Synthesis of Cell-Adhesive Anisotropic Multifunctional Particles by Stop Flow Lithography and Streptavidin-Biotin Interactions

被引:30
作者
Bong, Ki Wan [1 ,2 ]
Kim, Jae Jung [3 ]
Cho, Hansang [1 ]
Lim, Eugene [1 ]
Doyle, Patrick S. [3 ]
Irimia, Daniel [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Engn Med & Surg Serv, Charlestown, MA 02129 USA
[2] Korea Univ, Dept Chem & Biol Engn, Seoul 136713, South Korea
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MICROPARTICLES; PROTEIN; 3D; MICROSTRUCTURES; MICROARRAYS; CAPILLARY; TRANSPORT; RELEASE;
D O I
10.1021/acs.langmuir.5b03501
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Cell-adhesive particles are of significant interest in biotechnology, the bioengineering of complex tissues, and biomedical research. Their applications range from platforms to increase the efficiency of anchorage-dependent cell culture to building blocks to loading cells in heterogeneous structures to clonal-population growth monitoring to cell sorting. Although useful, currently available cell-adhesive particles can accommodate only homogeneous cell culture. Here, we report the design of anisotropic hydrogel microparticles with tunable cell-adhesive regions as first step toward micropatterned cell cultures on particles. We employed stop flow lithography (SFL), the coupling reaction between amine and N-hydroxysuccinimide (NHS) and streptavidin biotin chemistry to adjust the localization of conjugated collagen and poly-L-lysine on the surface of microscale particles. Using the new particles, we demonstrate the attachment and formation of tight junctions between brain endothelial cells. We also demonstrate the geometric patterning of breast cancer cells on particles with heterogeneous collagen coatings. This new approach avoids the exposure of cells to potentially toxic photoinitiators and ultraviolet light and decouples in time the microparticle synthesis and the cell culture steps to take advantage of the most recent advances in cell patterning available for traditional culture substrates.
引用
收藏
页码:13165 / 13171
页数:7
相关论文
共 34 条
[1]
Multiplexed Protein Quantification with Barcoded Hydrogel Microparticles [J].
Appleyard, David C. ;
Chapin, Stephen C. ;
Doyle, Patrick S. .
ANALYTICAL CHEMISTRY, 2011, 83 (01) :193-199
[2]
Non-polydimethylsiloxane devices for oxygen-free flow lithography [J].
Bong, Ki Wan ;
Xu, Jingjing ;
Kim, Jong-Ho ;
Chapin, Stephen C. ;
Strano, Michael S. ;
Gleason, Karen K. ;
Doyle, Patrick S. .
NATURE COMMUNICATIONS, 2012, 3
[3]
Compressed-air flow control system [J].
Bong, Ki Wan ;
Chapin, Stephen C. ;
Pregibon, Daniel C. ;
Baah, David ;
Floyd-Smith, Tamara M. ;
Doyle, Patrick S. .
LAB ON A CHIP, 2011, 11 (04) :743-747
[4]
Hydrodynamic Focusing Lithography [J].
Bong, Ki Wan ;
Bong, Ki Tae ;
Pregibon, Daniel C. ;
Doyle, Patrick S. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (01) :87-90
[5]
Lock release lithography for 3D and composite microparticles [J].
Bong, Ki Wan ;
Pregibon, Daniel C. ;
Doyle, Patrick S. .
LAB ON A CHIP, 2009, 9 (07) :863-866
[6]
Rapid microRNA Profiling on Encoded Gel Microparticles [J].
Chapin, Stephen C. ;
Appleyard, David C. ;
Pregibon, Daniel C. ;
Doyle, Patrick S. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (10) :2289-2293
[7]
Guided and fluidic self-assembly of microstructures using railed microfluidic channels [J].
Chung, Su Eun ;
Park, Wook ;
Shin, Sunghwan ;
Lee, Seung Ah ;
Kwon, Sunghoon .
NATURE MATERIALS, 2008, 7 (07) :581-587
[8]
One-step pipetting and assembly of encoded chemical-laden microparticles for high-throughput multiplexed bioassays [J].
Chung, Su Eun ;
Kim, Jiyun ;
Oh, Dong Yoon ;
Song, Younghoon ;
Lee, Sung Hoon ;
Min, Seungki ;
Kwon, Sunghoon .
NATURE COMMUNICATIONS, 2014, 5
[9]
Continuous-flow lithography for high-throughput microparticle synthesis [J].
Dendukuri, D ;
Pregibon, DC ;
Collins, J ;
Hatton, TA ;
Doyle, PS .
NATURE MATERIALS, 2006, 5 (05) :365-369
[10]
Dendukuri D, 2007, LAB CHIP, V7, P818, DOI 10.1039/b703457a