Microfluidic arrays for logarithmically perfused embryonic stem cell culture

被引:201
作者
Kim, L
Vahey, MD
Lee, HY
Voldman, J
机构
[1] MIT, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Harvard, MA USA
关键词
D O I
10.1039/b511718f
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a microfluidic device for culturing adherent cells over a logarithmic range of flow rates. The device sets flow rates through four separate cell-culture chambers using syringe-driven flow and a network of fluidic resistances. The design is easy to fabricate with no on-chip valves and is scalable both in the number of culture chambers as well as in the range of applied flow rates. Using particle velocimetry, we have characterized the flow-rate range. We have also demonstrated an extension of the design that combines the logarithmic flow-rate functionality with a logarithmic concentration gradient across the array. Using fluorescence measurements we have verified that a logarithmic concentration gradient was established in the extended device. Compared with static cell culture, both devices enable greater control over the soluble microenvironment by controlling the transport of molecules to and away from the cells. This approach is particularly relevant for cell types such as embryonic stem cells (ESCs) which are especially sensitive to the microenvironment. We have demonstrated for the first time culture of murine ESCs (mESCs) in continuous, logarithmically scaled perfusion for 4 days, with flow rates varying > 300x across the array. Cells grown in the slowest flow rate did not proliferate, while colonies grown in higher flow rates exhibited healthy round morphology. We have also demonstrated logarithmically scaled continuous perfusion culture of 3T3 fibroblasts for 3 days, with proliferation at all flow rates except the slowest rate.
引用
收藏
页码:394 / 406
页数:13
相关论文
共 33 条
[1]  
Abhyankar VV, 2003, HUMAN EMBRYONIC STEM
[2]   In vitro zonation and toxicity in a hepatocyte bioreactor [J].
Allen, JW ;
Khetani, SR ;
Bhatia, SN .
TOXICOLOGICAL SCIENCES, 2005, 84 (01) :110-119
[3]   A shear-restricted pathway of platelet procoagulant activity is regulated by IQGAP1 [J].
Bahou, WF ;
Scudder, L ;
Rubenstein, D ;
Jesty, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (21) :22571-22577
[4]   Physics and applications of microfluidics in biology [J].
Beebe, DJ ;
Mensing, GA ;
Walker, GM .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :261-286
[5]   Microfabricated platform for studying stem cell fates [J].
Chin, VI ;
Taupin, P ;
Sanga, S ;
Scheel, J ;
Gage, FH ;
Bhatia, SN .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 88 (03) :399-415
[6]  
Deen W.M., 2012, Analysis of Transport Phenomena
[7]   An extracellular matrix microarray for probing cellular differentiation [J].
Flaim, CJ ;
Chien, S ;
Bhatia, SN .
NATURE METHODS, 2005, 2 (02) :119-125
[8]   Shear-controlled single-step mouse embryonic stem cell expansion and embryoid body-based differentiation [J].
Fok, EYL ;
Zandstra, PW .
STEM CELLS, 2005, 23 (09) :1333-1342
[9]   A theoretical model study of the influence of fluid stresses on a cell adhering to a microchannel wall [J].
Gaver, DP ;
Kute, SM .
BIOPHYSICAL JOURNAL, 1998, 75 (02) :721-733
[10]   Computerized microfluidic cell culture using elastomeric channels and Braille displays [J].
Gu, W ;
Zhu, XY ;
Futai, N ;
Cho, BS ;
Takayama, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (45) :15861-15866