TY - JOUR
T1 - Microfluidic assay for simultaneous culture of multiple cell types on surfaces or within hydrogels
AU - Shin, Yoojin
AU - Han, Sewoon
AU - Jeon, Jessie S.
AU - Yamamoto, Kyoko
AU - Zervantonakis, Ioannis K.
AU - Sudo, Ryo
AU - Kamm, Roger D.
AU - Chung, Seok
N1 - Funding Information:
acknowleDGMents We acknowledge support to S.C. from the National Research Foundation of Korea (grant no. 2010-0023975), to R.S. from Japan Science and Technology Agency and Japan Society for Promotion of Science (22680037, G2212) and to R.D.K. from the National Science Foundation (CBET-0939511). We thank Y. Kikkawa, Tokyo University of Pharmacy and Life Sciences, for generously providing anti-CD146 antibody.
PY - 2012/7
Y1 - 2012/7
N2 - This protocol describes a simple but robust microfluidic assay combining three-dimensional (3D) and two-dimensional (2D) cell culture. The microfluidic platform comprises hydrogel-incorporating chambers between surface-accessible microchannels. By using this platform, well-defined biochemical and biophysical stimuli can be applied to multiple cell types interacting over distances of <1 mm, thereby replicating many aspects of the in vivo microenvironment. Capabilities exist for time-dependent manipulation of flow and concentration gradients as well as high-resolution real-time imaging for observing spatial-temporal single-cell behavior, cell-cell communication, cell-matrix interactions and cell population dynamics. These heterotypic cell type assays can be used to study cell survival, proliferation, migration, morphogenesis and differentiation under controlled conditions. Applications include the study of previously unexplored cellular interactions, and they have already provided new insights into how biochemical and biophysical factors regulate interactions between populations of different cell types. It takes 3 d to fabricate the system and experiments can run for up to several weeks.
AB - This protocol describes a simple but robust microfluidic assay combining three-dimensional (3D) and two-dimensional (2D) cell culture. The microfluidic platform comprises hydrogel-incorporating chambers between surface-accessible microchannels. By using this platform, well-defined biochemical and biophysical stimuli can be applied to multiple cell types interacting over distances of <1 mm, thereby replicating many aspects of the in vivo microenvironment. Capabilities exist for time-dependent manipulation of flow and concentration gradients as well as high-resolution real-time imaging for observing spatial-temporal single-cell behavior, cell-cell communication, cell-matrix interactions and cell population dynamics. These heterotypic cell type assays can be used to study cell survival, proliferation, migration, morphogenesis and differentiation under controlled conditions. Applications include the study of previously unexplored cellular interactions, and they have already provided new insights into how biochemical and biophysical factors regulate interactions between populations of different cell types. It takes 3 d to fabricate the system and experiments can run for up to several weeks.
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U2 - 10.1038/nprot.2012.051
DO - 10.1038/nprot.2012.051
M3 - Article
C2 - 22678430
AN - SCOPUS:84862157431
SN - 1754-2189
VL - 7
SP - 1247
EP - 1259
JO - Nature Protocols
JF - Nature Protocols
IS - 7
ER -