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Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques

The number of patients with end-stage renal disease is continuously increasing worldwide. The only therapies for these patients are dialysis and organ transplantation, but the latter is limited due to the insufficient number of donor kidneys available. Research in kidney disease and alternative ther...

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Autores principales: Fransen, Maaike F.J., Addario, Gabriele, Bouten, Carlijn V.C., Halary, Franck, Moroni, Lorenzo, Mota, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365327/
https://www.ncbi.nlm.nih.gov/pubmed/34096573
http://dx.doi.org/10.1042/EBC20200158
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author Fransen, Maaike F.J.
Addario, Gabriele
Bouten, Carlijn V.C.
Halary, Franck
Moroni, Lorenzo
Mota, Carlos
author_facet Fransen, Maaike F.J.
Addario, Gabriele
Bouten, Carlijn V.C.
Halary, Franck
Moroni, Lorenzo
Mota, Carlos
author_sort Fransen, Maaike F.J.
collection PubMed
description The number of patients with end-stage renal disease is continuously increasing worldwide. The only therapies for these patients are dialysis and organ transplantation, but the latter is limited due to the insufficient number of donor kidneys available. Research in kidney disease and alternative therapies are therefore of outmost importance. In vitro models that mimic human kidney functions are essential to provide better insights in disease and ultimately novel therapies. Bioprinting techniques have been increasingly used to create models with some degree of function, but their true potential is yet to be achieved. Bioprinted renal tissues and kidney-like constructs presents challenges, for example, choosing suitable renal cells and biomaterials for the formulation of bioinks. In addition, the fabrication of complex renal biological structures is still a major bottleneck. Advances in pluripotent stem cell-derived renal progenitors has contributed to in vivo-like rudiment structures with multiple renal cells, and these started to make a great impact on the achieved models. Natural- or synthetic-based biomaterial inks, such as kidney-derived extracellular matrix and gelatin-fibrin hydrogels, which show the potential to partially replicate in vivo-like microenvironments, have been largely investigated for bioprinting. As the field progresses, technological, biological and biomaterial developments will be required to yield fully functional in vitro tissues that can contribute to a better understanding of renal disease, to improve predictability in vitro of novel therapeutics, and to facilitate the development of alternative regenerative or replacement treatments. In this review, we resume the main advances on kidney in vitro models reported so far.
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spelling pubmed-83653272021-08-25 Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques Fransen, Maaike F.J. Addario, Gabriele Bouten, Carlijn V.C. Halary, Franck Moroni, Lorenzo Mota, Carlos Essays Biochem Stem Cells The number of patients with end-stage renal disease is continuously increasing worldwide. The only therapies for these patients are dialysis and organ transplantation, but the latter is limited due to the insufficient number of donor kidneys available. Research in kidney disease and alternative therapies are therefore of outmost importance. In vitro models that mimic human kidney functions are essential to provide better insights in disease and ultimately novel therapies. Bioprinting techniques have been increasingly used to create models with some degree of function, but their true potential is yet to be achieved. Bioprinted renal tissues and kidney-like constructs presents challenges, for example, choosing suitable renal cells and biomaterials for the formulation of bioinks. In addition, the fabrication of complex renal biological structures is still a major bottleneck. Advances in pluripotent stem cell-derived renal progenitors has contributed to in vivo-like rudiment structures with multiple renal cells, and these started to make a great impact on the achieved models. Natural- or synthetic-based biomaterial inks, such as kidney-derived extracellular matrix and gelatin-fibrin hydrogels, which show the potential to partially replicate in vivo-like microenvironments, have been largely investigated for bioprinting. As the field progresses, technological, biological and biomaterial developments will be required to yield fully functional in vitro tissues that can contribute to a better understanding of renal disease, to improve predictability in vitro of novel therapeutics, and to facilitate the development of alternative regenerative or replacement treatments. In this review, we resume the main advances on kidney in vitro models reported so far. Portland Press Ltd. 2021-08 2021-08-06 /pmc/articles/PMC8365327/ /pubmed/34096573 http://dx.doi.org/10.1042/EBC20200158 Text en © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Stem Cells
Fransen, Maaike F.J.
Addario, Gabriele
Bouten, Carlijn V.C.
Halary, Franck
Moroni, Lorenzo
Mota, Carlos
Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title_full Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title_fullStr Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title_full_unstemmed Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title_short Bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
title_sort bioprinting of kidney in vitro models: cells, biomaterials, and manufacturing techniques
topic Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365327/
https://www.ncbi.nlm.nih.gov/pubmed/34096573
http://dx.doi.org/10.1042/EBC20200158
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