Human bone marrow stromal cells: In vitro expansion and differentiation for bone engineering

被引:118
作者
Ciapetti, G.
Ambrosio, L.
Marletta, G.
Baldini, N.
Giunti, A.
机构
[1] Univ Bologna, Ist Ortoped Rizzoli, Lab Pathophysiol Orthopaed Implants, I-40136 Bologna, Italy
[2] Univ Naples Federico II, Inst Composite & Biomed Mat, IMCB, CNR, I-80125 Naples, Italy
[3] Univ Naples Federico II, Interdisciplinary Res Ctr Biomat, I-80125 Naples, Italy
[4] Univ Catania, Dept Chem Sci, Lab Mol Surfaces & Nanotechnol, I-95125 Catania, Italy
关键词
mesenchymal stem cells; bone marrow; bone tissue engineering; bone regeneration; osteoblast; in vitro test;
D O I
10.1016/j.biomaterials.2006.08.025
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Stromal cells from marrow hold a great promise for bone regeneration. Even if they are already being exploited in many clinical settings, the biological basis for the source and maintenance of their proliferation/differentiation potential after in vitro isolation and expansion needs further investigation. Most studies on osteogenic differentiation of marrow stromal cells (MSC) have been performed using bone marrow from the iliac crest. In this study, MSC were derived from spare femoral bone marrow obtained during hip replacement surgery from 20 adult donors. After in vitro isolation the cells were grown in osteogenic medium, and their proliferation and differentiation analysed during in vitro expansion. We found that MSC isolated from the femur of adult patients consistently maintain an osteogenic potential. Using biochemical signals, these cells turn to fully differentiated osteoblasts with a predictable set of molecular and phenotypic events of in vitro bone deposition. When seeded on polycaprolactone-based scaffold or surfaces, the proliferation and mineralization of femur-derived MSC were modulated by the surface chemistry/topography. Despite remarkable differences between individual colony-forming ability, alkaline phosphatase production, and mineralization ability, these cells are a potential source for bone engineering, either by direct autologous reimplantation or by ex vivo expansion and reimplantation combined to a proper scaffold. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6150 / 6160
页数:11
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