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Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models
Epithelial tissues are composed of layers of tightly connected cells shaped into complex three-dimensional (3D) structures such as cysts, tubules, or invaginations. These complex 3D structures are important for organ-specific functions and often create biochemical gradients that guide cell positioni...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305315/ https://www.ncbi.nlm.nih.gov/pubmed/30619844 http://dx.doi.org/10.3389/fbioe.2018.00197 |
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author | Torras, Núria García-Díaz, María Fernández-Majada, Vanesa Martínez, Elena |
author_facet | Torras, Núria García-Díaz, María Fernández-Majada, Vanesa Martínez, Elena |
author_sort | Torras, Núria |
collection | PubMed |
description | Epithelial tissues are composed of layers of tightly connected cells shaped into complex three-dimensional (3D) structures such as cysts, tubules, or invaginations. These complex 3D structures are important for organ-specific functions and often create biochemical gradients that guide cell positioning and compartmentalization within the organ. One of the main functions of epithelia is to act as physical barriers that protect the underlying tissues from external insults. In vitro, epithelial barriers are usually mimicked by oversimplified models based on cell lines grown as monolayers on flat surfaces. While useful to answer certain questions, these models cannot fully capture the in vivo organ physiology and often yield poor predictions. In order to progress further in basic and translational research, disease modeling, drug discovery, and regenerative medicine, it is essential to advance the development of new in vitro predictive models of epithelial tissues that are capable of representing the in vivo-like structures and organ functionality more accurately. Here, we review current strategies for obtaining biomimetic systems in the form of advanced in vitro models that allow for more reliable and safer preclinical tests. The current state of the art and potential applications of self-organized cell-based systems, organ-on-a-chip devices that incorporate sensors and monitoring capabilities, as well as microfabrication techniques including bioprinting and photolithography, are discussed. These techniques could be combined to help provide highly predictive drug tests for patient-specific conditions in the near future. |
format | Online Article Text |
id | pubmed-6305315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63053152019-01-07 Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models Torras, Núria García-Díaz, María Fernández-Majada, Vanesa Martínez, Elena Front Bioeng Biotechnol Bioengineering and Biotechnology Epithelial tissues are composed of layers of tightly connected cells shaped into complex three-dimensional (3D) structures such as cysts, tubules, or invaginations. These complex 3D structures are important for organ-specific functions and often create biochemical gradients that guide cell positioning and compartmentalization within the organ. One of the main functions of epithelia is to act as physical barriers that protect the underlying tissues from external insults. In vitro, epithelial barriers are usually mimicked by oversimplified models based on cell lines grown as monolayers on flat surfaces. While useful to answer certain questions, these models cannot fully capture the in vivo organ physiology and often yield poor predictions. In order to progress further in basic and translational research, disease modeling, drug discovery, and regenerative medicine, it is essential to advance the development of new in vitro predictive models of epithelial tissues that are capable of representing the in vivo-like structures and organ functionality more accurately. Here, we review current strategies for obtaining biomimetic systems in the form of advanced in vitro models that allow for more reliable and safer preclinical tests. The current state of the art and potential applications of self-organized cell-based systems, organ-on-a-chip devices that incorporate sensors and monitoring capabilities, as well as microfabrication techniques including bioprinting and photolithography, are discussed. These techniques could be combined to help provide highly predictive drug tests for patient-specific conditions in the near future. Frontiers Media S.A. 2018-12-18 /pmc/articles/PMC6305315/ /pubmed/30619844 http://dx.doi.org/10.3389/fbioe.2018.00197 Text en Copyright © 2018 Torras, García-Díaz, Fernández-Majada and Martínez. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Torras, Núria García-Díaz, María Fernández-Majada, Vanesa Martínez, Elena Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title | Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title_full | Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title_fullStr | Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title_full_unstemmed | Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title_short | Mimicking Epithelial Tissues in Three-Dimensional Cell Culture Models |
title_sort | mimicking epithelial tissues in three-dimensional cell culture models |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305315/ https://www.ncbi.nlm.nih.gov/pubmed/30619844 http://dx.doi.org/10.3389/fbioe.2018.00197 |
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