Human umbilical cord blood-borne fibroblasts contain marrow niche precursors that form a bone/marrow organoid in vivo

Human umbilical cord blood (CB) has attracted much attention as a reservoir for functional hematopoietic stem and progenitor cells, and, recently, as a source of blood-borne fibroblasts (CB-BFs). Previously, we demonstrated that bone marrow stromal cell (BMSC) and CB-BF pellet cultures make cartilag...

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Veröffentlicht in:Development (Cambridge) 2017-03, Vol.144 (6), p.1035-1044
Hauptverfasser: Pievani, Alice, Sacchetti, Benedetto, Corsi, Alessandro, Rambaldi, Benedetta, Donsante, Samantha, Scagliotti, Valeria, Vergani, Patrizia, Remoli, Cristina, Biondi, Andrea, Robey, Pamela G, Riminucci, Mara, Serafini, Marta
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Sprache:eng
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Zusammenfassung:Human umbilical cord blood (CB) has attracted much attention as a reservoir for functional hematopoietic stem and progenitor cells, and, recently, as a source of blood-borne fibroblasts (CB-BFs). Previously, we demonstrated that bone marrow stromal cell (BMSC) and CB-BF pellet cultures make cartilage Furthermore, upon transplantation, BMSC pellets remodelled into miniature bone/marrow organoids. Using this model, we asked whether CB-BF populations that express characteristics of the hematopoietic stem cell (HSC) niche contain precursors that reform the niche. CB ossicles were regularly observed upon transplantation. Compared with BM ossicles, CB ossicles showed a predominance of red marrow over yellow marrow, as demonstrated by histomorphological analyses and the number of hematopoietic cells isolated within ossicles. Marrow cavities from CB and BM ossicles included donor-derived CD146-expressing osteoprogenitors and host-derived mature hematopoietic cells, clonogenic lineage-committed progenitors and HSCs. Furthermore, human CD34 cells transplanted into ossicle-bearing mice engrafted and maintained human HSCs in the niche. Our data indicate that CB-BFs are able to recapitulate the conditions by which the bone marrow microenvironment is formed and establish complete HSC niches, which are functionally supportive of hematopoietic tissue.
ISSN:0950-1991
1477-9129
DOI:10.1242/dev.142836