| Literature DB >> 31851939 |
Tsuyoshi Fukushima1, Yosuke Tanaka2, Fiona K Hamey3, Chih-Hsiang Chang4, Toshihiko Oki5, Shuhei Asada1, Yasutaka Hayashi1, Takeshi Fujino1, Taishi Yonezawa1, Reina Takeda1, Kimihito Cojin Kawabata6, Tomofusa Fukuyama1, Terumasa Umemoto7, Keiyo Takubo8, Hitoshi Takizawa7, Susumu Goyama1, Yasushi Ishihama4, Hiroaki Honda9, Berthold Göttgens3, Toshio Kitamura1.
Abstract
Quiescent hematopoietic stem cells (HSCs) are typically dormant, and only a few quiescent HSCs are active. The relationship between "dormant" and "active" HSCs remains unresolved. Here we generate a G0 marker (G0M) mouse line that visualizes quiescent cells and identify a small population of active HSCs (G0Mlow), which are distinct from dormant HSCs (G0Mhigh), within the conventional quiescent HSC fraction. Single-cell RNA-seq analyses show that the gene expression profiles of these populations are nearly identical but differ in their Cdk4/6 activity. Furthermore, high-throughput small-molecule screening reveals that high concentrations of cytoplasmic calcium ([Ca2+]c) are linked to dormancy of HSCs. These findings indicate that G0M separates dormant and active adult HSCs, which are regulated by Cdk4/6 and [Ca2+]c. This G0M mouse line represents a useful resource for investigating physiologically important stem cell subpopulations.Entities:
Keywords: CDK; G(0) phase; HSC; calcium; cell cycle; dormancy; hematopoietic stem cell; p27
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Year: 2019 PMID: 31851939 DOI: 10.1016/j.celrep.2019.11.061
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423