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Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche

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  • Xingbin Hu

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope
    Xijing Hospital, Fourth Military Medical University)

  • Mayra Garcia

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope)

  • Lihong Weng

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope)

  • Xiaoman Jung

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope)

  • Jodi L. Murakami

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope
    Irell & Manella Graduate School of Biological Sciences, City of Hope)

  • Bijender Kumar

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope)

  • Charles D. Warden

    (Bioinformatics Core, Beckman Research Institute of City of Hope)

  • Ivan Todorov

    (Beckman Research Institute of City of Hope)

  • Ching-Cheng Chen

    (Divison of Hematopoietic Stem Cell and Leukemia Research, Gehr Family Center for Leukemia Research, Beckman Research Institute of City of Hope
    Irell & Manella Graduate School of Biological Sciences, City of Hope)

Abstract

Microenvironment cues received by haematopoietic stem cells (HSC) are important in regulating the choice between self-renewal and differentiation. On the basis of the differential expression of cell-surface markers, here we identify a mesenchymal stromal progenitor hierarchy, where CD45−Ter119−CD31−CD166−CD146−Sca1+(Sca1+) progenitors give rise to CD45−Ter119−CD31−CD166−CD146+(CD146+) intermediate and CD45−Ter119−CD31−CD166+CD146−(CD166+) mature osteo-progenitors. All three progenitors preserve HSC long-term multi-lineage reconstitution capability in vitro; however, their in vivo fates are different. Post-transplantation, CD146+ and CD166+ progenitors form bone only. While Sca1+ progenitors produce CD146+, CD166+ progenitors, osteocytes and CXCL12-producing stromal cells. Only Sca1+ progenitors are capable of homing back to the marrow post-intravenous infusion. Ablation of Sca1+ progenitors results in a decrease of all three progenitor populations as well as haematopoietic stem/progenitor cells. Moreover, suppressing production of KIT-ligand in Sca1+ progenitors inhibits their ability to support HSCs. Our results indicate that Sca1+ progenitors, through the generation of both osteogenic and stromal cells, provide a supportive environment for hematopoiesis.

Suggested Citation

  • Xingbin Hu & Mayra Garcia & Lihong Weng & Xiaoman Jung & Jodi L. Murakami & Bijender Kumar & Charles D. Warden & Ivan Todorov & Ching-Cheng Chen, 2016. "Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche," Nature Communications, Nature, vol. 7(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13095
    DOI: 10.1038/ncomms13095
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