Assembly of complex cell microenvironments using geometrically docked hydrogel shapes

被引:72
作者
Eng, George [1 ,3 ]
Lee, Benjamin W. [1 ,3 ]
Parsa, Hesam [1 ]
Chin, Curtis D. [1 ]
Schneider, Jesse [1 ]
Linkov, Gary [3 ]
Sia, Samuel K. [1 ]
Vunjak-Novakovic, Gordana [1 ,2 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10032 USA
[2] Columbia Univ, Dept Med, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
microtechnologies; tissue assembly; angiogenesis; modeling; diffusion; MESENCHYMAL STEM-CELLS; BLOOD-VESSEL FORMATION; TISSUE CONSTRUCTS; IN-VITRO; MIGRATION; GROWTH; BIOMATERIALS; FABRICATION; MICROSTRUCTURES; METASTASIS;
D O I
10.1073/pnas.1300569110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Cellular communities in living tissues act in concert to establish intricate microenvironments, with complexity difficult to recapitulate in vitro. We report a method for docking numerous cellularized hydrogel shapes (100-1,000 mu m in size) into hydrogel templates to construct 3D cellular microenvironments. Each shape can be uniquely designed to contain customizable concentrations of cells and molecular species, and can be placed into any spatial configuration, providing extensive compositional and geometric tunability of shape-coded patterns using a highly biocompatible hydrogel material. Using precisely arranged hydrogel shapes, we investigated migratory patterns of human mesenchymal stem cells and endothelial cells. We then developed a finite element gradient model predicting chemotactic directions of cell migration in micropatterned cocultures that were validated by tracking similar to 2,500 individual cell trajectories. This simple yet robust hydrogel platform provides a comprehensive approach to the assembly of 3D cell environments.
引用
收藏
页码:4551 / 4556
页数:6
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