Microcavity substrates casted from self-assembled microsphere monolayers for spheroid cell culture

被引:12
作者
Shen, Keyue [1 ,2 ]
Lee, Jungwoo [1 ,2 ]
Yarmush, Martin L. [1 ,2 ,3 ]
Parekkadan, Biju [1 ,2 ,4 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Engn Med & Surg Serv,Dept Surg, Boston, MA 02114 USA
[2] Shriners Hosp Children, Boston, MA 02114 USA
[3] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
[4] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
基金
美国国家卫生研究院;
关键词
Self-Assembly; Multicellular Spheroid; Microbead-Microcavity; 3-Dimensional Cell Culture; Drug Screening; MULTICELLULAR TUMOR SPHEROIDS; COLLOIDAL PARTICLES; ARRAYS; TISSUE; SIZE; FORCES; CHIP; BIOLUMINESCENCE; MICROWELLS; GENERATION;
D O I
10.1007/s10544-014-9863-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Multicellular spheroids are an important 3-dimensional cell culture model that reflects many key aspects of in vivo microenvironments. This paper presents a scalable, self-assembly based approach for fabricating microcavity substrates for multicellular spheroid cell culture. Hydrophobic glass microbeads were self-assembled into a tightly packed monolayer through the combined actions of surface tension, gravity, and lateral capillary forces at the water-air interface of a polymer solution. The packed bead monolayer was subsequently embedded in the dried polymer layer. The surface was used as a template for replicating microcavity substrates with perfect spherical shapes. We demonstrated the use of the substrate in monitoring the formation process of tumor spheroids, a proof-of-concept scale-up fabrication procedure into standard microplate formats, and its application in testing cancer drug responses in the context of bone marrow stromal cells. The presented technique offers a simple and effective way of forming high-density uniformly-sized spheroids without microfabrication equipment for biological and drug screening applications.
引用
收藏
页码:609 / 615
页数:7
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