Varying PEG density to control stress relaxation in alginate-PEG hydrogels for 3D cell culture studies

被引:182
|
作者
Nam, Sungmin [1 ]
Stowers, Ryan [1 ]
Lou, Junzhe [2 ,3 ]
Xia, Yan [2 ]
Chaudhuri, Ovijit [1 ]
机构
[1] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Hydrogels; 3D cell culture; Viscoelasticity; Stress relaxation; alginate and PEG; ADAPTABLE NETWORKS; MATRIX; BIOMATERIALS; FORCES; SOFT;
D O I
10.1016/j.biomaterials.2019.02.004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hydrogels are commonly used as artificial extracellular matrices for 3D cell culture and for tissue engineering. Viscoelastic hydrogels with tunable stress relaxation have recently been developed, and stress relaxation in the hydrogels has been found to play a key role in regulating cell behaviors such as differentiation, spreading, and proliferation. Here we report a simple but precise materials approach to tuning stress relaxation of alginate hydrogels with polyethylene glycol (PEG) covalently grafted onto the alginate. Hydrogel relaxation was modulated independent of the initial elastic modulus by varying molecular weight and concentration of PEG along with calcium crosslinking of the alginate. Increased concentration and molecular weight of the PEG resulted in faster stress relaxation, a higher loss modulus, and increased creep. Interestingly, we found that stress relaxation of the hydrogels is determined by the total mass amount of PEG in the hydrogel, and not the molecular weight or concentration of PEG chains alone. We then evaluated the utility of these hydrogels for 3D cell culture. Faster relaxation in RGD-coupled alginate-PEG hydrogels led to increased spreading and proliferation of fibroblasts, and enhanced osteogenic differentiation of mesenchymal stem cells (MSCs). Thus, this work establishes a new materials approach to tuning stress relaxation in alginate hydrogels for 3D cell culture.
引用
收藏
页码:15 / 24
页数:10
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