Bioresponsive phosphoester hydrogels for bone tissue engineering

被引:138
作者
Wang, DA [1 ]
Williams, CG [1 ]
Yang, F [1 ]
Cher, N [1 ]
Lee, H [1 ]
Elisseeff, JH [1 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
来源
TISSUE ENGINEERING | 2005年 / 11卷 / 1-2期
关键词
D O I
10.1089/ten.2005.11.201
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Bioresponsive and intelligent biomaterials are a vehicle for manipulating cell function to promote tissue development and/or tissue engineering. A photopolymerized hydrogel based on a phosphoester - poly( ethylene glycol) polymer (PhosPEG) was synthesized for application to marrow-derived mesenchymal stem cell ( MSC) encapsulation and tissue engineering of bone. The phosphor-containing hydrogels were hydrolytically degradable and the rate of degradation increased in the presence of a bone-derived enzyme, alkaline phosphatase. Gene expression and protein analysis of encapsulated MSCs demonstrated that PhosPEG - PEG cogels containing an intermediate concentration of phosphorus promoted the gene expression of bone-specific markers including type I collagen, alkaline phosphatase, and osteonectin, without the addition of growth factors or other biological agents, compared with pure poly( ethylene glycol)- based gels. Secretion of alkaline phosphatase, osteocalcin, and osteonectin protein was also increased in the PhosPEG cogels. Mineralization of gels increased in the presence of phosphorus in both cellular and acellular constructs compared with PEG gels. In summary, phosphate-PEG-derived hydrogels increase gene expression of bone-specific markers, secretion of bone-related matrix, and mineralization and may have a potential impact on bone-engineering therapies.
引用
收藏
页码:201 / 213
页数:13
相关论文
共 32 条
[11]  
GUNDBERG CM, 1984, METHOD ENZYMOL, V107, P516
[12]   Biologically engineered protein-graft-poly(ethylene glycol) hydrogels:: A cell adhesive and plasm in-degradable biosynthetic material for tissue repair [J].
Halstenberg, S ;
Panitch, A ;
Rizzi, S ;
Hall, H ;
Hubbell, JA .
BIOMACROMOLECULES, 2002, 3 (04) :710-723
[13]   DIRECT IDENTIFICATION OF CALCIUM-BINDING AMINO-ACID, GAMMA-CARBOXYGLUTAMATE, IN MINERALIZED TISSUE [J].
HAUSCHKA, PV ;
LIAN, JB ;
GALLOP, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (10) :3925-3929
[14]   MOLECULAR-WEIGHT DEPENDENCE OF CALCIFICATION OF POLYETHYLENE-GLYCOL HYDROGELS [J].
HOSSAINY, SFA ;
HUBBELL, JA .
BIOMATERIALS, 1994, 15 (11) :921-925
[15]   FLUOROMETRIC ASSAY OF DNA IN CARTILAGE EXPLANTS USING HOECHST-33258 [J].
KIM, YJ ;
SAH, RLY ;
DOONG, JYH ;
GRODZINSKY, AJ .
ANALYTICAL BIOCHEMISTRY, 1988, 174 (01) :168-176
[16]   TISSUE ENGINEERING [J].
LANGER, R ;
VACANTI, JP .
SCIENCE, 1993, 260 (5110) :920-926
[17]   Bone morphogenetic protein-2 restores mineralization in glucocorticoid-inhibited MC3T3-E1 osteoblast cultures [J].
Luppen, CA ;
Smith, E ;
Spevak, L ;
Boskey, AL ;
Frenkel, B .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (07) :1186-1197
[18]   Bioinspired growth of crystalline carbonate apatite on biodegradable polymer substrata [J].
Murphy, WL ;
Mooney, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (09) :1910-1917
[19]  
Peter SJ, 1998, J CELL BIOCHEM, V71, P55, DOI 10.1002/(SICI)1097-4644(19981001)71:1<55::AID-JCB6>3.0.CO
[20]  
2-0