Resveratrol-conjugated poly-ε-caprolactone facilitates in vitro mineralization and in vivo bone regeneration

被引:69
作者
Li, Yan [1 ]
Danmark, Staffan [2 ]
Edlund, Ulrica [2 ]
Finne-Wistrand, Anna [2 ]
He, Xu [1 ]
Norgard, Maria
Blomen, Eva [3 ]
Hultenby, Kjell [3 ]
Andersson, Goran [4 ]
Lindgren, Urban [1 ]
机构
[1] Karolinska Inst, Div Orthoped, Dept Clin Sci Intervent & Technol CLINTEC, Stockholm, Sweden
[2] Royal Inst Technol, Sch Chem Sci & Engn, Stockholm, Sweden
[3] Karolinska Inst, Karolinska Univ Hosp Huddinge, Div Clin Res Ctr, Dept Lab Med, Stockholm, Sweden
[4] Karolinska Inst, Karolinska Univ Hosp Huddinge, Div Pathol, Dept Lab Med, Stockholm, Sweden
关键词
Resveratrol; Biodegradable scaffolds; Bone regeneration; Vapor phase grafting; Tissue engineering; COVALENT FUNCTIONALIZATION; SURFACE FUNCTIONALIZATION; POROUS SCAFFOLDS; PECTINATE BEADS; L-LACTIDE; DIFFERENTIATION; COPOLYMERS; DURA; PROLIFERATION; FORMULATION;
D O I
10.1016/j.actbio.2010.09.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Incorporation of osteoinductive factors in a suitable scaffold is considered a promising strategy for generating osteogenic biomaterials. Resveratrol is a polyphenol found in parts of certain plants, including nuts, berries and grapes. It is known to increase DNA synthesis and alkaline phosphatase (ALP) activity in osteoblasts and to prevent femoral bone loss in ovariectomized (OVX) rats. In the present study resveratrol was coupled through a hydrolysable covalent bond with the carboxylic acid groups in porous poly-epsilon-caprolactone (PCL) surface grafted with acrylic acid (AA). The osteogenic effect of this new scaffold was evaluated in mesenchymal cell culture and in the rat calvarial defect model. We found that the incorporation of resveratrol caused increased ALP activity of rat bone marrow stromal cells and enhanced mineralization of the cell-scaffold composites in vitro. After 8 weeks the calvarial defects implanted with resveratrol-conjugated PCL displayed a higher X-ray density than the defects implanted with control PCL. Bone-like structures, positively immunostained for bone sialoprotein, were shown to be more extensively formed in the resveratrol-conjugated PCL These results show that incorporation of resveratrol into the AA-functionalized porous PCL scaffold led to a significant increase in osteogenesis. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 46 条
[1]   Osteoinduction, osteoconduction and osseointegration [J].
Albrektsson, T ;
Johansson, C .
EUROPEAN SPINE JOURNAL, 2001, 10 (Suppl 2) :S96-S101
[2]   Resilient bioresorbable copolymers based on trimethylene carbonate, L-lactide, and 1,5-dioxepan-2-one [J].
Andronova, Natalia ;
Albertsson, Ann-Christine .
BIOMACROMOLECULES, 2006, 7 (05) :1489-1495
[3]   Osteogenic differentiation of dura mater stem cells cultured in vitro on three-dimensional porous scaffolds of poly(ε-caprolactone) fabricated via co-extrusion and gas foaming [J].
Aronin, C. E. Petrie ;
Cooper, J. A., Jr. ;
Sefcik, L. S. ;
Tholpady, S. S. ;
Ogle, R. C. ;
Botchwey, E. A. .
ACTA BIOMATERIALIA, 2008, 4 (05) :1187-1197
[4]   Resveratrol: A review of preclinical studies for human cancer prevention [J].
Athar, Mohammad ;
Back, Jung Ho ;
Tang, Xmwel ;
Kim, Kwang Ho ;
Kopelovich, Levy ;
Bickers, David R. ;
Kim, Arianna L. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 224 (03) :274-283
[5]  
Aubin JE, 1998, J CELL BIOCHEM, P73, DOI 10.1002/(SICI)1097-4644(1998)72:30/31+<73::AID-JCB11>3.0.CO
[6]  
2-L
[7]   Activation of Sirt1 decreases adipocyte formation during osteoblast differentiation of mesenchymal stem cells [J].
Bäckesjö, CM ;
Li, Y ;
Lindgren, U ;
Haldosén, LA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 (07) :993-1002
[8]   Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[9]  
Bavaresco L, 2003, DRUG EXP CLIN RES, V29, P181
[10]   Bone morphogenetic proteins in tissue engineering: the road from laboratory to clinic, part II (BMP delivery) [J].
Bessa, P. C. ;
Casal, M. ;
Reis, R. L. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2008, 2 (2-3) :81-96