Perfusion and cyclic compression of mesenchymal cell-loaded and clinically applicable osteochondral grafts

被引:11
作者
Haasper, Carl [1 ]
Colditz, Michael [1 ]
Budde, Stefan [1 ]
Hesse, Eric [1 ,4 ]
Tschernig, Thomas [3 ]
Frink, Michael [1 ]
Krettek, Christian [1 ]
Hurschler, Christof [2 ]
Jagodzinski, Michael [1 ]
机构
[1] Hannover Med Sch MHH, Trauma Dept, D-30625 Hannover, Germany
[2] Hannover Med Sch MHH, Lab Biomech & Expt Orthopaed, Dept Orthopaed, D-30625 Hannover, Germany
[3] Hannover Med Sch MHH, Inst Funct & Appl Anat, D-30625 Hannover, Germany
[4] Harvard Univ, Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA 02115 USA
关键词
Cartilage; Bone; Stromal cells; Osteochondral lesion; Bioreactor; Joint disease; MARROW STROMAL CELLS; IN-VITRO; STEM-CELLS; OSTEOGENIC DIFFERENTIATION; PROGENITOR CELLS; TISSUE; BONE; CARTILAGE; PROLIFERATION; CHONDROGENESIS;
D O I
10.1007/s00167-009-0791-3
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Osteochondral lesions are often seen in orthopedics, but the available treatment strategies are limited in success. Regenerative medicine provides novel concepts for curing them. The purpose of this study was to test the effects of perfusion and cyclic compression on cell differentiation and mechanical properties using a custom-made biomechanoreactor in a recently established system of human bone marrow stromal cells (hBMSC) cultured in a 3-D collagen I-bone hybrid matrix out of commercially available and separately in human-certified products. Seeded hBMSC were viable for 88 +/- A 8.9% during the entire experimental period in the constructs. GAG and DNA levels did not change. Perfusion induced collagen II and cyclic compression increased collagen X expression. Matrix stiffness was significantly increased after 28 days of cyclic compression. Cyclic compression of cell-loaded hybrid constructs enhanced chondrocyte differentiation and matrix stiffness. This system is a promising tool with a view to a later clinical application.
引用
收藏
页码:1384 / 1392
页数:9
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