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Do not keep it simple: recent advances in the generation of complex organoids
3D cell culture models which closely resemble real human tissues are of high interest for disease modelling, drug screening as well as a deeper understanding of human developmental biology. Such structures are termed organoids. Within the last years, several human organoid models were described. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Vienna
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577912/ https://www.ncbi.nlm.nih.gov/pubmed/32385575 http://dx.doi.org/10.1007/s00702-020-02198-8 |
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author | Wörsdörfer, Philipp I, Takashi Asahina, Izumi Sumita, Yoshinori Ergün, Süleyman |
author_facet | Wörsdörfer, Philipp I, Takashi Asahina, Izumi Sumita, Yoshinori Ergün, Süleyman |
author_sort | Wörsdörfer, Philipp |
collection | PubMed |
description | 3D cell culture models which closely resemble real human tissues are of high interest for disease modelling, drug screening as well as a deeper understanding of human developmental biology. Such structures are termed organoids. Within the last years, several human organoid models were described. These are usually stem cell derived, arise by self-organization, mimic mechanisms of normal tissue development, show typical organ morphogenesis and recapitulate at least some organ specific functions. Many tissues have been reproduced in vitro such as gut, liver, lung, kidney and brain. The resulting entities can be either derived from an adult stem cell population, or generated from pluripotent stem cells using a specific differentiation protocol. However, many organoid models only recapitulate the organs parenchyma but are devoid of stromal components such as blood vessels, connective tissue and inflammatory cells. Recent studies show that the incorporation of endothelial and mesenchymal cells into organoids improved their maturation and might be required to create fully functional micro-tissues, which will allow deeper insights into human embryogenesis as well as disease development and progression. In this review article, we will summarize and discuss recent works trying to incorporate stromal components into organoids, with a special focus on neural organoid models. |
format | Online Article Text |
id | pubmed-7577912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-75779122020-10-27 Do not keep it simple: recent advances in the generation of complex organoids Wörsdörfer, Philipp I, Takashi Asahina, Izumi Sumita, Yoshinori Ergün, Süleyman J Neural Transm (Vienna) Neurology and Preclinical Neurological Studies - Review Article 3D cell culture models which closely resemble real human tissues are of high interest for disease modelling, drug screening as well as a deeper understanding of human developmental biology. Such structures are termed organoids. Within the last years, several human organoid models were described. These are usually stem cell derived, arise by self-organization, mimic mechanisms of normal tissue development, show typical organ morphogenesis and recapitulate at least some organ specific functions. Many tissues have been reproduced in vitro such as gut, liver, lung, kidney and brain. The resulting entities can be either derived from an adult stem cell population, or generated from pluripotent stem cells using a specific differentiation protocol. However, many organoid models only recapitulate the organs parenchyma but are devoid of stromal components such as blood vessels, connective tissue and inflammatory cells. Recent studies show that the incorporation of endothelial and mesenchymal cells into organoids improved their maturation and might be required to create fully functional micro-tissues, which will allow deeper insights into human embryogenesis as well as disease development and progression. In this review article, we will summarize and discuss recent works trying to incorporate stromal components into organoids, with a special focus on neural organoid models. Springer Vienna 2020-05-08 2020 /pmc/articles/PMC7577912/ /pubmed/32385575 http://dx.doi.org/10.1007/s00702-020-02198-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Neurology and Preclinical Neurological Studies - Review Article Wörsdörfer, Philipp I, Takashi Asahina, Izumi Sumita, Yoshinori Ergün, Süleyman Do not keep it simple: recent advances in the generation of complex organoids |
title | Do not keep it simple: recent advances in the generation of complex organoids |
title_full | Do not keep it simple: recent advances in the generation of complex organoids |
title_fullStr | Do not keep it simple: recent advances in the generation of complex organoids |
title_full_unstemmed | Do not keep it simple: recent advances in the generation of complex organoids |
title_short | Do not keep it simple: recent advances in the generation of complex organoids |
title_sort | do not keep it simple: recent advances in the generation of complex organoids |
topic | Neurology and Preclinical Neurological Studies - Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577912/ https://www.ncbi.nlm.nih.gov/pubmed/32385575 http://dx.doi.org/10.1007/s00702-020-02198-8 |
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