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Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells
Umbilical cord mesenchymal stem cells (UC-MSCs) have certain advantages over other MSCs and about 300 clinical trials have been registered using UC-MSCs to treat diseases such as osteoarthritis, autoimmune diseases, and degenerative disorders, yet, only limited success has been achieved. One reason...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791785/ https://www.ncbi.nlm.nih.gov/pubmed/33413643 http://dx.doi.org/10.1186/s13287-020-02055-1 |
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author | Zhang, Shaoyang Wang, Jing Yi Li, Baojie Yin, Feng Liu, Huijuan |
author_facet | Zhang, Shaoyang Wang, Jing Yi Li, Baojie Yin, Feng Liu, Huijuan |
author_sort | Zhang, Shaoyang |
collection | PubMed |
description | Umbilical cord mesenchymal stem cells (UC-MSCs) have certain advantages over other MSCs and about 300 clinical trials have been registered using UC-MSCs to treat diseases such as osteoarthritis, autoimmune diseases, and degenerative disorders, yet, only limited success has been achieved. One reason is that in vitro expanded UC-MSCs show tremendous heterogeneity and their relationship to in vivo UC-MSCs remains unknown. Here, we investigated freshly isolated, uncultured UC-MSCs by single-cell RNA sequencing (scRNA-seq) and found two populations of UC-MSCs. Although UC-MSCs share many expressed genes and may have the same origin, they can be clearly separated based on differentially expressed genes including CD73 and other markers. Moreover, group 1 MSCs are enriched in expression of genes in immune response/regulatory activities, muscle cell proliferation and differentiation, stemness, and oxidative stress while group 2 MSCs are enriched with gene expression in extracellular matrix production, osteoblast and chondrocytes differentiation, and bone and cartilage growth. These findings suggest that UC-MSCs should be separated right after isolation and individually expanded in vitro to treat different diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-020-02055-1. |
format | Online Article Text |
id | pubmed-7791785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77917852021-01-11 Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells Zhang, Shaoyang Wang, Jing Yi Li, Baojie Yin, Feng Liu, Huijuan Stem Cell Res Ther Letter Umbilical cord mesenchymal stem cells (UC-MSCs) have certain advantages over other MSCs and about 300 clinical trials have been registered using UC-MSCs to treat diseases such as osteoarthritis, autoimmune diseases, and degenerative disorders, yet, only limited success has been achieved. One reason is that in vitro expanded UC-MSCs show tremendous heterogeneity and their relationship to in vivo UC-MSCs remains unknown. Here, we investigated freshly isolated, uncultured UC-MSCs by single-cell RNA sequencing (scRNA-seq) and found two populations of UC-MSCs. Although UC-MSCs share many expressed genes and may have the same origin, they can be clearly separated based on differentially expressed genes including CD73 and other markers. Moreover, group 1 MSCs are enriched in expression of genes in immune response/regulatory activities, muscle cell proliferation and differentiation, stemness, and oxidative stress while group 2 MSCs are enriched with gene expression in extracellular matrix production, osteoblast and chondrocytes differentiation, and bone and cartilage growth. These findings suggest that UC-MSCs should be separated right after isolation and individually expanded in vitro to treat different diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-020-02055-1. BioMed Central 2021-01-07 /pmc/articles/PMC7791785/ /pubmed/33413643 http://dx.doi.org/10.1186/s13287-020-02055-1 Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter Zhang, Shaoyang Wang, Jing Yi Li, Baojie Yin, Feng Liu, Huijuan Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title | Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title_full | Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title_fullStr | Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title_full_unstemmed | Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title_short | Single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
title_sort | single-cell transcriptome analysis of uncultured human umbilical cord mesenchymal stem cells |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791785/ https://www.ncbi.nlm.nih.gov/pubmed/33413643 http://dx.doi.org/10.1186/s13287-020-02055-1 |
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