4.7 Article

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

Journal

CELL DISCOVERY
Volume 6, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41421-020-00213-6

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Funding

  1. National Key Research and Development Program of China, Stem Cell and Translational Research [2017YFA0102600]
  2. Strategic Priority Research Program of Chinese Academy of Sciences [XDA16030504]
  3. Science and Technology Planning Project of Guangdong Province, China [2017B030314056]
  4. Frontier and Key Technology Innovation Special Grant from the Department of Science and Technology of Guangdong Province [2016B030230002, 2016B030229008]
  5. National Natural Science Foundation of China [31801220, 31971374]
  6. Guangzhou Science and Technology Program General project [20180304001, 201904020045, 201904010462]
  7. Innovative Team Program of Guangzhou Regenerative Medicine and Health Guangdong Laboratory [2018GZR110104005]
  8. Informationization Special Project of Chinese Academy of Sciences E-Science Application for Knowledge Discovery in Stem Cells [XXH13506-203]
  9. Open Research Funds of the State Key Laboratory of Ophthalmology [2019KF06]
  10. Guangdong Province Special Program for Outstanding Talents [2019JC05Y463]

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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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