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SCA-1 Expression Level Identifies Quiescent Hematopoietic Stem and Progenitor Cells

Blood cell generation depends on continuous cellular output by the sequential hierarchy of hematopoietic stem cell (HSC) and progenitor populations that all contain quiescent and actively cycling cells. Hematopoietic stem and progenitor cells (HSPCs) express the surface molecule Stem cell antigen 1...

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Detalles Bibliográficos
Autores principales: Morcos, Mina N.F., Schoedel, Kristina B., Hoppe, Anja, Behrendt, Rayk, Basak, Onur, Clevers, Hans C., Roers, Axel, Gerbaulet, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469944/
https://www.ncbi.nlm.nih.gov/pubmed/28506535
http://dx.doi.org/10.1016/j.stemcr.2017.04.012
Descripción
Sumario:Blood cell generation depends on continuous cellular output by the sequential hierarchy of hematopoietic stem cell (HSC) and progenitor populations that all contain quiescent and actively cycling cells. Hematopoietic stem and progenitor cells (HSPCs) express the surface molecule Stem cell antigen 1 (SCA-1/LY6A). Using histone 2B-red fluorescent fusion protein label retention and cell-cycle reporter mice, we demonstrate that high SCA-1 expression (SCA-1(hi)) identifies not only quiescent HSCs but quiescent cells on all hierarchical levels within the lineage(−)SCA-1(+)KIT(+) (LSK) population. Each transplanted SCA-1(hi) HSPC population also displayed self-renewal potential superior to that of the respective SCA-1(lo) population. SCA-1 expression is inducible by type I interferon (IFN). We show, however, that quiescence and high self-renewal capacity of cells with brighter SCA-1 expression at steady state were independent of type I IFN signaling. We conclude that SCA-1 expression levels can be used to prospectively isolate functionally heterogeneous HSPC subpopulations.