TY - JOUR
T1 - Osteoprogenitor Cells from Bone Marrow and Cortical Bone
T2 - Understanding How the Environment Affects Their Fate
AU - Corradetti, Bruna
AU - Taraballi, Francesca
AU - Powell, Sebastian
AU - Sung, David
AU - Minardi, Silvia
AU - Ferrari, Mauro
AU - Weiner, Bradley K.
AU - Tasciotti, Ennio
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Bone is a dynamic organ where skeletal progenitors and hematopoietic cells share and compete for space. Presumptive mesenchymal stem cells (MSC) have been identified and harvested from the bone marrow (BM-MSC) and cortical bone fragments (CBF-MSC). In this study, we demonstrate that despite the cells sharing a common ancestor, the differences in the structural properties of the resident tissues affect cell behavior and prime them to react differently to stimuli. Similarly to the bone marrow, the cortical portion of the bone contains a unique subset of cells that stains positively for the common MSC-associated markers. These cells display different multipotent differentiation capability, clonogenic expansion, and immunosuppressive potential. In particular, when compared with BM-MSC, CBF-MSC are bigger in size, show a lower proliferation rate at early passages, have a greater commitment toward the osteogenic lineage, constitutively produce nitric oxide as a mediator for bone remodeling, and more readily respond to proinflammatory cytokines. Our data suggest that the effect of the tissue's microenvironment makes the CBF-MSC a superior candidate in the development of new strategies for bone repair.
AB - Bone is a dynamic organ where skeletal progenitors and hematopoietic cells share and compete for space. Presumptive mesenchymal stem cells (MSC) have been identified and harvested from the bone marrow (BM-MSC) and cortical bone fragments (CBF-MSC). In this study, we demonstrate that despite the cells sharing a common ancestor, the differences in the structural properties of the resident tissues affect cell behavior and prime them to react differently to stimuli. Similarly to the bone marrow, the cortical portion of the bone contains a unique subset of cells that stains positively for the common MSC-associated markers. These cells display different multipotent differentiation capability, clonogenic expansion, and immunosuppressive potential. In particular, when compared with BM-MSC, CBF-MSC are bigger in size, show a lower proliferation rate at early passages, have a greater commitment toward the osteogenic lineage, constitutively produce nitric oxide as a mediator for bone remodeling, and more readily respond to proinflammatory cytokines. Our data suggest that the effect of the tissue's microenvironment makes the CBF-MSC a superior candidate in the development of new strategies for bone repair.
UR - http://www.scopus.com/inward/record.url?scp=84930793705&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84930793705&partnerID=8YFLogxK
U2 - 10.1089/scd.2014.0351
DO - 10.1089/scd.2014.0351
M3 - Article
C2 - 25517215
AN - SCOPUS:84930793705
SN - 1547-3287
VL - 24
SP - 1112
EP - 1123
JO - Stem Cells and Development
JF - Stem Cells and Development
IS - 9
ER -