Characterization and generation of human definitive multipotent hematopoietic stem/progenitor cells

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作者
Yanling Zhu
Tianyu Wang
Jiaming Gu
Ke Huang
Tian Zhang
Zhishuai Zhang
He Liu
Jun Tang
Yuchan Mai
Yanqi Zhang
Yuhang Li
Yashu Feng
Baoqiang Kang
Jinbing Li
Yongli Shan
Qianyu Chen
Jian Zhang
Bing Long
Junwei Wang
Minghui Gao
Di Zhang
Min Zhou
Xiaofen Zhong
Jiekai Chen
Duanqing Pei
Jinfu Nie
Bing Liu
Guangjin Pan
机构
[1] Guangzhou Medical University,CAS Key Laboratory of Regenerative Biology, Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences
[2] Chinese Academy of Sciences,Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health
[3] University of Chinese Academy of Sciences,Department of Hematology
[4] The Third Affiliated Hospital,Hefei Institute of Stem Cell and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health
[5] Sun Yat-sen University,Institute for Stem Cell and Regeneration
[6] State Key Laboratory of Experimental Hematology,undefined
[7] Fifth Medical Center of Chinese PLA General Hospital,undefined
[8] Chinese Academy of Sciences,undefined
[9] Chinese Academy of Sciences,undefined
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摘要
Definitive hematopoiesis generates hematopoietic stem/progenitor cells (HSPCs) that give rise to all mature blood and immune cells, but remains poorly defined in human. Here, we resolve human hematopoietic populations at the earliest hematopoiesis stage by single-cell RNA-seq. We characterize the distinct molecular profiling between early primitive and definitive hematopoiesis in both human embryonic stem cell (hESC) differentiation and early embryonic development. We identify CD44 to specifically discriminate definitive hematopoiesis and generate definitive HSPCs from hESCs. The multipotency of hESCs-derived HSPCs for various blood and immune cells is validated by single-cell clonal assay. Strikingly, these hESCs-derived HSPCs give rise to blood and lymphoid lineages in vivo. Lastly, we characterize gene-expression dynamics in definitive and primitive hematopoiesis and reveal an unreported role of ROCK-inhibition in enhancing human definitive hematopoiesis. Our study provides a prospect for understanding human early hematopoiesis and a firm basis for generating blood and immune cells for clinical purposes.
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