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Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism
Adipose tissue is an organized endocrine organ with important metabolic and immunological functions and immune cell-adipocyte crosstalk is known to drive various disease pathologies. Suitable 3D adipose tissue organoid models often lack resident immune cell populations and therefore require the addi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713299/ https://www.ncbi.nlm.nih.gov/pubmed/33273595 http://dx.doi.org/10.1038/s41598-020-78015-9 |
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author | Taylor, Jacqueline Sellin, Julia Kuerschner, Lars Krähl, Lennart Majlesain, Yasmin Förster, Irmgard Thiele, Christoph Weighardt, Heike Weber, Elvira |
author_facet | Taylor, Jacqueline Sellin, Julia Kuerschner, Lars Krähl, Lennart Majlesain, Yasmin Förster, Irmgard Thiele, Christoph Weighardt, Heike Weber, Elvira |
author_sort | Taylor, Jacqueline |
collection | PubMed |
description | Adipose tissue is an organized endocrine organ with important metabolic and immunological functions and immune cell-adipocyte crosstalk is known to drive various disease pathologies. Suitable 3D adipose tissue organoid models often lack resident immune cell populations and therefore require the addition of immune cells isolated from other organs. We have created the first 3D adipose tissue organoid model which could contain and maintain resident immune cell populations of the stromal vascular fraction (SVF) and proved to be effective in studying adipose tissue biology in a convenient manner. Macrophage and mast cell populations were successfully confirmed within our organoid model and were maintained in culture without the addition of growth factors. We demonstrated the suitability of our model for monitoring the lipidome during adipocyte differentiation in vitro and confirmed that this model reflects the physiological lipidome better than standard 2D cultures. In addition, we applied mass spectrometry-based lipidomics to track lipidomic changes in the lipidome upon dietary and immunomodulatory interventions. We conclude that this model represents a valuable tool for immune-metabolic research. |
format | Online Article Text |
id | pubmed-7713299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77132992020-12-03 Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism Taylor, Jacqueline Sellin, Julia Kuerschner, Lars Krähl, Lennart Majlesain, Yasmin Förster, Irmgard Thiele, Christoph Weighardt, Heike Weber, Elvira Sci Rep Article Adipose tissue is an organized endocrine organ with important metabolic and immunological functions and immune cell-adipocyte crosstalk is known to drive various disease pathologies. Suitable 3D adipose tissue organoid models often lack resident immune cell populations and therefore require the addition of immune cells isolated from other organs. We have created the first 3D adipose tissue organoid model which could contain and maintain resident immune cell populations of the stromal vascular fraction (SVF) and proved to be effective in studying adipose tissue biology in a convenient manner. Macrophage and mast cell populations were successfully confirmed within our organoid model and were maintained in culture without the addition of growth factors. We demonstrated the suitability of our model for monitoring the lipidome during adipocyte differentiation in vitro and confirmed that this model reflects the physiological lipidome better than standard 2D cultures. In addition, we applied mass spectrometry-based lipidomics to track lipidomic changes in the lipidome upon dietary and immunomodulatory interventions. We conclude that this model represents a valuable tool for immune-metabolic research. Nature Publishing Group UK 2020-12-03 /pmc/articles/PMC7713299/ /pubmed/33273595 http://dx.doi.org/10.1038/s41598-020-78015-9 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Taylor, Jacqueline Sellin, Julia Kuerschner, Lars Krähl, Lennart Majlesain, Yasmin Förster, Irmgard Thiele, Christoph Weighardt, Heike Weber, Elvira Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title | Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title_full | Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title_fullStr | Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title_full_unstemmed | Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title_short | Generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
title_sort | generation of immune cell containing adipose organoids for in vitro analysis of immune metabolism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713299/ https://www.ncbi.nlm.nih.gov/pubmed/33273595 http://dx.doi.org/10.1038/s41598-020-78015-9 |
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