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Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery
The lack of engineering systems able to faithfully reproduce complex kidney structures in vitro has made it difficult to efficiently model kidney diseases and development. Using polydimethylsiloxane (PDMS) scaffolds and a kidney-derived cell line we developed a system to rapidly engineer custom-made...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085557/ https://www.ncbi.nlm.nih.gov/pubmed/30049385 http://dx.doi.org/10.1016/j.ebiom.2018.06.005 |
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author | Benedetti, Valentina Brizi, Valerio Guida, Patrizia Tomasoni, Susanna Ciampi, Osele Angeli, Elena Valbusa, Ugo Benigni, Ariela Remuzzi, Giuseppe Xinaris, Christodoulos |
author_facet | Benedetti, Valentina Brizi, Valerio Guida, Patrizia Tomasoni, Susanna Ciampi, Osele Angeli, Elena Valbusa, Ugo Benigni, Ariela Remuzzi, Giuseppe Xinaris, Christodoulos |
author_sort | Benedetti, Valentina |
collection | PubMed |
description | The lack of engineering systems able to faithfully reproduce complex kidney structures in vitro has made it difficult to efficiently model kidney diseases and development. Using polydimethylsiloxane (PDMS) scaffolds and a kidney-derived cell line we developed a system to rapidly engineer custom-made 3D tubules with typical renal epithelial properties. This system was successfully employed to engineer patient-specific tubules, to model polycystic kidney disease (PKD) and test drug efficacy, and to identify a potential new pharmacological treatment. By optimizing our system we constructed functional ureteric bud (UB)-like tubules from human induced pluripotent stem cells (iPSCs), and identified a combination of growth factors that induces budding morphogenesis like embryonic kidneys do. Finally, we applied this assay to investigate budding defects in UB-like tubules derived from a patient with a PAX2 mutation. Our system enables the modeling of human kidney disease and development, drug testing and discovery, and lays the groundwork for engineering anatomically correct kidney tissues in vitro and developing personalized medicine applications. |
format | Online Article Text |
id | pubmed-6085557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60855572018-08-13 Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery Benedetti, Valentina Brizi, Valerio Guida, Patrizia Tomasoni, Susanna Ciampi, Osele Angeli, Elena Valbusa, Ugo Benigni, Ariela Remuzzi, Giuseppe Xinaris, Christodoulos EBioMedicine Research Paper The lack of engineering systems able to faithfully reproduce complex kidney structures in vitro has made it difficult to efficiently model kidney diseases and development. Using polydimethylsiloxane (PDMS) scaffolds and a kidney-derived cell line we developed a system to rapidly engineer custom-made 3D tubules with typical renal epithelial properties. This system was successfully employed to engineer patient-specific tubules, to model polycystic kidney disease (PKD) and test drug efficacy, and to identify a potential new pharmacological treatment. By optimizing our system we constructed functional ureteric bud (UB)-like tubules from human induced pluripotent stem cells (iPSCs), and identified a combination of growth factors that induces budding morphogenesis like embryonic kidneys do. Finally, we applied this assay to investigate budding defects in UB-like tubules derived from a patient with a PAX2 mutation. Our system enables the modeling of human kidney disease and development, drug testing and discovery, and lays the groundwork for engineering anatomically correct kidney tissues in vitro and developing personalized medicine applications. Elsevier 2018-07-03 /pmc/articles/PMC6085557/ /pubmed/30049385 http://dx.doi.org/10.1016/j.ebiom.2018.06.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Benedetti, Valentina Brizi, Valerio Guida, Patrizia Tomasoni, Susanna Ciampi, Osele Angeli, Elena Valbusa, Ugo Benigni, Ariela Remuzzi, Giuseppe Xinaris, Christodoulos Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title | Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title_full | Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title_fullStr | Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title_full_unstemmed | Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title_short | Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery |
title_sort | engineered kidney tubules for modeling patient-specific diseases and drug discovery |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085557/ https://www.ncbi.nlm.nih.gov/pubmed/30049385 http://dx.doi.org/10.1016/j.ebiom.2018.06.005 |
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