Development of specific collagen scaffolds to support the osteogenic and chondrogenic differentiation of human bone marrow stromal cells

被引:116
作者
Dawson, Jonathan I. [1 ]
Wahl, Denys A. [2 ]
Lanham, Stuart A. [1 ]
Kanczler, Janos M. [1 ]
Czernuszka, Jan T. [2 ]
Oreffo, Richard O. C. [1 ]
机构
[1] Southampton Gen Hosp, Inst Dev Sci, Southampton SO16 6YD, Hants, England
[2] Univ Oxford, Dept Mat, Oxford OX1 3PH, England
基金
英国生物技术与生命科学研究理事会;
关键词
bone tissue engineering; cartilage tissue engineering; collagen; scaffold; biomimetic material;
D O I
10.1016/j.biomaterials.2008.03.040
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
Type I Collagen matrices of defined porosity, incorporating carbonate substituted hydroxyapatite (HA) crystals, were assessed for their ability to support osteo- and chondrogenic differentiation of human bone marrow stromal cells (HBMSCs). Collagen-HA composite scaffolds supported the osteogenic differentiation of HBMSCs both in vitro and in vivo as demonstrated by histological and micro-CT analyses indicating the extensive penetration of alkaline phosphatase expressing cells and new matrix synthesis with localised areas immunologically positive for osteocalcin. In vivo, extensive new osteoid formation of implant origin was observed in the areas of vasculature. Chondrogenic matrix synthesis was evidenced in the peripheral regions of pure collagen systems by an abundance of Sox9 expressing chondrocytes embedded within a proteoglycan and collagen II rich ECM. The introduction of microchannels to the scaffold architecture was seen to enhance chondrogenesis. Tissue specific gene expression and corresponding matrix synthesis indicate that collagen matrices support the growth and differentiation of HBMSCs and suggest the potential of this platform for understanding the ECM cues necessary for osteogenesis and chondrogenesis. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3105 / 3116
页数:12
相关论文
共 49 条
[1]
PRODUCTION OF A TISSUE-LIKE STRUCTURE BY CONTRACTION OF COLLAGEN LATTICES BY HUMAN-FIBROBLASTS OF DIFFERENT PROLIFERATIVE POTENTIAL INVITRO [J].
BELL, E ;
IVARSSON, B ;
MERRILL, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (03) :1274-1278
[2]
Design of biomimetic habitats for tissue engineering with P-15, a synthetic peptide analogue of collagen [J].
Bhatnagar, RS ;
Qian, JJ ;
Wedrychowska, A ;
Sadeghi, M ;
Wu, YM ;
Smith, N .
TISSUE ENGINEERING, 1999, 5 (01) :53-65
[3]
Stem cells in tissue engineering [J].
Bianco, P ;
Robey, PG .
NATURE, 2001, 414 (6859) :118-121
[4]
Lapine and canine bone marrow stromal cells contain smooth muscle actin and contract a collagen-glycosaminoglycan matrix [J].
Cai, DZ ;
Marty-Roix, R ;
Hsu, HP ;
Spector, M .
TISSUE ENGINEERING, 2001, 7 (06) :829-841
[5]
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]
THE EFFECT OF OXYGEN-TENSION ON PROTEOGLYCAN SYNTHESIS AND AGGREGATION IN MAMMALIAN GROWTH PLATE CHONDROCYTES [J].
CLARK, CC ;
TOLIN, BS ;
BRIGHTON, CT .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (04) :477-484
[7]
Transduction - Integrin signaling [J].
Giancotti, FG ;
Ruoslahti, E .
SCIENCE, 1999, 285 (5430) :1028-1032
[8]
Hall BK, 1995, INT J DEV BIOL, V39, P881
[9]
Porous scaffold design for tissue engineering [J].
Hollister, SJ .
NATURE MATERIALS, 2005, 4 (07) :518-524
[10]
Injectable scaffolds for tissue regeneration [J].
Hou, QP ;
De Bank, PA ;
Shakesheff, KM .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (13) :1915-1923