TY - JOUR
T1 - Mesenchymal stem cell-organized bone marrow elements
T2 - An alternative hematopoietic progenitor resource
AU - Miura, Yasuo
AU - Gao, Zhigang
AU - Miura, Masako
AU - Seo, Byoung Moo
AU - Sonoyama, Wataru
AU - Chen, Wanjun
AU - Gronthos, Stan
AU - Zhang, Li
AU - Shi, Songtao
PY - 2006
Y1 - 2006
N2 - Bone marrow-derived mesenchymal stem cells (BMMSCs) are multipotent postnatal stem cells that have been used for the treatment of bone defects and graft-versus-host diseases in clinics. In this study, we found that subcutaneously transplanted human BMMSCs are capable of organizing hematopoietic progenitors of recipient origin. These hematopoietic cells expressed multiple lineages of hematopoietic cell associated markers and were able to rescue lethally irradiated mice, with successful engraftment in the recipient, suggesting a potential bone marrow (BM) resource for stem cell therapies. Furthermore, we found that platelet-derived growth factor (PDGF) promotes the formation of BMMSC-generated BM niches through upregulation of β-catenin, implying that the PDGF pathway contributes to the formation of ectopic BM. These results indicate that the BMMSC-organized BM niche system represents a unique hematopoietic progenitor resource possessing potential clinical value.
AB - Bone marrow-derived mesenchymal stem cells (BMMSCs) are multipotent postnatal stem cells that have been used for the treatment of bone defects and graft-versus-host diseases in clinics. In this study, we found that subcutaneously transplanted human BMMSCs are capable of organizing hematopoietic progenitors of recipient origin. These hematopoietic cells expressed multiple lineages of hematopoietic cell associated markers and were able to rescue lethally irradiated mice, with successful engraftment in the recipient, suggesting a potential bone marrow (BM) resource for stem cell therapies. Furthermore, we found that platelet-derived growth factor (PDGF) promotes the formation of BMMSC-generated BM niches through upregulation of β-catenin, implying that the PDGF pathway contributes to the formation of ectopic BM. These results indicate that the BMMSC-organized BM niche system represents a unique hematopoietic progenitor resource possessing potential clinical value.
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U2 - 10.1634/stemcells.2006-0089
DO - 10.1634/stemcells.2006-0089
M3 - Article
C2 - 17071859
AN - SCOPUS:33750571850
SN - 1066-5099
VL - 24
SP - 2428
EP - 2436
JO - Stem Cells
JF - Stem Cells
IS - 11
ER -