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Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions

Although critical for studies of gut motility and intestinal regeneration, the in vitro culture of intestinal muscularis with peristaltic function remains a significant challenge. Periodic contractions of intestinal muscularis result from the coordinated activity of smooth muscle cells (SMC), the en...

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Autores principales: Wang, Qianqian, Wang, Ke, Solorzano-Vargas, R. Sergio, Lin, Po-Yu, Walthers, Christopher M., Thomas, Anne-Laure, Martín, Martín G., Dunn, James C. Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931477/
https://www.ncbi.nlm.nih.gov/pubmed/29718926
http://dx.doi.org/10.1371/journal.pone.0195315
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author Wang, Qianqian
Wang, Ke
Solorzano-Vargas, R. Sergio
Lin, Po-Yu
Walthers, Christopher M.
Thomas, Anne-Laure
Martín, Martín G.
Dunn, James C. Y.
author_facet Wang, Qianqian
Wang, Ke
Solorzano-Vargas, R. Sergio
Lin, Po-Yu
Walthers, Christopher M.
Thomas, Anne-Laure
Martín, Martín G.
Dunn, James C. Y.
author_sort Wang, Qianqian
collection PubMed
description Although critical for studies of gut motility and intestinal regeneration, the in vitro culture of intestinal muscularis with peristaltic function remains a significant challenge. Periodic contractions of intestinal muscularis result from the coordinated activity of smooth muscle cells (SMC), the enteric nervous system (ENS), and interstitial cells of Cajal (ICC). Reproducing this activity requires the preservation of all these cells in one system. Here we report the first serum-free culture methodology that consistently maintains spontaneous and periodic contractions of murine and human intestinal muscularis cells for months. In this system, SMC expressed the mature marker myosin heavy chain, and multipolar/dipolar ICC, uniaxonal/multipolar neurons and glial cells were present. Furthermore, drugs affecting neural signals, ICC or SMC altered the contractions. Combining this method with scaffolds, contracting cell sheets were formed with organized architecture. With the addition of intestinal epithelial cells, this platform enabled up to 11 types of cells from mucosa, muscularis and serosa to coexist and epithelial cells were stretched by the contracting muscularis cells. The method constitutes a powerful tool for mechanistic studies of gut motility disorders and the functional regeneration of the engineered intestine.
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spelling pubmed-59314772018-05-11 Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions Wang, Qianqian Wang, Ke Solorzano-Vargas, R. Sergio Lin, Po-Yu Walthers, Christopher M. Thomas, Anne-Laure Martín, Martín G. Dunn, James C. Y. PLoS One Research Article Although critical for studies of gut motility and intestinal regeneration, the in vitro culture of intestinal muscularis with peristaltic function remains a significant challenge. Periodic contractions of intestinal muscularis result from the coordinated activity of smooth muscle cells (SMC), the enteric nervous system (ENS), and interstitial cells of Cajal (ICC). Reproducing this activity requires the preservation of all these cells in one system. Here we report the first serum-free culture methodology that consistently maintains spontaneous and periodic contractions of murine and human intestinal muscularis cells for months. In this system, SMC expressed the mature marker myosin heavy chain, and multipolar/dipolar ICC, uniaxonal/multipolar neurons and glial cells were present. Furthermore, drugs affecting neural signals, ICC or SMC altered the contractions. Combining this method with scaffolds, contracting cell sheets were formed with organized architecture. With the addition of intestinal epithelial cells, this platform enabled up to 11 types of cells from mucosa, muscularis and serosa to coexist and epithelial cells were stretched by the contracting muscularis cells. The method constitutes a powerful tool for mechanistic studies of gut motility disorders and the functional regeneration of the engineered intestine. Public Library of Science 2018-05-02 /pmc/articles/PMC5931477/ /pubmed/29718926 http://dx.doi.org/10.1371/journal.pone.0195315 Text en © 2018 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Qianqian
Wang, Ke
Solorzano-Vargas, R. Sergio
Lin, Po-Yu
Walthers, Christopher M.
Thomas, Anne-Laure
Martín, Martín G.
Dunn, James C. Y.
Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title_full Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title_fullStr Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title_full_unstemmed Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title_short Bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
title_sort bioengineered intestinal muscularis complexes with long-term spontaneous and periodic contractions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931477/
https://www.ncbi.nlm.nih.gov/pubmed/29718926
http://dx.doi.org/10.1371/journal.pone.0195315
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