![]() The main challenges are ( i) inking cells to their molds with precision and maintaining viability, ( ii) evenly and gently applying and transferring the cells to a substrate and successfully lifting off the mold without detaching the cells, and ( iii) maintaining cell functions after printing. However, application of the block-printing concept to cells has never been achieved. In particular, woodblock printing is an efficient and convenient technology that revolutionized the printing world more than 1,800 y ago and was extended to microcontact molecular printing ∼20 y ago ( 24). ![]() Potentially useful and convenient tools may be available by adapting traditional printing tools to cell printing. However, finding a method that completely satisfies the above requirements remains a challenge. Several approaches have been designed for this purpose, e.g., inkjet cell printing ( 3– 6), surface engineering ( 7– 15), and physical constraints ( 16– 23). Furthermore, primary neurons are also compatible with BloC-Printing.Ĭurrent high-throughput screening of cell function and heterogeneity and in vitro cell–cell communication studies requires routine generation of large-scale single-cell arrays with high precision and efficiency, single-cell resolution, multiple cell types, and maintenance of cell viability and function ( 1, 2). 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. 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. ![]() The approach enables the large-scale formation of heterotypic cell pairs with controlled morphology and allows for material transport through gap junction intercellular communication. 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. 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. 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.
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