CD62L expression level determines the cell fate of myeloid progenitors.
CD62L expression level determines the cell fate of myeloid progenitors.
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DOI:
10.1016/j.stemcr.2021.10.012
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发表时间:
2021-12-14
影响因子:
5.9
通讯作者:
Kurokawa M
中科院分区:
文献类型:
--
作者:
Ito Y;Nakahara F;Kagoya Y;Kurokawa M
Hematopoietic cells differentiate through several progenitors in a hierarchical manner, and recent single-cell analyses have revealed substantial heterogeneity within each progenitor. Although common myeloid progenitors (CMPs) are defined as a multipotent cell population that can differentiate into granulocyte-monocyte progenitors (GMPs) and megakaryocyte-erythrocyte progenitors (MEPs), and GMPs generate neutrophils and monocytes, these myeloid progenitors must contain some lineage-committed progenitors. Through gene expression analysis at single-cell levels, we identified CD62L as a marker to reveal the heterogeneity. We confirmed that CD62L-negative CMPs represent “bona fide” CMPs, whereas CD62L-high CMPs are mostly restricted to GMP potentials both in mice and humans. In addition, we identified CD62L-negative GMPs as the most immature subsets in GMPs and Ly6C+CD62L-intermediate and Ly6C+CD62L-high GMPs are skewed to neutrophil and monocyte differentiation in mice, respectively. Our findings contribute to more profound understanding about the mechanism of myeloid differentiation. CD62L-high CMPs are mostly restricted to GMP potentials both in mice and humans CD62L-neg GMPs are most immature in murine GMPs Ly6C+/CD62L-int GMPs are skewed to neutrophil differentiation in mice Ly6C+/CD62L-high GMPs are skewed to monocyte differentiation in mice Kurokawa and colleagues identify CD62L as a marker to reveal the heterogeneity of common myeloid progenitors (CMPs) and granulocyte-monocyte progenitors (GMPs) through gene expression analysis at single-cell levels. CD62L-high CMPs are mostly restricted to GMP potentials, and Ly6C+/CD62L-int and -high GMPs are skewed to neutrophil and monocyte differentiation, respectively. These findings provide more profound understanding about myeloid differentiation.
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DOI:
10.1073/pnas.1512076112
发表时间:
2015-08-04
影响因子:
11.1
作者:
Mori, Yasuo;Chen, James Y.;Weissman, Irving L.
通讯作者:
Weissman, Irving L.
DOI:
10.1002/stem.1985
发表时间:
2015-07
期刊:
Stem cells (Dayton, Ohio)
影响因子:
--
作者:
Nishikii H;Kanazawa Y;Umemoto T;Goltsev Y;Matsuzaki Y;Matsushita K;Yamato M;Nolan GP;Negrin R;Chiba S
通讯作者:
Chiba S
影响因子:
24.8
作者:
Drissen, Roy;Thongjuea, Supat;Nerlov, Claus
通讯作者:
Nerlov, Claus
影响因子:
8
作者:
Cantor, AB;Orkin, SH
通讯作者:
Orkin, SH
影响因子:
11.4
作者:
Drexler, HG;Zaborski, M;Quentmeier, H
通讯作者:
Quentmeier, H