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Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation.
Directed differentiation of human pluripotent stem cells to kidney organoids brings the prospect of drug screening, disease modelling and the generation of tissue for renal replacement. Currently, these applications are hampered by organoid variability, nephron immaturity, low throughput and limited...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855371/ https://www.ncbi.nlm.nih.gov/pubmed/33230326 http://dx.doi.org/10.1038/s41563-020-00853-9 |
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author | Lawlor, Kynan T. Vanslambrouck, Jessica M. Higgins, J. William Chambon, Alison Bishard, Kristina Arndt, Derek Er, Pei Xuan Wilson, Sean B. Howden, Sara E. Tan, Ker Sin Li, Fanyi Hale, Lorna J. Shepherd, Benjamin Pentoney, Stephen Presnell, Sharon C. Chen, Alice E. Little, Melissa H. |
author_facet | Lawlor, Kynan T. Vanslambrouck, Jessica M. Higgins, J. William Chambon, Alison Bishard, Kristina Arndt, Derek Er, Pei Xuan Wilson, Sean B. Howden, Sara E. Tan, Ker Sin Li, Fanyi Hale, Lorna J. Shepherd, Benjamin Pentoney, Stephen Presnell, Sharon C. Chen, Alice E. Little, Melissa H. |
author_sort | Lawlor, Kynan T. |
collection | PubMed |
description | Directed differentiation of human pluripotent stem cells to kidney organoids brings the prospect of drug screening, disease modelling and the generation of tissue for renal replacement. Currently, these applications are hampered by organoid variability, nephron immaturity, low throughput and limited scale. Here we apply extrusion-based 3D cellular bioprinting to deliver rapid and high throughput generation of kidney organoids with highly reproducible cell number and viability. We demonstrate that manual organoid generation can be replaced by 6- or 96-well organoid bioprinting and evaluate relative toxicity of aminoglycosides as a proof of concept for drug testing. In addition, 3D bioprinting enabled precise manipulation of biophysical properties including organoid size, cell number and conformation, with modification of organoid conformation substantially increasing nephron yield per starting cell number. This facilitated the manufacture of uniformly patterned kidney tissue sheets with functional proximal tubular segments. Hence, automated extrusion-based bioprinting for kidney organoid production deliver improvements in throughput, quality control, scale and structure, facilitating in vitro and in vivo applications of stem cell-derived human kidney tissue. |
format | Online Article Text |
id | pubmed-7855371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-78553712021-05-23 Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. Lawlor, Kynan T. Vanslambrouck, Jessica M. Higgins, J. William Chambon, Alison Bishard, Kristina Arndt, Derek Er, Pei Xuan Wilson, Sean B. Howden, Sara E. Tan, Ker Sin Li, Fanyi Hale, Lorna J. Shepherd, Benjamin Pentoney, Stephen Presnell, Sharon C. Chen, Alice E. Little, Melissa H. Nat Mater Article Directed differentiation of human pluripotent stem cells to kidney organoids brings the prospect of drug screening, disease modelling and the generation of tissue for renal replacement. Currently, these applications are hampered by organoid variability, nephron immaturity, low throughput and limited scale. Here we apply extrusion-based 3D cellular bioprinting to deliver rapid and high throughput generation of kidney organoids with highly reproducible cell number and viability. We demonstrate that manual organoid generation can be replaced by 6- or 96-well organoid bioprinting and evaluate relative toxicity of aminoglycosides as a proof of concept for drug testing. In addition, 3D bioprinting enabled precise manipulation of biophysical properties including organoid size, cell number and conformation, with modification of organoid conformation substantially increasing nephron yield per starting cell number. This facilitated the manufacture of uniformly patterned kidney tissue sheets with functional proximal tubular segments. Hence, automated extrusion-based bioprinting for kidney organoid production deliver improvements in throughput, quality control, scale and structure, facilitating in vitro and in vivo applications of stem cell-derived human kidney tissue. 2020-11-23 2021-02 /pmc/articles/PMC7855371/ /pubmed/33230326 http://dx.doi.org/10.1038/s41563-020-00853-9 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lawlor, Kynan T. Vanslambrouck, Jessica M. Higgins, J. William Chambon, Alison Bishard, Kristina Arndt, Derek Er, Pei Xuan Wilson, Sean B. Howden, Sara E. Tan, Ker Sin Li, Fanyi Hale, Lorna J. Shepherd, Benjamin Pentoney, Stephen Presnell, Sharon C. Chen, Alice E. Little, Melissa H. Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title | Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title_full | Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title_fullStr | Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title_full_unstemmed | Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title_short | Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
title_sort | cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855371/ https://www.ncbi.nlm.nih.gov/pubmed/33230326 http://dx.doi.org/10.1038/s41563-020-00853-9 |
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