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Early megakaryocyte lineage-committed progenitors in adult mouse bone marrow.
Liu, Zixian; Wang, Jinhong; Ma, Yao; Xie, Miner; Wu, Peng; Zhang, Sen; Wang, Xiaofang; Dong, Fang; Cheng, Hui; Zhu, Ping; Han, Mingzhe; Ema, Hideo.
Affiliation
  • Liu Z; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Wang J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Ma Y; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Xie M; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Wu P; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Zhang S; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Wang X; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Dong F; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Cheng H; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Zhu P; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Han M; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
  • Ema H; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Hematological Disorders, Haihe Laboratory of Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Blood Sci ; 6(2): e00187, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38721470
ABSTRACT
Hematopoietic stem cells (HSCs) have been considered to progressively lose their self-renewal and differentiation potentials prior to the commitment to each blood lineage. However, recent studies have suggested that megakaryocyte progenitors (MkPs) are generated at the level of HSCs. In this study, we newly identified early megakaryocyte lineage-committed progenitors (MgPs) mainly in CD201-CD48- cells and CD48+ cells separated from the CD150+CD34-Kit+Sca-1+Lin- HSC population of the bone marrow in adult mice. Single-cell colony assay and single-cell transplantation showed that MgPs, unlike platelet-biased HSCs, had little repopulating potential in vivo, but formed larger megakaryocyte colonies in vitro (on average 8 megakaryocytes per colony) than did previously reported MkPs. Single-cell RNA sequencing supported that HSCs give rise to MkPs through MgPs along a Mk differentiation pathway. Single-cell reverse transcription polymerase chain reaction (RT-PCR) analysis showed that MgPs expressed Mk-related genes, but were transcriptionally heterogenous. Clonal culture of HSCs suggested that MgPs are not direct progeny of HSCs. We propose a differentiation model in which HSCs give rise to MgPs which then give rise to MkPs, supporting a classic model in which Mk-lineage commitment takes place at a late stage of differentiation.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Blood Sci Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Blood Sci Year: 2024 Document type: Article Affiliation country: China