Effects of RGD nanospacing on chondrogenic differentiation of mesenchymal stem cells

被引:35
作者
Li, Zhenhua [1 ]
Cao, Bin [1 ]
Wang, Xuan [1 ]
Ye, Kai [1 ]
Li, Shiyu [1 ]
Ding, Jiandong [1 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Polymers & Polymer Composi, State Key Lab Mol Engn Polymers, Dept Macromol Sci,Adv Mat Lab, Shanghai 200433, Peoples R China
关键词
DEPENDENT PROTEIN-KINASE; LIGAND DENSITY; ASPECT RATIOS; IN-VITRO; ADHESION; P38; HYDROGEL; DRUG; IMPACT; MICROPATTERNS;
D O I
10.1039/c5tb00455a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Modification of material surfaces by an arginine-glycine-aspartate (RGD) peptide, a ligand of transmembrane integrin, can regulate cell adhesion and other events in tissue engineering and regenerative medicine. While both RGD effects and chondrogenesis are very important and have been much reported, the studies on the influence of the spatial arrangement of RGD ligands on chondrogenic differentiation are rather limited. Herein, we examined the effects of RGD nanospacing on in vitro two-dimensional chondrogenic differentiation of mesenchymal stem cells (MSCs) for the first time. Using a unique nanolithography technology, hexagonal RGD nanopatterns were generated on nonfouling poly(ethylene glycol) (PEG) hydrogels. Two nanospacings (63 and 161 nm) were achieved, with one below and the other above the critical nanospacing. After one-day incubation and nine-day chondrogenic induction, expressions of collagen II proteins and chondrocyte-specific genes (SOX9, aggrecan and collagen II) were detected. The statistics illustrated that the large nanospacing led to a less spreading area and a higher chondrogenic differentiation extent. Further tests by the addition of an inhibitor SB203580 confirmed the positive regulation of the p38 phospho-relay cascade on the chondrogenic induction in this model system.
引用
收藏
页码:5197 / 5209
页数:13
相关论文
共 64 条
[1]   The differential effect of scaffold composition and architecture on chondrocyte response to mechanical stimulation [J].
Appelman, Taly P. ;
Mizrahi, Joseph ;
Elisseeff, Jennifer H. ;
Seliktar, Dror .
BIOMATERIALS, 2009, 30 (04) :518-525
[2]   Activation of integrin function by nanopatterned adhesive interfaces [J].
Arnold, M ;
Cavalcanti-Adam, EA ;
Glass, R ;
Blümmel, J ;
Eck, W ;
Kantlehner, M ;
Kessler, H ;
Spatz, JP .
CHEMPHYSCHEM, 2004, 5 (03) :383-388
[3]   Induction of cell polarization and migration by a gradient of nanoscale variations in adhesive ligand spacing [J].
Arnold, Marco ;
Hirschfeld-Warneken, Vera C. ;
Lohmueller, Theobald ;
Heil, Patrick ;
Bluemmel, Jacques ;
Cavalcanti-Adam, Elisabetta A. ;
Lopez-Garcia, Monica ;
Walther, Paul ;
Kessler, Horst ;
Geiger, Benjamin ;
Spatz, Joachim P. .
NANO LETTERS, 2008, 8 (07) :2063-2069
[4]   Chondrocyte phenotypes on different extracellular matrix monolayers [J].
Brodkin, KR ;
García, AJ ;
Levenston, ME .
BIOMATERIALS, 2004, 25 (28) :5929-5938
[5]   Effects of spreading areas and aspect ratios of single cells on dedifferentiation of chondrocytes [J].
Cao, Bin ;
Peng, Rong ;
Li, Zhenhua ;
Ding, Jiandong .
BIOMATERIALS, 2014, 35 (25) :6871-6881
[6]   An injectable hydrogel formed by in situ cross-linking of glycol chitosan and multi-benzaldehyde functionalized PEG analogues for cartilage tissue engineering [J].
Cao, Luping ;
Cao, Bin ;
Lu, Chengjiao ;
Wang, Guowei ;
Yu, Lin ;
Ding, Jiandong .
JOURNAL OF MATERIALS CHEMISTRY B, 2015, 3 (07) :1268-1280
[7]   Vinculin Regulates the Recruitment and Release of Core Focal Adhesion Proteins in a Force-Dependent Manner [J].
Carisey, Alex ;
Tsang, Ricky ;
Greiner, Alexandra M. ;
Nijenhuis, Nadja ;
Heath, Nikki ;
Nazgiewicz, Alicja ;
Kemkemer, Ralf ;
Derby, Brian ;
Spatz, Joachim ;
Ballestrem, Christoph .
CURRENT BIOLOGY, 2013, 23 (04) :271-281
[8]   Enhancement of the fraction of the active form of an antitumor drug topotecan via an injectable hydrogel [J].
Chang, Guangtao ;
Ci, Tianyuan ;
Yu, Lin ;
Ding, Jiandong .
JOURNAL OF CONTROLLED RELEASE, 2011, 156 (01) :21-27
[9]  
Chen GP, 2002, MACROMOL BIOSCI, V2, P67, DOI 10.1002/1616-5195(20020201)2:2<67::AID-MABI67>3.3.CO
[10]  
2-6