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Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail
Identification of effective culture conditions to maintain and possibly expand human HSPCs in vitro is an important goal. Recent advances highlight the efficacy of chemicals in maintaining and converting cell fates. We screened 186 chemicals and found that a combination of CHIR-99021, Forskolin and...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206058/ https://www.ncbi.nlm.nih.gov/pubmed/30393564 http://dx.doi.org/10.1038/s41421-018-0059-5 |
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author | Jiang, Mengmeng Chen, Haide Lai, Shujing Wang, Renying Qiu, Yunfei Ye, Fang Fei, Lijiang Sun, Huiyu Xu, Yang Jiang, Xinyi Zhou, Ziming Zhang, Tingyue Li, Yanwei Xie, Jin Fang, Qun Gale, Robert Peter Han, Xiaoping Huang, He Guo, Guoji |
author_facet | Jiang, Mengmeng Chen, Haide Lai, Shujing Wang, Renying Qiu, Yunfei Ye, Fang Fei, Lijiang Sun, Huiyu Xu, Yang Jiang, Xinyi Zhou, Ziming Zhang, Tingyue Li, Yanwei Xie, Jin Fang, Qun Gale, Robert Peter Han, Xiaoping Huang, He Guo, Guoji |
author_sort | Jiang, Mengmeng |
collection | PubMed |
description | Identification of effective culture conditions to maintain and possibly expand human HSPCs in vitro is an important goal. Recent advances highlight the efficacy of chemicals in maintaining and converting cell fates. We screened 186 chemicals and found that a combination of CHIR-99021, Forskolin and OAC1 (CFO) maintained human CD34-positive cells in vitro. Efficiency of the culture system was characterized using flow cytometry for CD34-positive cells, a colony-forming assay and xeno-transplants. We found that human CD34-positive cells treated with this combination had enhanced expression of human HSPC markers and increased haematopoietic re-populating ability in immune-deficient mice. Single-cell RNA-seq analyses showed that the in vitro cultured human CD34-positive cells were heterogeneous. We found that CFO supports maintenance of human CD34-positive cells by activating HOXA9, GATA2 and AKT-cAMP signaling pathway. These data have implications in therapies requiring maintenance and/or expansion of human HSPCs. |
format | Online Article Text |
id | pubmed-6206058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62060582018-11-02 Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail Jiang, Mengmeng Chen, Haide Lai, Shujing Wang, Renying Qiu, Yunfei Ye, Fang Fei, Lijiang Sun, Huiyu Xu, Yang Jiang, Xinyi Zhou, Ziming Zhang, Tingyue Li, Yanwei Xie, Jin Fang, Qun Gale, Robert Peter Han, Xiaoping Huang, He Guo, Guoji Cell Discov Article Identification of effective culture conditions to maintain and possibly expand human HSPCs in vitro is an important goal. Recent advances highlight the efficacy of chemicals in maintaining and converting cell fates. We screened 186 chemicals and found that a combination of CHIR-99021, Forskolin and OAC1 (CFO) maintained human CD34-positive cells in vitro. Efficiency of the culture system was characterized using flow cytometry for CD34-positive cells, a colony-forming assay and xeno-transplants. We found that human CD34-positive cells treated with this combination had enhanced expression of human HSPC markers and increased haematopoietic re-populating ability in immune-deficient mice. Single-cell RNA-seq analyses showed that the in vitro cultured human CD34-positive cells were heterogeneous. We found that CFO supports maintenance of human CD34-positive cells by activating HOXA9, GATA2 and AKT-cAMP signaling pathway. These data have implications in therapies requiring maintenance and/or expansion of human HSPCs. Nature Publishing Group UK 2018-10-30 /pmc/articles/PMC6206058/ /pubmed/30393564 http://dx.doi.org/10.1038/s41421-018-0059-5 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Jiang, Mengmeng Chen, Haide Lai, Shujing Wang, Renying Qiu, Yunfei Ye, Fang Fei, Lijiang Sun, Huiyu Xu, Yang Jiang, Xinyi Zhou, Ziming Zhang, Tingyue Li, Yanwei Xie, Jin Fang, Qun Gale, Robert Peter Han, Xiaoping Huang, He Guo, Guoji Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title | Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title_full | Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title_fullStr | Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title_full_unstemmed | Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title_short | Maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
title_sort | maintenance of human haematopoietic stem and progenitor cells in vitro using a chemical cocktail |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206058/ https://www.ncbi.nlm.nih.gov/pubmed/30393564 http://dx.doi.org/10.1038/s41421-018-0059-5 |
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