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Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform

Many drugs have progressed through preclinical and clinical trials and have been available – for years in some cases – before being recalled by the FDA for unanticipated toxicity in humans. One reason for such poor translation from drug candidate to successful use is a lack of model systems that acc...

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Autores principales: Skardal, Aleksander, Murphy, Sean V., Devarasetty, Mahesh, Mead, Ivy, Kang, Hyun-Wook, Seol, Young-Joon, Shrike Zhang, Yu, Shin, Su-Ryon, Zhao, Liang, Aleman, Julio, Hall, Adam R., Shupe, Thomas D., Kleensang, Andre, Dokmeci, Mehmet R., Jin Lee, Sang, Jackson, John D., Yoo, James J., Hartung, Thomas, Khademhosseini, Ali, Soker, Shay, Bishop, Colin E., Atala, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562747/
https://www.ncbi.nlm.nih.gov/pubmed/28821762
http://dx.doi.org/10.1038/s41598-017-08879-x
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author Skardal, Aleksander
Murphy, Sean V.
Devarasetty, Mahesh
Mead, Ivy
Kang, Hyun-Wook
Seol, Young-Joon
Shrike Zhang, Yu
Shin, Su-Ryon
Zhao, Liang
Aleman, Julio
Hall, Adam R.
Shupe, Thomas D.
Kleensang, Andre
Dokmeci, Mehmet R.
Jin Lee, Sang
Jackson, John D.
Yoo, James J.
Hartung, Thomas
Khademhosseini, Ali
Soker, Shay
Bishop, Colin E.
Atala, Anthony
author_facet Skardal, Aleksander
Murphy, Sean V.
Devarasetty, Mahesh
Mead, Ivy
Kang, Hyun-Wook
Seol, Young-Joon
Shrike Zhang, Yu
Shin, Su-Ryon
Zhao, Liang
Aleman, Julio
Hall, Adam R.
Shupe, Thomas D.
Kleensang, Andre
Dokmeci, Mehmet R.
Jin Lee, Sang
Jackson, John D.
Yoo, James J.
Hartung, Thomas
Khademhosseini, Ali
Soker, Shay
Bishop, Colin E.
Atala, Anthony
author_sort Skardal, Aleksander
collection PubMed
description Many drugs have progressed through preclinical and clinical trials and have been available – for years in some cases – before being recalled by the FDA for unanticipated toxicity in humans. One reason for such poor translation from drug candidate to successful use is a lack of model systems that accurately recapitulate normal tissue function of human organs and their response to drug compounds. Moreover, tissues in the body do not exist in isolation, but reside in a highly integrated and dynamically interactive environment, in which actions in one tissue can affect other downstream tissues. Few engineered model systems, including the growing variety of organoid and organ-on-a-chip platforms, have so far reflected the interactive nature of the human body. To address this challenge, we have developed an assortment of bioengineered tissue organoids and tissue constructs that are integrated in a closed circulatory perfusion system, facilitating inter-organ responses. We describe a three-tissue organ-on-a-chip system, comprised of liver, heart, and lung, and highlight examples of inter-organ responses to drug administration. We observe drug responses that depend on inter-tissue interaction, illustrating the value of multiple tissue integration for in vitro study of both the efficacy of and side effects associated with candidate drugs.
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spelling pubmed-55627472017-08-21 Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform Skardal, Aleksander Murphy, Sean V. Devarasetty, Mahesh Mead, Ivy Kang, Hyun-Wook Seol, Young-Joon Shrike Zhang, Yu Shin, Su-Ryon Zhao, Liang Aleman, Julio Hall, Adam R. Shupe, Thomas D. Kleensang, Andre Dokmeci, Mehmet R. Jin Lee, Sang Jackson, John D. Yoo, James J. Hartung, Thomas Khademhosseini, Ali Soker, Shay Bishop, Colin E. Atala, Anthony Sci Rep Article Many drugs have progressed through preclinical and clinical trials and have been available – for years in some cases – before being recalled by the FDA for unanticipated toxicity in humans. One reason for such poor translation from drug candidate to successful use is a lack of model systems that accurately recapitulate normal tissue function of human organs and their response to drug compounds. Moreover, tissues in the body do not exist in isolation, but reside in a highly integrated and dynamically interactive environment, in which actions in one tissue can affect other downstream tissues. Few engineered model systems, including the growing variety of organoid and organ-on-a-chip platforms, have so far reflected the interactive nature of the human body. To address this challenge, we have developed an assortment of bioengineered tissue organoids and tissue constructs that are integrated in a closed circulatory perfusion system, facilitating inter-organ responses. We describe a three-tissue organ-on-a-chip system, comprised of liver, heart, and lung, and highlight examples of inter-organ responses to drug administration. We observe drug responses that depend on inter-tissue interaction, illustrating the value of multiple tissue integration for in vitro study of both the efficacy of and side effects associated with candidate drugs. Nature Publishing Group UK 2017-08-18 /pmc/articles/PMC5562747/ /pubmed/28821762 http://dx.doi.org/10.1038/s41598-017-08879-x Text en © The Author(s) 2017 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
Skardal, Aleksander
Murphy, Sean V.
Devarasetty, Mahesh
Mead, Ivy
Kang, Hyun-Wook
Seol, Young-Joon
Shrike Zhang, Yu
Shin, Su-Ryon
Zhao, Liang
Aleman, Julio
Hall, Adam R.
Shupe, Thomas D.
Kleensang, Andre
Dokmeci, Mehmet R.
Jin Lee, Sang
Jackson, John D.
Yoo, James J.
Hartung, Thomas
Khademhosseini, Ali
Soker, Shay
Bishop, Colin E.
Atala, Anthony
Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title_full Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title_fullStr Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title_full_unstemmed Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title_short Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
title_sort multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562747/
https://www.ncbi.nlm.nih.gov/pubmed/28821762
http://dx.doi.org/10.1038/s41598-017-08879-x
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