TY - JOUR
T1 - Block-Cell-Printing for live single-cell printing
AU - Zhang, Kai
AU - Chou, Chao Kai
AU - Xia, Xiaofeng
AU - Hung, Mien Chie
AU - Qin, Lidong
PY - 2014/2/25
Y1 - 2014/2/25
N2 - A unique live-cell printing technique, termed "Block-Cell- Printing" (BloC-Printing), allows for convenient, precise, multiplexed, and high-throughput printing of functional single-cell arrays. Adapted from woodblock printing techniques, the approach employs microfluidic arrays of hook-shaped traps to hold cells at designated positions and directly transfer the anchored cells onto various substrates. BloC-Printing has a minimum turnaround time of 0.5 h, a maximum resolution of 5 μm, close to 100% cell viability, the ability to handle multiple cell types, and efficiently construct protrusion-connected single-cell arrays. The approach enables the large-scale formation of heterotypic cell pairs with controlled morphology and allows for material transport through gap junction intercellular communication. When six types of breast cancer cells are allowed to extend membrane protrusions in the BloC-Printing device for 3 h, multiple biophysical characteristics of cells - including the protrusion percentage, extension rate, and cell length - are easily quantified and found to correlate well with their migration levels. In light of this discovery, BloC-Printing may serve as a rapid and high-throughput cell protrusion characterization tool to measure the invasion and migration capability of cancer cells. Furthermore, primary neurons are also compatible with BloC-Printing.
AB - A unique live-cell printing technique, termed "Block-Cell- Printing" (BloC-Printing), allows for convenient, precise, multiplexed, and high-throughput printing of functional single-cell arrays. Adapted from woodblock printing techniques, the approach employs microfluidic arrays of hook-shaped traps to hold cells at designated positions and directly transfer the anchored cells onto various substrates. BloC-Printing has a minimum turnaround time of 0.5 h, a maximum resolution of 5 μm, close to 100% cell viability, the ability to handle multiple cell types, and efficiently construct protrusion-connected single-cell arrays. The approach enables the large-scale formation of heterotypic cell pairs with controlled morphology and allows for material transport through gap junction intercellular communication. When six types of breast cancer cells are allowed to extend membrane protrusions in the BloC-Printing device for 3 h, multiple biophysical characteristics of cells - including the protrusion percentage, extension rate, and cell length - are easily quantified and found to correlate well with their migration levels. In light of this discovery, BloC-Printing may serve as a rapid and high-throughput cell protrusion characterization tool to measure the invasion and migration capability of cancer cells. Furthermore, primary neurons are also compatible with BloC-Printing.
KW - Cell array
KW - Cell communication
KW - Neuron patterning
KW - Protrusion profiling
UR - http://www.scopus.com/inward/record.url?scp=84896811634&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84896811634&partnerID=8YFLogxK
U2 - 10.1073/pnas.1313661111
DO - 10.1073/pnas.1313661111
M3 - Article
C2 - 24516129
AN - SCOPUS:84896811634
VL - 111
SP - 2948
EP - 2953
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
SN - 0027-8424
IS - 8
ER -