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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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