Hematopoietic Cells and Osteoblasts Are Derived from a Common Marrow Progenitor after Bone Marrow Transplantation

Bone and bone marrow are closely aligned physiologic compartments, suggesting that these tissues may represent a single functional unit with a common bone marrow progenitor that gives rise to both osteoblasts and hematopoietic cells. Although reports of multilineage engraftment by a single marrow-de...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2004-08, Vol.101 (32), p.11761-11766
Hauptverfasser: Dominici, Massimo, Pritchard, Colin, Garlits, John E., Hofmann, Ted J., Persons, Derek A., Horwitz, Edwin M., Prockop, Darwin J.
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Sprache:eng
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Zusammenfassung:Bone and bone marrow are closely aligned physiologic compartments, suggesting that these tissues may represent a single functional unit with a common bone marrow progenitor that gives rise to both osteoblasts and hematopoietic cells. Although reports of multilineage engraftment by a single marrow-derived stem cell support this idea, more recent evidence has challenged claims of stem cell transdifferentiation and therefore the existence of a multipotent hematopoietic/osteogenic progenitor cell. Using a repopulation assay in mice, we show here that gene-marked, transplantable marrow cells from the plastic-nonadherent population can generate both functional osteoblasts/osteocytes and hematopoietic cells. Fluorescent in situ hybridization for the X and Y chromosomes and karyotype analysis of cultured osteoblasts confirmed the donor origin of these cells and excluded their generation by a fusion process. Molecular analysis demonstrated a common retroviral integration site in clonogenic hematopoietic cells and osteoprogenitors from each of seven animals studied, establishing a shared clonal origin for these ostensibly independent cell types. Our findings indicate that the bone marrow contains a primitive cell able to generate both the hematopoietic and osteocytic lineages. Its isolation and characterization may suggest novel treatments for genetic bone diseases and bone injuries.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0404626101