The osteogenic differentiation of adult bone marrow and perinatal umbilical mesenchymal stem cells and matrix remodelling in three-dimensional collagen scaffolds

被引:173
作者
Schneider, Rebekka K. [1 ]
Puellen, Andrea [1 ]
Kramann, Rafael [2 ]
Raupach, Kerstin [1 ]
Bornemann, Joerg [3 ]
Knuechel, Ruth [1 ]
Perez-Bouza, Alberto [1 ]
Neuss, Sabine [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Pathol, Univ Hosp, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Univ Hosp, Div Nephrol & Clin Immunol, D-52074 Aachen, Germany
[3] Rhein Westfal TH Aachen, Univ Hosp, Electron Microscop Facil, D-52074 Aachen, Germany
关键词
Human mesenchymal stem cells; Bone tissue engineering; Collagen scaffold; Matrix remodelling; Extracellular matrix; Metalloproteinases; HEMATOPOIETIC PROGENITOR CELLS; STROMAL CELLS; IN-VITRO; CORD; EXPRESSION; THERAPY; METALLOPROTEINASES; TRANSPLANTATION; HUCPVCS; BIOLOGY;
D O I
10.1016/j.biomaterials.2009.09.059
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Adult human mesenchymal stem cells from bone marrow (BM-MSC) represent a promising source for skeletal regeneration. Perinatal MSC from Wharton's Jelly of the umbilical cord (UC-MSC) are expected to possess enhanced differentiation capacities due to partial expression of pluripotency markers. For bone tissue engineering, it is important to analyse in vitro behaviour of stem cell/biomaterial hybrids concerning in vivo integration into injured tissue via migration, matrix remodelling and differentiation. This study compares the cell-mediated remodelling of three-dimensional collagen I/III gels during osteogenic differentiation of both cell types. When activated through collagen contact and subjected to osteogenic differentiation, UC-MSC differ from BM-MSC in expression and synthesis of extracellular matrix (ECM) proteins as shown by histology, immunohistochemistry, Western Blot analysis and realtime-RT-PCR. The biosynthetic activity was accompanied in both cell types by the ultrastructural appearance of hydroxyapatite/calcium crystals and osteogenic gene induction. Following secretion of matrix metalloproteinases (MMP), both MSC types migrated into and colonised the collagenous matrix causing matrix strengthening and contraction. These results indicate that UC-MSC and BM-MSC display all features needed for effective bone fracture healing. The expression of ECM differs in both cell types considerably, suggesting different mechanisms for bone formation and significant impact for bone tissue engineering. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:467 / 480
页数:14
相关论文
共 43 条
[1]   A comparison of human umbilical cord matrix stem cells and temporomandibular joint condylar Chondrocytes for tissue engineering temporomandibular joint condylar cartilage [J].
Bailey, Mark M. ;
Wang, Limin ;
Bode, Claudia J. ;
Mitchell, Kathy E. ;
Detamore, Michael S. .
TISSUE ENGINEERING, 2007, 13 (08) :2003-2010
[2]   Bone marrow stromal stem cells: Nature, biology, and potential applications [J].
Bianco, P ;
Riminucci, M ;
Gronthos, S ;
Robey, PG .
STEM CELLS, 2001, 19 (03) :180-192
[3]   Critical parameters for the isolation of mesenchymal stem cells from umbilical cord blood [J].
Bieback, K ;
Kern, S ;
Klüter, H ;
Eichler, H .
STEM CELLS, 2004, 22 (04) :625-634
[4]  
Bieback Karen, 2007, Curr Stem Cell Res Ther, V2, P310, DOI 10.2174/157488807782793763
[5]   Allograft bone - The influence of processing on safety and performance [J].
Boyce, T ;
Edwards, J ;
Scarborough, N .
ORTHOPEDIC CLINICS OF NORTH AMERICA, 1999, 30 (04) :571-+
[6]  
Bruder SP, 1997, J CELL BIOCHEM, V64, P278, DOI 10.1002/(SICI)1097-4644(199702)64:2<278::AID-JCB11>3.0.CO
[7]  
2-F
[8]  
Campagnoli C, 2002, BJOG-INT J OBSTET GY, V109, P952, DOI 10.1016/S1470-0328(02)02011-6
[9]   Expression of early transcription factors Oct-4, Sox-2 and Nanog by porcine umbilical cord (PUC) matrix cells [J].
Carlin, R ;
Davis, D ;
Weiss, M ;
Schultz, B ;
Troyer, D .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2006, 4 (1)
[10]   Isolation of amniotic stem cell lines with potential for therapy [J].
De Coppi, Paolo ;
Bartsch, Georg, Jr. ;
Siddiqui, M. Minhaj ;
Xu, Tao ;
Santos, Cesar C. ;
Perin, Laura ;
Mostoslavsky, Gustavo ;
Serre, Angeline C. ;
Snyder, Evan Y. ;
Yoo, James J. ;
Furth, Mark E. ;
Soker, Shay ;
Atala, Anthony .
NATURE BIOTECHNOLOGY, 2007, 25 (01) :100-106