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RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate
Due to serious adverse effects, many of the approved anti-obesity medicines have been withdrawn, and the selection of safer natural ingredients is of great interest. Epigallocatechin gallate (EGCG) is one of the major green tea catechins, and has been demonstrated to possess an anti-obesity function...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826391/ https://www.ncbi.nlm.nih.gov/pubmed/35136080 http://dx.doi.org/10.1038/s41597-022-01149-0 |
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author | Zhang, Pengpeng Wu, Wei Du, Chunyu Ji, Xiang Wang, Yaling Han, Qiu Xu, Hiaxia Li, Cencen Xu, Yongjie |
author_facet | Zhang, Pengpeng Wu, Wei Du, Chunyu Ji, Xiang Wang, Yaling Han, Qiu Xu, Hiaxia Li, Cencen Xu, Yongjie |
author_sort | Zhang, Pengpeng |
collection | PubMed |
description | Due to serious adverse effects, many of the approved anti-obesity medicines have been withdrawn, and the selection of safer natural ingredients is of great interest. Epigallocatechin gallate (EGCG) is one of the major green tea catechins, and has been demonstrated to possess an anti-obesity function by regulating both white and brown adipose tissue activity. However, there are currently no publicly available studies describing the effects of EGCG on the two distinct adipose tissue transcriptomes. The stromal vascular fraction (SVF) cell derived from adipose tissue is a classic cell model for studying adipogenesis and fat accumulation. In the current study, primary WAT and BAT SVF cells were isolated and induced to adipogenic differentiation in the presence or absence of EGCG. RNA-seq was used to determine genes regulated by EGCG and identify the key differences between the two functionally distinct adipose tissues. Taken together, we provide detailed stage- and tissue-specific gene expression profiles affected by EGCG. These data will be valuable for obesity-related clinical/basic research. |
format | Online Article Text |
id | pubmed-8826391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88263912022-02-17 RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate Zhang, Pengpeng Wu, Wei Du, Chunyu Ji, Xiang Wang, Yaling Han, Qiu Xu, Hiaxia Li, Cencen Xu, Yongjie Sci Data Data Descriptor Due to serious adverse effects, many of the approved anti-obesity medicines have been withdrawn, and the selection of safer natural ingredients is of great interest. Epigallocatechin gallate (EGCG) is one of the major green tea catechins, and has been demonstrated to possess an anti-obesity function by regulating both white and brown adipose tissue activity. However, there are currently no publicly available studies describing the effects of EGCG on the two distinct adipose tissue transcriptomes. The stromal vascular fraction (SVF) cell derived from adipose tissue is a classic cell model for studying adipogenesis and fat accumulation. In the current study, primary WAT and BAT SVF cells were isolated and induced to adipogenic differentiation in the presence or absence of EGCG. RNA-seq was used to determine genes regulated by EGCG and identify the key differences between the two functionally distinct adipose tissues. Taken together, we provide detailed stage- and tissue-specific gene expression profiles affected by EGCG. These data will be valuable for obesity-related clinical/basic research. Nature Publishing Group UK 2022-02-08 /pmc/articles/PMC8826391/ /pubmed/35136080 http://dx.doi.org/10.1038/s41597-022-01149-0 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) applies to the metadata files associated with this article. |
spellingShingle | Data Descriptor Zhang, Pengpeng Wu, Wei Du, Chunyu Ji, Xiang Wang, Yaling Han, Qiu Xu, Hiaxia Li, Cencen Xu, Yongjie RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title | RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title_full | RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title_fullStr | RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title_full_unstemmed | RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title_short | RNA-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
title_sort | rna-seq profiling of white and brown adipocyte differentiation treated with epigallocatechin gallate |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826391/ https://www.ncbi.nlm.nih.gov/pubmed/35136080 http://dx.doi.org/10.1038/s41597-022-01149-0 |
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