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

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(−)C...

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Autores principales: Hu, Xingbin, Garcia, Mayra, Weng, Lihong, Jung, Xiaoman, Murakami, Jodi L., Kumar, Bijender, Warden, Charles D., Todorov, Ivan, Chen, Ching-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062560/
https://www.ncbi.nlm.nih.gov/pubmed/27721421
http://dx.doi.org/10.1038/ncomms13095
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author Hu, Xingbin
Garcia, Mayra
Weng, Lihong
Jung, Xiaoman
Murakami, Jodi L.
Kumar, Bijender
Warden, Charles D.
Todorov, Ivan
Chen, Ching-Cheng
author_facet Hu, Xingbin
Garcia, Mayra
Weng, Lihong
Jung, Xiaoman
Murakami, Jodi L.
Kumar, Bijender
Warden, Charles D.
Todorov, Ivan
Chen, Ching-Cheng
author_sort Hu, Xingbin
collection PubMed
description 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.
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spelling pubmed-50625602016-10-27 Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche Hu, Xingbin Garcia, Mayra Weng, Lihong Jung, Xiaoman Murakami, Jodi L. Kumar, Bijender Warden, Charles D. Todorov, Ivan Chen, Ching-Cheng Nat Commun Article 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. Nature Publishing Group 2016-10-10 /pmc/articles/PMC5062560/ /pubmed/27721421 http://dx.doi.org/10.1038/ncomms13095 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hu, Xingbin
Garcia, Mayra
Weng, Lihong
Jung, Xiaoman
Murakami, Jodi L.
Kumar, Bijender
Warden, Charles D.
Todorov, Ivan
Chen, Ching-Cheng
Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title_full Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title_fullStr Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title_full_unstemmed Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title_short Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
title_sort identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062560/
https://www.ncbi.nlm.nih.gov/pubmed/27721421
http://dx.doi.org/10.1038/ncomms13095
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