TY - JOUR
T1 - Identification of unipotent megakaryocyte progenitors in human hematopoiesis
AU - Miyawaki, Kohta
AU - Iwasaki, Hiromi
AU - Jiromaru, Takashi
AU - Kusumoto, Hirotake
AU - Yurino, Ayano
AU - Sugio, Takeshi
AU - Uehara, Yasufumi
AU - Odawara, Jun
AU - Daitoku, Shinya
AU - Kunisaki, Yuya
AU - Mori, Yasuo
AU - Arinobu, Yojiro
AU - Tsuzuki, Hirofumi
AU - Kikushige, Yoshikane
AU - Iino, Tadafumi
AU - Kato, Koji
AU - Takenaka, Katsuto
AU - Miyamoto, Toshihiro
AU - Maeda, Takahiro
AU - Akashi, Koichi
N1 - Publisher Copyright:
© 2017 by The American Society of Hematology.
PY - 2017/6/22
Y1 - 2017/6/22
N2 - The developmental pathway for human megakaryocytes remains unclear, and the definition of pure unipotent megakaryocyte progenitor is still controversial. Using single-cell transcriptome analysis, we have identified a cluster of cells within immature hematopoietic stem- and progenitor-cell populations that specifically expresses genes related to the megakaryocyte lineage. We used CD41 as a positive marker to identify these cells within the CD34+CD38+IL-3RαdimCD45RA- common myeloid progenitor (CMP) population. These cells lacked erythroid and granulocyte-macrophage potential but exhibited robust differentiation into the megakaryocyte lineage at a high frequency, both in vivo and in vitro. The efficiency and expansion potential of these cells exceeded those of conventional bipotent megakaryocyte/erythrocyte progenitors. Accordingly, the CD41+ CMP was defined as a unipotent megakaryocyte progenitor (MegP) that is likely to represent the major pathway for human megakaryopoiesis, independent of canonical megakaryocyte-erythroid lineage bifurcation. In the bone marrow of patients with essential thrombocythemia, the MegP population was significantly expanded in the context of a high burden of Janus kinase 2 mutations. Thus, the prospectively isolatable and functionally homogeneous human MegP will be useful for the elucidation of the mechanisms underlying normal and malignant human hematopoiesis. (Blood. 2017;129(25): 3332-3343).
AB - The developmental pathway for human megakaryocytes remains unclear, and the definition of pure unipotent megakaryocyte progenitor is still controversial. Using single-cell transcriptome analysis, we have identified a cluster of cells within immature hematopoietic stem- and progenitor-cell populations that specifically expresses genes related to the megakaryocyte lineage. We used CD41 as a positive marker to identify these cells within the CD34+CD38+IL-3RαdimCD45RA- common myeloid progenitor (CMP) population. These cells lacked erythroid and granulocyte-macrophage potential but exhibited robust differentiation into the megakaryocyte lineage at a high frequency, both in vivo and in vitro. The efficiency and expansion potential of these cells exceeded those of conventional bipotent megakaryocyte/erythrocyte progenitors. Accordingly, the CD41+ CMP was defined as a unipotent megakaryocyte progenitor (MegP) that is likely to represent the major pathway for human megakaryopoiesis, independent of canonical megakaryocyte-erythroid lineage bifurcation. In the bone marrow of patients with essential thrombocythemia, the MegP population was significantly expanded in the context of a high burden of Janus kinase 2 mutations. Thus, the prospectively isolatable and functionally homogeneous human MegP will be useful for the elucidation of the mechanisms underlying normal and malignant human hematopoiesis. (Blood. 2017;129(25): 3332-3343).
UR - http://www.scopus.com/inward/record.url?scp=85021635830&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85021635830&partnerID=8YFLogxK
U2 - 10.1182/blood-2016-09-741611
DO - 10.1182/blood-2016-09-741611
M3 - Article
C2 - 28336526
AN - SCOPUS:85021635830
SN - 0006-4971
VL - 129
SP - 3332
EP - 3343
JO - Blood
JF - Blood
IS - 25
ER -