Rapid 3D bioprinting of decellularized extracellular matrix with regionally varied mechanical properties and biomimetic microarchitecture

被引:190
作者
Ma, Xuanyi [1 ]
Yu, Claire [2 ]
Wang, Pengrui [3 ]
Xu, Weizhe [1 ]
Wan, Xueyi [4 ]
Lai, Cheuk Sun Edwin [5 ]
Liu, Justin [3 ]
Koroleva-Maharajh, Anna [2 ]
Chen, Shaochen [1 ,2 ,3 ,5 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept NanoEngn, 9500 Gilman Dr Mail Code 0448, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Mat Sci & Engn Program, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Chem Engn Program, La Jolla, CA 92093 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
3D bioprinting; Decellularized extracellular matrix; Cancer invasion; Liver fibrosis; Tissue engineering; HEPATOCELLULAR-CARCINOMA; LIVER STIFFNESS; TUMOR; CULTURE; METALLOPROTEINASES; METASTASIS; CELLS;
D O I
10.1016/j.biomaterials.2018.09.026
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hepatocellular carcinoma (HCC), as the fifth most common malignant cancer, develops and progresses mostly in a cirrhotic liver where stiff nodules are separated by fibrous bands. Scaffolds that can provide a 3D cirrhotic mechanical environment with complex native composition and biomimetic architecture are necessary for the development of better predictive tissue models. Here, we developed photocrosslinkable liver decellularized extracellular matrix (dECM) and a rapid light-based 3D bioprinting process to pattern liver dECM with tailorable mechanical properties to serve as a platform for HCC progression study. 3D bioprinted liver dECM scaffolds were able to stably recapitulate the clinically relevant mechanical properties of cirrhotic liver tissue. When encapsulated in dECM scaffolds with cirrhotic stiffness, HepG2 cells demonstrated reduced growth along with an upregulation of invasion markers compared to healthy controls. Moreover, an engineered cancer tissue platform possessing tissue-scale organization and distinct regional stiffness enabled the visualization of HepG2 stromal invasion from the nodule with cirrhotic stiffness. This work demonstrates a significant advancement in rapid 3D patterning of complex ECM biomaterials with biomimetic architecture and tunable mechanical properties for in vitro disease modeling.
引用
收藏
页码:310 / 321
页数:12
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