A Simple Hanging Drop Cell Culture Protocol for Generation of 3D Spheroids

被引:484
作者
Foty, Ramsey [1 ]
机构
[1] UMDNJ Robert Wood Johnson Med Sch, Dept Surg, Piscataway, NJ USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2011年 / 51期
关键词
Bioengineering; Issue; 51; 3D; hanging drop cultures; cell sorting-out; differential adhesion;
D O I
10.3791/2720
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
Studies of cell-cell cohesion and cell-substratum adhesion have historically been performed on monolayer cultures adherent to rigid substrates. Cells within a tissue, however, are typically encased within a closely packed tissue mass in which cells establish intimate connections with many near-neighbors and with extracellular matrix components. Accordingly, the chemical milieu and physical forces experienced by cells within a 3D tissue are fundamentally different than those experienced by cells grown in monolayer culture. This has been shown to markedly impact cellular morphology and signaling. Several methods have been devised to generate 3D cell cultures including encapsulation of cells in collagen gels(1)or in biomaterial scaffolds(2). Such methods, while useful, do not recapitulate the intimate direct cell-cell adhesion architecture found in normal tissues. Rather, they more closely approximate culture systems in which single cells are loosely dispersed within a 3D meshwork of ECM products. Here, we describe a simple method in which cells are placed in hanging drop culture and incubated under physiological conditions until they form true 3D spheroids in which cells are in direct contact with each other and with extracellular matrix components. The method requires no specialized equipment and can be adapted to include addition of any biological agent in very small quantities that may be of interest in elucidating effects on cell-cell or cell-ECM interaction. The method can also be used to co-culture two (or more) different cell populations so as to elucidate the role of cell-cell or cell-ECM interactions in specifying spatial relationships between cells. Cell-cell cohesion and cell-ECM adhesion are the cornerstones of studies of embryonic development, tumor-stromal cell interaction in malignant invasion, wound healing, and for applications to tissue engineering. This simple method will provide a means of generating tissue-like cellular aggregates for measurement of biomechanical properties or for molecular and biochemical analysis in a physiologically relevant model.
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页数:4
相关论文
共 19 条
[1]
Human wound contraction: Collagen organization, fibroblasts, and myofibroblasts [J].
Berry, DP ;
Harding, KG ;
Stanton, MR ;
Jasani, B ;
Ehrlich, HP .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1998, 102 (01) :124-131
[2]
Bissell M. J., CANC RES, V59, P1757
[3]
Suppression of apoptosis by basement membrane requires three-dimensional tissue organization and withdrawal from the cell cycle [J].
Boudreau, N ;
Werb, Z ;
Bissell, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3509-3513
[4]
Cell interactions with three-dimensional matrices [J].
Cukierman, E ;
Pankov, R ;
Yamada, KM .
CURRENT OPINION IN CELL BIOLOGY, 2002, 14 (05) :633-639
[5]
Germ-layer surface tensions and "tissue affinities" in Rana pipiens gastrulae:: Quantitative measurements [J].
Davis, GS ;
Phillips, HM ;
Steinberg, MS .
DEVELOPMENTAL BIOLOGY, 1997, 192 (02) :630-644
[6]
Foty RA, 1996, DEVELOPMENT, V122, P1611
[7]
The differential adhesion hypothesis: a direct evaluation [J].
Foty, RA ;
Steinberg, MS .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :255-263
[8]
Fibroblast biology in three-dimensional collagen matrices [J].
Grinnell, F .
TRENDS IN CELL BIOLOGY, 2003, 13 (05) :264-269
[9]
Tissue surface tensions guide in vitro self-assembly of rodent pancreatic islet cells [J].
Jia, Dongxuan ;
Dajusta, Daniel ;
Foty, Ramsey A. .
DEVELOPMENTAL DYNAMICS, 2007, 236 (08) :2039-2049
[10]
Expression of the casein kinase 2 subunits in Chinese hamster ovary and 3T3 L1 cells provides information on the role of the enzyme in cell proliferation and the cell cycle [J].
Li, DX ;
Dobrowolska, G ;
Aicher, LD ;
Chen, MZ ;
Wright, JH ;
Drueckes, P ;
Dunphy, EL ;
Munar, ES ;
Krebs, EG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (46) :32988-32996