Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rogal, Julia, Roosz, Julia, Teufel, Claudia, Cipriano, Madalena, Xu, Raylin, Eisler, Wiebke, Weiss, Martin, Schenke‐Layland, Katja, Loskill, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784731964745449472
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
work_keys_str_mv AT rogaljulia autologoushumanimmunocompetentwhiteadiposetissueonchip
AT rooszjulia autologoushumanimmunocompetentwhiteadiposetissueonchip
AT teufelclaudia autologoushumanimmunocompetentwhiteadiposetissueonchip
AT ciprianomadalena autologoushumanimmunocompetentwhiteadiposetissueonchip
AT xuraylin autologoushumanimmunocompetentwhiteadiposetissueonchip
AT eislerwiebke autologoushumanimmunocompetentwhiteadiposetissueonchip
AT weissmartin autologoushumanimmunocompetentwhiteadiposetissueonchip
AT schenkelaylandkatja autologoushumanimmunocompetentwhiteadiposetissueonchip
AT loskillpeter autologoushumanimmunocompetentwhiteadiposetissueonchip