou Wang, Jing Fang, Ming Lin, Bingcheng Lin, Hongli Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title | Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title_full | Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title_fullStr | Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title_full_unstemmed | Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title_short | Development of a Functional Glomerulus at the Organ Level on a Chip to Mimic Hypertensive Nephropathy |
title_sort | development of a functional glomerulus at the organ level on a chip to mimic hypertensive nephropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997336/ https://www.ncbi.nlm.nih.gov/pubmed/27558173 http://dx.doi.org/10.1038/srep31771 |
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