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In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix

Our understanding of the spatiotemporal regulation of cardiogenesis is hindered by the difficulties in modeling this complex organ currently by in vitro models. Here we develop a method to generate heart organoids from mouse embryonic stem cell-derived embryoid bodies. Consecutive morphological chan...

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Autores principales: Lee, Jiyoung, Sutani, Akito, Kaneko, Rin, Takeuchi, Jun, Sasano, Tetsuo, Kohda, Takashi, Ihara, Kensuke, Takahashi, Kentaro, Yamazoe, Masahiro, Morio, Tomohiro, Furukawa, Tetsushi, Ishino, Fumitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471119/
https://www.ncbi.nlm.nih.gov/pubmed/32883967
http://dx.doi.org/10.1038/s41467-020-18031-5
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author Lee, Jiyoung
Sutani, Akito
Kaneko, Rin
Takeuchi, Jun
Sasano, Tetsuo
Kohda, Takashi
Ihara, Kensuke
Takahashi, Kentaro
Yamazoe, Masahiro
Morio, Tomohiro
Furukawa, Tetsushi
Ishino, Fumitoshi
author_facet Lee, Jiyoung
Sutani, Akito
Kaneko, Rin
Takeuchi, Jun
Sasano, Tetsuo
Kohda, Takashi
Ihara, Kensuke
Takahashi, Kentaro
Yamazoe, Masahiro
Morio, Tomohiro
Furukawa, Tetsushi
Ishino, Fumitoshi
author_sort Lee, Jiyoung
collection PubMed
description Our understanding of the spatiotemporal regulation of cardiogenesis is hindered by the difficulties in modeling this complex organ currently by in vitro models. Here we develop a method to generate heart organoids from mouse embryonic stem cell-derived embryoid bodies. Consecutive morphological changes proceed in a self-organizing manner in the presence of the laminin-entactin (LN/ET) complex and fibroblast growth factor 4 (FGF4), and the resulting in vitro heart organoid possesses atrium- and ventricle-like parts containing cardiac muscle, conducting tissues, smooth muscle and endothelial cells that exhibited myocardial contraction and action potentials. The heart organoids exhibit ultrastructural, histochemical and gene expression characteristics of considerable similarity to those of developmental hearts in vivo. Our results demonstrate that this method not only provides a biomimetic model of the developing heart-like structure with simplified differentiation protocol, but also represents a promising research tool with a broad range of applications, including drug testing.
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spelling pubmed-74711192020-09-16 In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix Lee, Jiyoung Sutani, Akito Kaneko, Rin Takeuchi, Jun Sasano, Tetsuo Kohda, Takashi Ihara, Kensuke Takahashi, Kentaro Yamazoe, Masahiro Morio, Tomohiro Furukawa, Tetsushi Ishino, Fumitoshi Nat Commun Article Our understanding of the spatiotemporal regulation of cardiogenesis is hindered by the difficulties in modeling this complex organ currently by in vitro models. Here we develop a method to generate heart organoids from mouse embryonic stem cell-derived embryoid bodies. Consecutive morphological changes proceed in a self-organizing manner in the presence of the laminin-entactin (LN/ET) complex and fibroblast growth factor 4 (FGF4), and the resulting in vitro heart organoid possesses atrium- and ventricle-like parts containing cardiac muscle, conducting tissues, smooth muscle and endothelial cells that exhibited myocardial contraction and action potentials. The heart organoids exhibit ultrastructural, histochemical and gene expression characteristics of considerable similarity to those of developmental hearts in vivo. Our results demonstrate that this method not only provides a biomimetic model of the developing heart-like structure with simplified differentiation protocol, but also represents a promising research tool with a broad range of applications, including drug testing. Nature Publishing Group UK 2020-09-03 /pmc/articles/PMC7471119/ /pubmed/32883967 http://dx.doi.org/10.1038/s41467-020-18031-5 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Jiyoung
Sutani, Akito
Kaneko, Rin
Takeuchi, Jun
Sasano, Tetsuo
Kohda, Takashi
Ihara, Kensuke
Takahashi, Kentaro
Yamazoe, Masahiro
Morio, Tomohiro
Furukawa, Tetsushi
Ishino, Fumitoshi
In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title_full In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title_fullStr In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title_full_unstemmed In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title_short In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix
title_sort in vitro generation of functional murine heart organoids via fgf4 and extracellular matrix
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471119/
https://www.ncbi.nlm.nih.gov/pubmed/32883967
http://dx.doi.org/10.1038/s41467-020-18031-5
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