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Progenitor cells from brown adipose tissue undergo neurogenic differentiation
Multipotent cells derived from white adipose tissue have been shown to differentiate into multiple lineages including neurogenic lineages. However, the high innervation of brown adipose tissue by the sympathetic nervous system suggest it might be a better source of neural precursor cells. To investi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980074/ https://www.ncbi.nlm.nih.gov/pubmed/35379860 http://dx.doi.org/10.1038/s41598-022-09382-8 |
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author | Jumabay, Medet Zhang, Li Yao, Jiayi Boström, Kristina I. |
author_facet | Jumabay, Medet Zhang, Li Yao, Jiayi Boström, Kristina I. |
author_sort | Jumabay, Medet |
collection | PubMed |
description | Multipotent cells derived from white adipose tissue have been shown to differentiate into multiple lineages including neurogenic lineages. However, the high innervation of brown adipose tissue by the sympathetic nervous system suggest it might be a better source of neural precursor cells. To investigate potential differences between white and brown progenitors, we cultured white and brown dedifferentiated fat (wDFAT and brDFAT) cells from mouse and human adipose tissue and compared marker expression of neural precursors, and neuronal and glial cells, using fluorescence-activated cell sorting, bright-field imaging, immunofluorescence, and RNA analysis by qPCR. The results showed that both wDFAT and brDFAT cells had the capacity to generate neuronal and glial-like cells under neurogenic conditions. However, the brDFAT cells exhibited enhanced propensity for neurogenic differentiation. The neurogenic cells were at least in part derived from Adiponectin-expressing cells. TdTomato-expressing cells derived from Adiponectin (Adipoq) Cre (ERT2) -tdTomato (flox/flox) mice gave rise to individual cells and cell clusters with neurogenic characteristics. Moreover, human brDFAT cells demonstrated a similar ability to undergo neurogenic differentiation after treatment with neurogenic medium, as assessed by immunofluorescence and qPCR. Together, our results support that brDFAT cells have ability to undergo neurogenic differentiation. |
format | Online Article Text |
id | pubmed-8980074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89800742022-04-06 Progenitor cells from brown adipose tissue undergo neurogenic differentiation Jumabay, Medet Zhang, Li Yao, Jiayi Boström, Kristina I. Sci Rep Article Multipotent cells derived from white adipose tissue have been shown to differentiate into multiple lineages including neurogenic lineages. However, the high innervation of brown adipose tissue by the sympathetic nervous system suggest it might be a better source of neural precursor cells. To investigate potential differences between white and brown progenitors, we cultured white and brown dedifferentiated fat (wDFAT and brDFAT) cells from mouse and human adipose tissue and compared marker expression of neural precursors, and neuronal and glial cells, using fluorescence-activated cell sorting, bright-field imaging, immunofluorescence, and RNA analysis by qPCR. The results showed that both wDFAT and brDFAT cells had the capacity to generate neuronal and glial-like cells under neurogenic conditions. However, the brDFAT cells exhibited enhanced propensity for neurogenic differentiation. The neurogenic cells were at least in part derived from Adiponectin-expressing cells. TdTomato-expressing cells derived from Adiponectin (Adipoq) Cre (ERT2) -tdTomato (flox/flox) mice gave rise to individual cells and cell clusters with neurogenic characteristics. Moreover, human brDFAT cells demonstrated a similar ability to undergo neurogenic differentiation after treatment with neurogenic medium, as assessed by immunofluorescence and qPCR. Together, our results support that brDFAT cells have ability to undergo neurogenic differentiation. Nature Publishing Group UK 2022-04-04 /pmc/articles/PMC8980074/ /pubmed/35379860 http://dx.doi.org/10.1038/s41598-022-09382-8 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jumabay, Medet Zhang, Li Yao, Jiayi Boström, Kristina I. Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title | Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title_full | Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title_fullStr | Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title_full_unstemmed | Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title_short | Progenitor cells from brown adipose tissue undergo neurogenic differentiation |
title_sort | progenitor cells from brown adipose tissue undergo neurogenic differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980074/ https://www.ncbi.nlm.nih.gov/pubmed/35379860 http://dx.doi.org/10.1038/s41598-022-09382-8 |
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