Pulsed Laser Microbeam-Induced Cell Lysis: Time-Resolved Imaging and Analysis of Hydrodynamic Effects

• Published in: Biophysical journal Vol. 91; no. 1; pp. 317 - 329
• Main Authors: Rau, Kaustubh R., Quinto-Su, Pedro A., Hellman, Amy N., Venugopalan, Vasan
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.07.2006; Biophysical Society
• Subjects: Animals; Biophysics; Cavitation; Cell Fractionation - instrumentation; Cell Fractionation - methods; Cell Line; Cellular biology; Computer Simulation; Epithelial Cells - cytology; Epithelial Cells - physiology; Epithelial Cells - radiation effects; Equipment Design; Equipment Failure Analysis; Irradiation; Kidney - cytology; Kidney - physiology; Kidney - radiation effects; Lasers; Microscopy, Fluorescence - instrumentation; Microscopy, Fluorescence - methods; Models, Biological; Molecular biology; Photolysis - radiation effects; Rats; Scientific imaging; Shear stress; Spectroscopy, Imaging Other Techniques; Wave propagation
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1529/biophysj.105.079921

Time-resolved imaging was used to examine the use of pulsed laser microbeam irradiation to produce cell lysis. Lysis was accomplished through the delivery of 6 ns, λ = 532 nm laser pulses via a 40×, 0.8 NA objective to a location 10 μm above confluent monolayers of PtK 2 cells. The process dynamics were examined at cell surface densities of 600 and 1000 cells/mm 2 and pulse energies corresponding to 0.7×, 1×, 2×, and 3× the threshold for plasma formation. The cell lysis process was imaged at times of 0.5 ns to 50 μs after laser pulse delivery and revealed the processes of plasma formation, pressure wave propagation, and cavitation bubble dynamics. Cavitation bubble expansion was the primary agent of cell lysis with the zone of lysed cells fully established within 600 ns of laser pulse delivery. The spatial extent of cell lysis increased with pulse energy but decreased with cell surface density. Hydrodynamic analysis indicated that cells subject to transient shear stresses in excess of a critical value were lysed while cells exposed to lower shear stresses remained adherent and viable. This critical shear stress is independent of laser pulse energy and varied from ∼60–85 kPa for cell monolayers cultured at a density of 600 cells/mm 2 to ∼180–220 kPa for a surface density of 1000 cells/mm 2. The implications for single cell lysis and microsurgery are discussed.