Maskless liquid-crystal-display projection photolithography for improved design flexibility of cellular micropatterns.

We previously developed an all-in-one photopolymerization device by modifying a commercially available liquid crystal display projector (LCDP) for the preparation of micropatterned surfaces and microfluidic channels without the need for expensive photomasks. In the present study, we demonstrate a simple and reliable method for rapid prototyping of cell micropatterning with high resolution using the modified LCDP device. Fabrication of complicated and flexible patterns was achieved using this device with positive-type photoresist in a two-step process. First, micropatterns on the silanized coverslips were fabricated from positive photoresist. Second, acrylamide monomer solution containing polymerization initiator was dropped onto the micropatterned positive photoresist and copolymerized on the silanized coverslips in situ by thermally initiated radical polymerization. After the reaction, the remnant micropatterned photoresist is easily dissolved, resulting in a polyacrylamide-silane micropattern on the coverslip. The resultant polyacrylamide layer is highly hydrophilic and repels both protein adsorption and cell adhesion. Cells seeded on the micropatterned surfaces therefore attach and spread only on unpolymerized silanized glass surfaces, conforming to the pattern design. This technique is therefore useful for inexpensive, rapid prototyping of surface micropatterns using polymer materials.

[1]  Masayuki Yamato,et al.  Micropatterned surfaces prepared using a liquid crystal projector-modified photopolymerization device and microfluidics. , 2004, Journal of biomedical materials research. Part A.

[2]  Daniel I. C. Wang,et al.  Engineering cell shape and function. , 1994, Science.

[3]  K E Healy,et al.  Surfaces designed to control the projected area and shape of individual cells. , 1999, Journal of biomechanical engineering.

[4]  Kevin E. Healy,et al.  Engineering gene expression and protein synthesis by modulation of nuclear shape , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[5]  S. P. Fodor,et al.  Light-generated oligonucleotide arrays for rapid DNA sequence analysis. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[6]  A. Mirzabekov,et al.  Protein microchips: use for immunoassay and enzymatic reactions. , 2000, Analytical biochemistry.

[7]  D Kleinfeld,et al.  Controlled outgrowth of dissociated neurons on patterned substrates , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  Masayuki Yamato,et al.  Preparation of Microfluidic Devices Using Micropatterning of a Photosensitive Material by a Maskless, Liquid‐Crystal‐Display Projection Method , 2004 .

[9]  S. P. Fodor,et al.  Light-directed, spatially addressable parallel chemical synthesis. , 1991, Science.

[10]  T. Kunitake,et al.  Chemical modification of molecularly smooth mica surface and protein attachment , 1994 .

[11]  Masayuki Yamato,et al.  Cell micropatterning using photopolymerization with a liquid crystal device commercial projector. , 2004, Biomaterials.

[12]  W. Godwin Article in Press , 2000 .

[13]  S. Hubchak,et al.  P(AAm-co-EG) Interpenetrating Polymer Networks Grafted to Oxide Surfaces: Surface Characterization, Protein Adsorption, and Cell Detachment Studies , 1997 .

[14]  C. S. Chen,et al.  Geometric control of cell life and death. , 1997, Science.

[15]  M L Yarmush,et al.  Controlling cell interactions by micropatterning in co-cultures: hepatocytes and 3T3 fibroblasts. , 1997, Journal of biomedical materials research.

[16]  R. Misra,et al.  Biomaterials , 2008 .

[17]  Marcus Textor,et al.  A Combined Photolithographic and Molecular‐Assembly Approach to Produce Functional Micropatterns for Applications in the Biosciences , 2004 .

[18]  D. Sabatini,et al.  Microarrays of cells expressing defined cDNAs , 2001, Nature.

[19]  L. Griffith,et al.  A microfabricated array bioreactor for perfused 3D liver culture. , 2002, Biotechnology and bioengineering.

[20]  Stellan Hjertén,et al.  High-performance electrophoresis : Elimination of electroendosmosis and solute adsorption , 1985 .

[21]  George M. Whitesides,et al.  Rapid prototyping of complex structures with feature sizes larger than 20 μm , 1996 .

[22]  T. Okano,et al.  Thermosensitive Phase-Separation Behavior of Poly(acrylic acid)-graft-poly(N,N-dimethylacrylamide) Aqueous Solution , 2000 .