Osteogenic induction of human bone marrow-derived mesenchymal progenitor cells in novel synthetic polymer-hydrogel matrices


Autoria(s): Endres, Michaela; Hutmacher, Dietmar; Salgado, A.J.; Kaps, Christian; Ringe, J.; Reis, Rui; Sittinger, Michael; Brandwood, Arthur; Schantz, Jan-Thorsten
Data(s)

2003

Resumo

The aim of this project was to investigate the in vitro osteogenic potential of human mesenchymal progenitor cells in novel matrix architectures built by means of a three-dimensional bioresorbable synthetic framework in combination with a hydrogel. Human mesenchymal progenitor cells (hMPCs) were isolated from a human bone marrow aspirate by gradient centrifugation. Before in vitro engineering of scaffold-hMPC constructs, the adipogenic and osteogenic differentiation potential was demonstrated by staining of neutral lipids and induction of bone-specific proteins, respectively. After expansion in monolayer cultures, the cells were enzymatically detached and then seeded in combination with a hydrogel into polycaprolactone (PCL) and polycaprolactone-hydroxyapatite (PCL-HA) frameworks. This scaffold design concept is characterized by novel matrix architecture, good mechanical properties, and slow degradation kinetics of the framework and a biomimetic milieu for cell delivery and proliferation. To induce osteogenic differentiation, the specimens were cultured in an osteogenic cell culture medium and were maintained in vitro for 6 weeks. Cellular distribution and viability within three-dimensional hMPC bone grafts were documented by scanning electron microscopy, cell metabolism assays, and confocal laser microscopy. Secretion of the osteogenic marker molecules type I procollagen and osteocalcin was analyzed by semiquantitative immunocytochemistry assays. Alkaline phosphatase activity was visualized by p-nitrophenyl phosphate substrate reaction. During osteogenic stimulation, hMPCs proliferated toward and onto the PCL and PCL-HA scaffold surfaces and metabolic activity increased, reaching a plateau by day 15. The temporal pattern of bone-related marker molecules produced by in vitro tissue-engineered scaffold-cell constructs revealed that hMPCs differentiated better within the biomimetic matrix architecture along the osteogenic lineage.

Formato

application/pdf

Identificador

http://eprints.qut.edu.au/38073/

Publicador

Mary Ann Liebert, Inc.

Relação

http://eprints.qut.edu.au/38073/1/Hutmacher.pdf

DOI:10.1089/107632703768247386

Endres, Michaela, Hutmacher, Dietmar, Salgado, A.J., Kaps, Christian, Ringe, J., Reis, Rui, Sittinger, Michael, Brandwood, Arthur, & Schantz, Jan-Thorsten (2003) Osteogenic induction of human bone marrow-derived mesenchymal progenitor cells in novel synthetic polymer-hydrogel matrices. Tissue Engineering Part A: Tissue Engineering, 9(4), pp. 689-702.

Fonte

Faculty of Built Environment and Engineering; School of Engineering Systems

Palavras-Chave #060100 BIOCHEMISTRY AND CELL BIOLOGY #069900 OTHER BIOLOGICAL SCIENCES #090300 BIOMEDICAL ENGINEERING #biomedical engineering
Tipo

Journal Article