Enzyme responsive GAG-based natural-synthetic hybrid hydrogel for tunable growth factor delivery and stem cell differentiation

被引:112
作者
Anjum, Fraz [1 ]
Lienemann, Philipp S. [2 ]
Metzger, Stephanie [2 ]
Biernaskie, Jeff [3 ,4 ,5 ]
Kallos, Michael S. [1 ,6 ]
Ehrbar, Martin [2 ]
机构
[1] Univ Calgary, Pharmaceut Prod Res Facil, 2500 Univ Dr, Calgary, AB T2N 1N4, Canada
[2] Univ Zurich, Univ Zurich Hosp, Dept Obstet, Schmelzbergstr 12, CH-8091 Zurich, Switzerland
[3] Univ Calgary, Fac Vet Med, Dept Comparat Biol & Expt Med, 3330 Hosp Dr, Calgary, AB T2N 4N1, Canada
[4] Univ Calgary, Alberta Childrens Hosp, Res Inst, 3330 Hosp Dr, Calgary, AB T2N 4N1, Canada
[5] Univ Calgary, Cumming Sch Med, Dept Surg, 3330 Hosp Dr, Calgary, AB T2N 4N1, Canada
[6] Univ Calgary, Schulich Sch Engn, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
基金
瑞士国家科学基金会;
关键词
Chondroitin sulphate; Hydrogels; Polyethylene glycol; Factor XIII; Matrix metalloproteinase (MMP); CHONDROITIN SULFATE; CHONDROGENIC DIFFERENTIATION; CROSS-LINKING; MECHANICAL-PROPERTIES; PORE-SIZE; NETWORK; MIGRATION; ADHESIVE; MATRICES; BINDING;
D O I
10.1016/j.biomaterials.2016.01.050
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
We describe an enzymatically formed chondroitin sulfate (CS) and poly(ethylene glycol) (PEG) based hybrid hydrogel system, which by tuning the architecture and composition of modular building blocks, allows the application-specific tailoring of growth factor delivery and cellular responses. CS, a negatively charged sulfate-rich glycosaminoglycan of the extracellular matrix (ECM), known for its growth factor binding and stem cell regulatory functions, is used as a starting material for the engineering of this biomimetic materials platform. The functionalization of CS with transglutaminase factor XIII specific substrate sequences is utilized to allow cross-linking of CS with previously described fibrin-mimetic TG-PEG hydrogel precursors. We show that the hydrogel network properties can be tuned by varying the degree of functionalization of CS as well as the ratio and concentrations of PEG and CS precursors. Taking advantage of TG-PEG hydrogel, compatible tagged bio-functional building blocks, including RGD peptides or matrix metalloproteinase sensitive domains, can be incorporated on demand allowing the three-dimensional culture and expansion of human bone marrow mesenchymal stem cells (BM-MSC5). The binding of bone morphogenetic protein-2 (BMP-2) in a CS concentration dependent manner and the BMP-2 release mediated osteogenic differentiation of BM-MSCs indicate the potential of CS-PEG hybrid hydrogels to promote regeneration of bone tissue. Their modular design allows facile incorporation of additional signaling elements, rendering CS-PEG hydrogels a highly flexible platform with potential for multiple biomedical applications. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 117
页数:14
相关论文
共 71 条
[1]
Baldwin A.D., 2012, POLYM CHEM
[2]
A coarse-grained molecular model for glycosaminoglycans: Application to chondroitin, chondroitin sulfate, and hyaluronic acid [J].
Bathe, M ;
Rutledge, GC ;
Grodzinsky, AJ ;
Tidor, B .
BIOPHYSICAL JOURNAL, 2005, 88 (06) :3870-3887
[3]
Chitosan/alginate crosslinked hydrogels: Preparation, characterization and application for cell growth purposes [J].
Baysal, Kemal ;
Aroguz, Ayse Z. ;
Adiguzel, Zelal ;
Baysal, Bahattin M. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2013, 59 :342-348
[4]
Crosstalk between tyrosine kinase receptors, GSK3 and BMP2 signaling during osteoblastic differentiation of human mesenchymal stem cells [J].
Biver, Emmanuel ;
Thouverey, Cyril ;
Magne, David ;
Caverzasio, Joseph .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2014, 382 (01) :120-130
[5]
Hydrogel-based drug delivery systems: Comparison of drug diffusivity and release kinetics [J].
Brandl, Ferdinand ;
Kastner, Fritz ;
Gschwind, Ruth M. ;
Blunk, Torsten ;
Tessmar, Joerg ;
Goepferich, Achim .
JOURNAL OF CONTROLLED RELEASE, 2010, 142 (02) :221-228
[6]
Crosslinking density influences chondrocyte metabolism in dynamically loaded photocrosslinked poly(ethylene glycol) hydrogels [J].
Bryant, SJ ;
Chowdhury, TT ;
Lee, DA ;
Bader, DL ;
Anseth, KS .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (03) :407-417
[7]
CORRELATION BETWEEN MESH SIZE AND EQUILIBRIUM DEGREE OF SWELLING OF POLYMERIC NETWORKS [J].
CANAL, T ;
PEPPAS, NA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1989, 23 (10) :1183-1193
[8]
Oxidized chondroitin sulfate-cross-linked gelatin matrixes: A new class of hydrogels [J].
Dawlee, S ;
Sugandhi, A ;
Balakrishnan, B ;
Labarre, D ;
Jayakrishnan, A .
BIOMACROMOLECULES, 2005, 6 (04) :2040-2048
[9]
Advances in Bioactive Hydrogels to Probe and Direct Cell Fate [J].
DeForest, Cole A. ;
Anseth, Kristi S. .
ANNUAL REVIEW OF CHEMICAL AND BIOMOLECULAR ENGINEERING, VOL 3, 2012, 3 :421-444
[10]
OPTIMAL ESTIMATION OF CELL-MOVEMENT INDEXES FROM THE STATISTICAL-ANALYSIS OF CELL TRACKING DATA [J].
DICKINSON, RB ;
TRANQUILLO, RT .
AICHE JOURNAL, 1993, 39 (12) :1995-2010