Formation of a chondro-osseous rudiment in micromass cultures of human bone-marrow stromal cells

A Muraglia, A Corsi, M Riminucci… - Journal of cell …, 2003 - journals.biologists.com
A Muraglia, A Corsi, M Riminucci, M Mastrogiacomo, R Cancedda, P Bianco, R Quarto
Journal of cell science, 2003journals.biologists.com
Bone-marrow stromal cells can differentiate into multiple mesenchymal lineages including
cartilage and bone. When these cells are seeded in high-densitypellet culture', they undergo
chondrogenesis and form a tissue that is morphologically and biochemically defined as
cartilage. Here, we show that dual chondro-osteogenic differentiation can be obtained in the
same micromass culture of human bone-marrow stromal cells. Human bone-marrow stromal
cells were pellet cultured for 4 weeks in chondro-inductive medium. Cartilagebeads' …
Bone-marrow stromal cells can differentiate into multiple mesenchymal lineages including cartilage and bone. When these cells are seeded in high-density `pellet culture', they undergo chondrogenesis and form a tissue that is morphologically and biochemically defined as cartilage. Here, we show that dual chondro-osteogenic differentiation can be obtained in the same micromass culture of human bone-marrow stromal cells. Human bone-marrow stromal cells were pellet cultured for 4 weeks in chondro-inductive medium. Cartilage `beads' resulting from the micromass culture were then subcultured for further 1-3 weeks in osteo-inductive medium. This resulted in the formation of a distinct mineralized bony collar around hyaline cartilage. During the chondrogenesis phase, type I collagen and bone sialoprotein were produced in the outer portion of the cartilage bead, which, upon subsequent exposure to β-glycerophosphate, mineralized and accumulated extracellular bone sialoprotein and osteocalcin. Our modification of the pellet culture system results in the formation of a chondro-osseous `organoid' structurally reminiscent of pre-invasion endochondral rudiments, in which a bony collar forms around hyaline cartilage. The transition from a cell culture to an organ culture dimension featured by our system provides a suitable model for the dissection of molecular determinants of endochondral bone formation, which unfolds in a precisely defined spatial and temporal frame
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