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Tissue engineering to better understand senescence: Organotypics come of age

The recent advent of ‘organs in a dish’ has revolutionised the research landscape. These 3D culture systems have paved the way for translational, post genomics research by enabling scientists to model diseases in the laboratory, grow patient-derived organoids, and unite this technology with other cu...

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Detalles Bibliográficos
Autores principales: Milligan, Deborah A., Tyler, Eleanor J., Bishop, Cleo L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ireland 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493709/
https://www.ncbi.nlm.nih.gov/pubmed/32461142
http://dx.doi.org/10.1016/j.mad.2020.111261
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author Milligan, Deborah A.
Tyler, Eleanor J.
Bishop, Cleo L.
author_facet Milligan, Deborah A.
Tyler, Eleanor J.
Bishop, Cleo L.
author_sort Milligan, Deborah A.
collection PubMed
description The recent advent of ‘organs in a dish’ has revolutionised the research landscape. These 3D culture systems have paved the way for translational, post genomics research by enabling scientists to model diseases in the laboratory, grow patient-derived organoids, and unite this technology with other cutting-edge methodologies such as drug discovery. Fields such as dermatology and neuroscience have revolutionised the development of robust 3D models, which faithfully recapitulate native physiology in vivo to provide important functional and mechanistic insights. These models have underpinned a rapid growth in the number of organs and myriad of human diseases that can be modelled in 3D, which currently includes breast, cerebral cortex, heart, intestine, kidney, liver, lung, neural tube, pancreas, prostate, skin and stomach, as well as patient derived tumours. However, so far, they have not yet been employed extensively in the study of fundamental cellular programmes such as senescence. Thus, tissue engineering and 3D culture offer an exciting opportunity to further understand the bright and dark sides of senescence in a more complex and physiologically relevant environment. Below, we will discuss previous approaches to investigating senescence and ageing using organotypic models, and some potential opportunities for future research.
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spelling pubmed-74937092020-09-24 Tissue engineering to better understand senescence: Organotypics come of age Milligan, Deborah A. Tyler, Eleanor J. Bishop, Cleo L. Mech Ageing Dev Original Article The recent advent of ‘organs in a dish’ has revolutionised the research landscape. These 3D culture systems have paved the way for translational, post genomics research by enabling scientists to model diseases in the laboratory, grow patient-derived organoids, and unite this technology with other cutting-edge methodologies such as drug discovery. Fields such as dermatology and neuroscience have revolutionised the development of robust 3D models, which faithfully recapitulate native physiology in vivo to provide important functional and mechanistic insights. These models have underpinned a rapid growth in the number of organs and myriad of human diseases that can be modelled in 3D, which currently includes breast, cerebral cortex, heart, intestine, kidney, liver, lung, neural tube, pancreas, prostate, skin and stomach, as well as patient derived tumours. However, so far, they have not yet been employed extensively in the study of fundamental cellular programmes such as senescence. Thus, tissue engineering and 3D culture offer an exciting opportunity to further understand the bright and dark sides of senescence in a more complex and physiologically relevant environment. Below, we will discuss previous approaches to investigating senescence and ageing using organotypic models, and some potential opportunities for future research. Elsevier Science Ireland 2020-09 /pmc/articles/PMC7493709/ /pubmed/32461142 http://dx.doi.org/10.1016/j.mad.2020.111261 Text en Crown Copyright © 2020 Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Milligan, Deborah A.
Tyler, Eleanor J.
Bishop, Cleo L.
Tissue engineering to better understand senescence: Organotypics come of age
title Tissue engineering to better understand senescence: Organotypics come of age
title_full Tissue engineering to better understand senescence: Organotypics come of age
title_fullStr Tissue engineering to better understand senescence: Organotypics come of age
title_full_unstemmed Tissue engineering to better understand senescence: Organotypics come of age
title_short Tissue engineering to better understand senescence: Organotypics come of age
title_sort tissue engineering to better understand senescence: organotypics come of age
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493709/
https://www.ncbi.nlm.nih.gov/pubmed/32461142
http://dx.doi.org/10.1016/j.mad.2020.111261
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