Issue 21, 2010

Micromolded arrays for separation of adherent cells

Abstract

We present an efficient, yet inexpensive, approach for isolating viable single cells or colonies from a mixed population. This cell microarray platform possesses innovations in both the array manufacture and the manner of target cell release. Arrays of microwells with bases composed of detachable concave elements, termed microrafts, were fabricated by a dip-coating process using a polydimethylsiloxane mold as the template and the array substrate. This manufacturing approach enabled the use of materials other than photoresists to create the array elements. Thus microrafts possessing low autofluorescence could be fabricated for fluorescence-based identification of cells. Cells plated on the microarray settled and attached at the center of the wells due to the microrafts' concavity. Individual microrafts were readily dislodged by the action of a needle inserted through the compliant polymer substrate. The hard polymer material (polystyrene or epoxy resin) of which the microrafts were composed protected the cells from damage by the needle. For cell analysis and isolation, cells of interest were identified using a standard inverted microscope and microrafts carrying target cells were dislodged with the needle. The released cells/microrafts could be efficiently collected, cultured and clonally expanded. During the separation and collection procedures, the cells remained adherent and provided a measure of protection during manipulation, thus providing an extremely high single-cell cloning rate (>95%). Generation of a transfected cell line based on expression of a fluorescent protein demonstrated an important application for performing on-chip cell separations.

Graphical abstract: Micromolded arrays for separation of adherent cells

Supplementary files

Article information

Article type
Paper
Submitted
09 Jul 2010
Accepted
17 Aug 2010
First published
13 Sep 2010

Lab Chip, 2010,10, 2917-2924

Micromolded arrays for separation of adherent cells

Y. Wang, C. Phillips, W. Xu, J. Pai, R. Dhopeshwarkar, C. E. Sims and N. Allbritton, Lab Chip, 2010, 10, 2917 DOI: 10.1039/C0LC00186D

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