Chondrogenesis of cocultures of mesenchymal stem cells and articular chondrocytes in poly(L-lysine)-loaded hydrogels

被引:15
|
作者
Kim, Yu Seon [1 ]
Chien, Athena J. [1 ]
Guo, Jason L. [1 ]
Smith, Brandon T. [1 ]
Watson, Emma [1 ]
Pearce, Hannah A. [1 ]
Koons, Gerry L. [1 ]
Navara, Adam M. [1 ]
Lam, Johnny [1 ,3 ]
Scott, David W. [2 ]
Grande-Allen, K. Jane [1 ]
Mikos, Antonios G. [1 ]
机构
[1] Rice Univ, Dept Bioengn, 6500 Main St, Houston, TX 77030 USA
[2] Rice Univ, Dept Stat, 6100 Main St, Houston, TX 77005 USA
[3] US FDA, Div Cellular & Gene Therapies, Ctr Biol Evaluat & Res, 10,903 New Hampshire Ave, Silver Spring, MD 20993 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Poly(L-lysine); Mesenchymal stem cell; Chondrocyte; Coculture; Chondrogenesis; Hydrogel; Hypertrophy; Cartilage tissue engineering; IN-VITRO CHONDROGENESIS; CHONDROITIN SULFATE; CARTILAGE; DIFFERENTIATION; HYPERTROPHY; STIMULATION;
D O I
10.1016/j.jconrel.2020.09.048
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work investigated the effect of poly(L-lysine) (PLL) molecular weight and concentration on chondrogenesis of cocultures of mesenchymal stem cells (MSCs) and articular chondrocytes (ACs) in PLL-loaded hydrogels. An injectable dual-network hydrogel composed of a poly(N-isopropylacrylamide)-based synthetic thermogelling macromer and a chondroitin sulfate-based biological network was leveraged as a model to deliver PLL and encapsulate the two cell populations. Incorporation of PLL into the hydrogel did not affect the hydrogel's swelling properties and degradation characteristics, nor the viability of encapsulated cells. Coculture groups demonstrated higher type II collagen expression compared to the MSC monoculture group. Expression of hypertrophic phenotype was also limited in the coculture groups. Histological analysis indicated that the ratio of MSCs to ACs was an accurate predictor of the degree of long-term chondrogenesis, while the presence of PLL was shown to have a more substantial short-term effect. Altogether, this study demonstrates that coculturing MSCs with ACs can greatly enhance the chondrogenicity of the overall cell population and offers a platform to further elucidate the short- and long-term effect of polycationic factors on the chondrogenesis of MSC and AC cocultures.
引用
收藏
页码:710 / 721
页数:12
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