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Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs
Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) through epigenetic manipulation. While the essential role of miRNA in reprogramming and maintaining pluripotency is well studied, little is known about the functions of miRNA from exosomes in this context. To fill this res...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495316/ https://www.ncbi.nlm.nih.gov/pubmed/37696871 http://dx.doi.org/10.1038/s41597-023-02493-5 |
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author | Yu, Chunlai Zhang, Mei Xiong, Yucui Wang, Qizheng Wang, Yuanhua Wu, Shaoling Hussain, Sajjad Wang, Yan Zhang, Zhizhong Rao, Nini Zhang, Sheng Zhang, Xiao |
author_facet | Yu, Chunlai Zhang, Mei Xiong, Yucui Wang, Qizheng Wang, Yuanhua Wu, Shaoling Hussain, Sajjad Wang, Yan Zhang, Zhizhong Rao, Nini Zhang, Sheng Zhang, Xiao |
author_sort | Yu, Chunlai |
collection | PubMed |
description | Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) through epigenetic manipulation. While the essential role of miRNA in reprogramming and maintaining pluripotency is well studied, little is known about the functions of miRNA from exosomes in this context. To fill this research gap,we comprehensively obtained the 17 sets of cellular mRNA transcriptomic data with 3.93 × 10(10 )bp raw reads and 18 sets of exosomal miRNA transcriptomic data with 2.83 × 10(7 )bp raw reads from three categories of human somatic cells: peripheral blood mononuclear cells (PBMCs), skin fibroblasts(SFs) and urine cells (UCs), along with their derived iPSCs. Additionally, differentially expressed molecules of each category were identified and used to perform gene set enrichment analysis. Our study provides sets of comparative transcriptomic data of cellular mRNA and exosomal miRNA from three categories of human tissue with three individual biological controls in studies of iPSCs generation, which will contribute to a better understanding of donor cell variation in functional epigenetic regulation and differentiation bias in iPSCs. |
format | Online Article Text |
id | pubmed-10495316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104953162023-09-13 Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs Yu, Chunlai Zhang, Mei Xiong, Yucui Wang, Qizheng Wang, Yuanhua Wu, Shaoling Hussain, Sajjad Wang, Yan Zhang, Zhizhong Rao, Nini Zhang, Sheng Zhang, Xiao Sci Data Data Descriptor Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) through epigenetic manipulation. While the essential role of miRNA in reprogramming and maintaining pluripotency is well studied, little is known about the functions of miRNA from exosomes in this context. To fill this research gap,we comprehensively obtained the 17 sets of cellular mRNA transcriptomic data with 3.93 × 10(10 )bp raw reads and 18 sets of exosomal miRNA transcriptomic data with 2.83 × 10(7 )bp raw reads from three categories of human somatic cells: peripheral blood mononuclear cells (PBMCs), skin fibroblasts(SFs) and urine cells (UCs), along with their derived iPSCs. Additionally, differentially expressed molecules of each category were identified and used to perform gene set enrichment analysis. Our study provides sets of comparative transcriptomic data of cellular mRNA and exosomal miRNA from three categories of human tissue with three individual biological controls in studies of iPSCs generation, which will contribute to a better understanding of donor cell variation in functional epigenetic regulation and differentiation bias in iPSCs. Nature Publishing Group UK 2023-09-11 /pmc/articles/PMC10495316/ /pubmed/37696871 http://dx.doi.org/10.1038/s41597-023-02493-5 Text en © The Author(s) 2023 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 | Data Descriptor Yu, Chunlai Zhang, Mei Xiong, Yucui Wang, Qizheng Wang, Yuanhua Wu, Shaoling Hussain, Sajjad Wang, Yan Zhang, Zhizhong Rao, Nini Zhang, Sheng Zhang, Xiao Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title | Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title_full | Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title_fullStr | Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title_full_unstemmed | Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title_short | Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs |
title_sort | comparison of mirna transcriptome of exosomes in three categories of somatic cells with derived ipscs |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495316/ https://www.ncbi.nlm.nih.gov/pubmed/37696871 http://dx.doi.org/10.1038/s41597-023-02493-5 |
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