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Updated: May 3, 2026

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
Published on: April 9, 2014
Pulsetrain-burst mode, ultrafast-laser interactions with 3D viable cell cultures as a model for soft biological
Zuoming Qian1, Aghapi Mordovanakis2, Joshua E Schoenly1
1Department of Physics, & Institute for Optical Sciences, University of Toronto, 60 St. George Street, Toronto ON M5S 1A7, Canada.
Abstract:
A 3D living-cell culture in hydrogel has been developed as a standardized low-tensile-strength tissue proxy for study of ultrafast, pulsetrain-burst laser-tissue interactions. The hydrogel is permeable to fluorescent biomarkers and optically transparent, allowing viable and necrotic cells to be imaged in 3D by confocal microscopy. Good cell-viability allowed us to distinguish between typical cell mortality and delayed subcellular tissue damage (e.g., apoptosis and DNA repair complex formation), caused by laser irradiation. The range of necrosis depended on laser intensity, but not on pulsetrain-burst duration. DNA double-strand breaks were quantified, giving a preliminary upper limit for genetic damage following laser treatment.

