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Gut-on-a-chip for exploring the transport mechanism of Hg(II)

Animal models and static cultures of intestinal epithelial cells are commonly used platforms for exploring mercury ion (Hg(II)) transport. However, they cannot reliably simulate the human intestinal microenvironment and monitor cellular physiology in situ; thus, the mechanism of Hg(II) transport in...

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Autores principales: Wang, Li, Han, Junlei, Su, Weiguang, Li, Anqing, Zhang, Wenxian, Li, Huimin, Hu, Huili, Song, Wei, Xu, Chonghai, Chen, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805456/
https://www.ncbi.nlm.nih.gov/pubmed/36597512
http://dx.doi.org/10.1038/s41378-022-00447-2
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author Wang, Li
Han, Junlei
Su, Weiguang
Li, Anqing
Zhang, Wenxian
Li, Huimin
Hu, Huili
Song, Wei
Xu, Chonghai
Chen, Jun
author_facet Wang, Li
Han, Junlei
Su, Weiguang
Li, Anqing
Zhang, Wenxian
Li, Huimin
Hu, Huili
Song, Wei
Xu, Chonghai
Chen, Jun
author_sort Wang, Li
collection PubMed
description Animal models and static cultures of intestinal epithelial cells are commonly used platforms for exploring mercury ion (Hg(II)) transport. However, they cannot reliably simulate the human intestinal microenvironment and monitor cellular physiology in situ; thus, the mechanism of Hg(II) transport in the human intestine is still unclear. Here, a gut-on-a-chip integrated with transepithelial electrical resistance (TEER) sensors and electrochemical sensors is proposed for dynamically simulating the formation of the physical intestinal barrier and monitoring the transport and absorption of Hg(II) in situ. The cellular microenvironment was recreated by applying fluid shear stress (0.02 dyne/cm(2)) and cyclic mechanical strain (1%, 0.15 Hz). Hg(II) absorption and physical damage to cells were simultaneously monitored by electrochemical and TEER sensors when intestinal epithelial cells were exposed to different concentrations of Hg(II) mixed in culture medium. Hg(II) absorption increased by 23.59% when tensile strain increased from 1% to 5%, and the corresponding expression of Piezo1 and DMT1 on the cell surface was upregulated. [Image: see text]
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spelling pubmed-98054562023-01-02 Gut-on-a-chip for exploring the transport mechanism of Hg(II) Wang, Li Han, Junlei Su, Weiguang Li, Anqing Zhang, Wenxian Li, Huimin Hu, Huili Song, Wei Xu, Chonghai Chen, Jun Microsyst Nanoeng Article Animal models and static cultures of intestinal epithelial cells are commonly used platforms for exploring mercury ion (Hg(II)) transport. However, they cannot reliably simulate the human intestinal microenvironment and monitor cellular physiology in situ; thus, the mechanism of Hg(II) transport in the human intestine is still unclear. Here, a gut-on-a-chip integrated with transepithelial electrical resistance (TEER) sensors and electrochemical sensors is proposed for dynamically simulating the formation of the physical intestinal barrier and monitoring the transport and absorption of Hg(II) in situ. The cellular microenvironment was recreated by applying fluid shear stress (0.02 dyne/cm(2)) and cyclic mechanical strain (1%, 0.15 Hz). Hg(II) absorption and physical damage to cells were simultaneously monitored by electrochemical and TEER sensors when intestinal epithelial cells were exposed to different concentrations of Hg(II) mixed in culture medium. Hg(II) absorption increased by 23.59% when tensile strain increased from 1% to 5%, and the corresponding expression of Piezo1 and DMT1 on the cell surface was upregulated. [Image: see text] Nature Publishing Group UK 2023-01-01 /pmc/articles/PMC9805456/ /pubmed/36597512 http://dx.doi.org/10.1038/s41378-022-00447-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Li
Han, Junlei
Su, Weiguang
Li, Anqing
Zhang, Wenxian
Li, Huimin
Hu, Huili
Song, Wei
Xu, Chonghai
Chen, Jun
Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title_full Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title_fullStr Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title_full_unstemmed Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title_short Gut-on-a-chip for exploring the transport mechanism of Hg(II)
title_sort gut-on-a-chip for exploring the transport mechanism of hg(ii)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805456/
https://www.ncbi.nlm.nih.gov/pubmed/36597512
http://dx.doi.org/10.1038/s41378-022-00447-2
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