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Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip
Obesity and associated diseases, such as diabetes, have reached epidemic proportions globally. In this era of “diabesity”, white adipose tissue (WAT) has become a target of high interest for therapeutic strategies. To gain insights into mechanisms of adipose (patho‐)physiology, researchers tradition...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218765/ https://www.ncbi.nlm.nih.gov/pubmed/35466539 http://dx.doi.org/10.1002/advs.202104451 |
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author | Rogal, Julia Roosz, Julia Teufel, Claudia Cipriano, Madalena Xu, Raylin Eisler, Wiebke Weiss, Martin Schenke‐Layland, Katja Loskill, Peter |
author_facet | Rogal, Julia Roosz, Julia Teufel, Claudia Cipriano, Madalena Xu, Raylin Eisler, Wiebke Weiss, Martin Schenke‐Layland, Katja Loskill, Peter |
author_sort | Rogal, Julia |
collection | PubMed |
description | Obesity and associated diseases, such as diabetes, have reached epidemic proportions globally. In this era of “diabesity”, white adipose tissue (WAT) has become a target of high interest for therapeutic strategies. To gain insights into mechanisms of adipose (patho‐)physiology, researchers traditionally relied on animal models. Leveraging Organ‐on‐Chip technology, a microphysiological in vitro model of human WAT is introduced: a tailored microfluidic platform featuring vasculature‐like perfusion that integrates 3D tissues comprising all major WAT‐associated cellular components (mature adipocytes, organotypic endothelial barriers, stromovascular cells including adipose tissue macrophages) in an autologous manner and recapitulates pivotal WAT functions, such as energy storage and mobilization as well as endocrine and immunomodulatory activities. A precisely controllable bottom‐up approach enables the generation of a multitude of replicates per donor circumventing inter‐donor variability issues and paving the way for personalized medicine. Moreover, it allows to adjust the model's degree of complexity via a flexible mix‐and‐match approach. This WAT‐on‐Chip system constitutes the first human‐based, autologous, and immunocompetent in vitro adipose tissue model that recapitulates almost full tissue heterogeneity and can become a powerful tool for human‐relevant research in the field of metabolism and its associated diseases as well as for compound testing and personalized‐ and precision medicine applications. |
format | Online Article Text |
id | pubmed-9218765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92187652022-06-29 Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip Rogal, Julia Roosz, Julia Teufel, Claudia Cipriano, Madalena Xu, Raylin Eisler, Wiebke Weiss, Martin Schenke‐Layland, Katja Loskill, Peter Adv Sci (Weinh) Research Articles Obesity and associated diseases, such as diabetes, have reached epidemic proportions globally. In this era of “diabesity”, white adipose tissue (WAT) has become a target of high interest for therapeutic strategies. To gain insights into mechanisms of adipose (patho‐)physiology, researchers traditionally relied on animal models. Leveraging Organ‐on‐Chip technology, a microphysiological in vitro model of human WAT is introduced: a tailored microfluidic platform featuring vasculature‐like perfusion that integrates 3D tissues comprising all major WAT‐associated cellular components (mature adipocytes, organotypic endothelial barriers, stromovascular cells including adipose tissue macrophages) in an autologous manner and recapitulates pivotal WAT functions, such as energy storage and mobilization as well as endocrine and immunomodulatory activities. A precisely controllable bottom‐up approach enables the generation of a multitude of replicates per donor circumventing inter‐donor variability issues and paving the way for personalized medicine. Moreover, it allows to adjust the model's degree of complexity via a flexible mix‐and‐match approach. This WAT‐on‐Chip system constitutes the first human‐based, autologous, and immunocompetent in vitro adipose tissue model that recapitulates almost full tissue heterogeneity and can become a powerful tool for human‐relevant research in the field of metabolism and its associated diseases as well as for compound testing and personalized‐ and precision medicine applications. John Wiley and Sons Inc. 2022-04-24 /pmc/articles/PMC9218765/ /pubmed/35466539 http://dx.doi.org/10.1002/advs.202104451 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Rogal, Julia Roosz, Julia Teufel, Claudia Cipriano, Madalena Xu, Raylin Eisler, Wiebke Weiss, Martin Schenke‐Layland, Katja Loskill, Peter Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title | Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title_full | Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title_fullStr | Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title_full_unstemmed | Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title_short | Autologous Human Immunocompetent White Adipose Tissue‐on‐Chip |
title_sort | autologous human immunocompetent white adipose tissue‐on‐chip |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218765/ https://www.ncbi.nlm.nih.gov/pubmed/35466539 http://dx.doi.org/10.1002/advs.202104451 |
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