Issue 11, 2022

Live single cell imaging assays in glass microwells produced by laser-induced deep etching

Abstract

Miniaturization of cell culture substrates enables controlled analysis of living cells in confined micro-scale environments. This is particularly suitable for imaging individual cells over time, as they can be monitored without escaping the imaging field-of-view (FoV). Glass materials are ideal for most microscopy applications. However, with current methods used in life sciences, glass microfabrication is limited in terms of either freedom of design, quality, or throughput. In this work, we introduce laser-induced deep etching (LIDE) as a method for producing glass microwell arrays for live single cell imaging assays. We demonstrate novel microwell arrays with deep, high-aspect ratio wells that have rounded, dimpled or flat bottom profiles in either single-layer or double-layer glass chips. The microwells are evaluated for microscopy-based analysis of long-term cell culture, clonal expansion, laterally organized cell seeding, subcellular mechanics during migration and immune cell cytotoxicity assays of both adherent and suspension cells. It is shown that all types of microwells can support viable cell cultures and imaging with single cell resolution, and we highlight specific benefits of each microwell design for different applications. We believe that high-quality glass microwell arrays enabled by LIDE provide a great option for high-content and high-resolution imaging-based live cell assays with a broad range of potential applications within life sciences.

Graphical abstract: Live single cell imaging assays in glass microwells produced by laser-induced deep etching

Supplementary files

Article information

Article type
Paper
Submitted
27 Jan 2022
Accepted
07 Apr 2022
First published
07 Apr 2022
This article is Open Access
Creative Commons BY license

Lab Chip, 2022,22, 2107-2121

Live single cell imaging assays in glass microwells produced by laser-induced deep etching

N. Sandström, L. Brandt, P. A. Sandoz, C. Zambarda, K. Guldevall, M. Schulz-Ruhtenberg, B. Rösener, R. A. Krüger and B. Önfelt, Lab Chip, 2022, 22, 2107 DOI: 10.1039/D2LC00090C

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