Early differentiation of committed erythroid cells defined by miR-144/451 expression.

IF 5.3 2区 生物学 Q2 CELL BIOLOGY
Xiaohong Li, Yong Dong, Pan Xu, Wencui Sun, Yuan Xue, Ya Zhou, Mowen Lai, Yonggang Zhang, Feng Ma
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Abstract

Before committing to an erythroid cell lineage, hematopoietic stem cells differentiate along a myeloid cell pathway to generate megakaryocyte-erythroid biopotential progenitor cells in bone marrow. Recent studies suggest that erythroid progenitors (EryPs) could be generated at the level of common myeloid progenitors (CMPs). However, due to a lack of suitable markers, little is known about the early differentiation of these committed EryP cells during CMP development. Herein, using miR-144/451-eGFP knock-in mice, we found that early differentiation of committed erythroid cells could be defined by miR-144/451 expression within CMPs. Single-cell RNA sequencing showed that miR-144/451+ progenitors had obvious differentiation characteristics of erythroid lineage cells and diverged from megakaryocyte and other myeloid cell lineages. These progenitors exclusively gave rise to erythroid cells, both in vitro and in vivo, and the commitment to an erythroid cell lineage was accompanied by loss of CD53 expression. Our findings will facilitate further understanding of the molecular mechanisms governing erythroid development and support the identification of therapeutic targets for diseases related to erythrocyte development.

由miR-144/451表达决定的红细胞早期分化。
造血干细胞在分化为红系细胞之前,沿着髓系细胞途径分化,在骨髓中产生巨核细胞-红系生物潜能祖细胞。最近的研究表明,红细胞祖细胞(EryPs)可以在普通髓系祖细胞(CMPs)水平上产生。然而,由于缺乏合适的标记物,在CMP发育过程中,对这些承诺的EryP细胞的早期分化知之甚少。在这里,我们使用miR-144/451- egfp敲入小鼠,我们发现在cmp中miR-144/451的表达可以定义红系细胞的早期分化。单细胞RNA测序显示,miR-144/451+祖细胞具有明显的红系细胞分化特征,并与巨核细胞和其他髓系细胞分化。在体外和体内,这些祖细胞只产生红系细胞,而红系细胞谱系的形成伴随着CD53表达的缺失。我们的发现将有助于进一步了解控制红细胞发育的分子机制,并支持确定与红细胞发育相关疾病的治疗靶点。
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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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