Single Cell Responses to Spatially Controlled Photosensitized Production of Extracellular Singlet Oxygen

The response of individual HeLa cells to extracellularly produced singlet oxygen was examined. The spatial domain of singlet oxygen production was controlled using the combination of a membrane‐impermeable Pd porphyrin‐dendrimer, which served as a photosensitizer, and a focused laser, which served t...

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Veröffentlicht in:Photochemistry and photobiology 2011-09, Vol.87 (5), p.1077-1091
Hauptverfasser: Pedersen, Brian W., Sinks, Louise E., Breitenbach, Thomas, Schack, Nickolass B., Vinogradov, Sergei A., Ogilby, Peter R.
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container_end_page 1091
container_issue 5
container_start_page 1077
container_title Photochemistry and photobiology
container_volume 87
creator Pedersen, Brian W.
Sinks, Louise E.
Breitenbach, Thomas
Schack, Nickolass B.
Vinogradov, Sergei A.
Ogilby, Peter R.
description The response of individual HeLa cells to extracellularly produced singlet oxygen was examined. The spatial domain of singlet oxygen production was controlled using the combination of a membrane‐impermeable Pd porphyrin‐dendrimer, which served as a photosensitizer, and a focused laser, which served to localize the sensitized production of singlet oxygen. Cells in close proximity to the domain of singlet oxygen production showed morphological changes commonly associated with necrotic cell death. The elapsed postirradiation “waiting period” before necrosis became apparent depended on: (1) the distance between the cell membrane and the domain irradiated, (2) the incident laser fluence and, as such, the initial concentration of singlet oxygen produced and (3) the lifetime of singlet oxygen. The data imply that singlet oxygen plays a key role in this process of light‐induced cell death. The approach of using extracellularly generated singlet oxygen to induce cell death can provide a solution to a problem that often limits mechanistic studies of intracellularly photosensitized cell death: it can be difficult to quantify the effective light dose, and hence singlet oxygen concentration, when using an intracellular photosensitizer. Use of extracellularly generated singlet oxygen can provide helpful insight in mechanistic studies of cell death.
doi_str_mv 10.1111/j.1751-1097.2011.00951.x
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The spatial domain of singlet oxygen production was controlled using the combination of a membrane‐impermeable Pd porphyrin‐dendrimer, which served as a photosensitizer, and a focused laser, which served to localize the sensitized production of singlet oxygen. Cells in close proximity to the domain of singlet oxygen production showed morphological changes commonly associated with necrotic cell death. The elapsed postirradiation “waiting period” before necrosis became apparent depended on: (1) the distance between the cell membrane and the domain irradiated, (2) the incident laser fluence and, as such, the initial concentration of singlet oxygen produced and (3) the lifetime of singlet oxygen. The data imply that singlet oxygen plays a key role in this process of light‐induced cell death. The approach of using extracellularly generated singlet oxygen to induce cell death can provide a solution to a problem that often limits mechanistic studies of intracellularly photosensitized cell death: it can be difficult to quantify the effective light dose, and hence singlet oxygen concentration, when using an intracellular photosensitizer. 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subjects Apoptosis
Cell Death - drug effects
Cell Death - radiation effects
Cell Membrane - drug effects
Cell Membrane - radiation effects
Cells
Extracellular Space
Female
HeLa Cells
Humans
Lasers
Mesoporphyrins - pharmacology
Metalloporphyrins - pharmacology
Microscopy
Morphology
Mortality
Oxygen
Photobiology
Photochemotherapy - methods
Photosensitizing Agents - pharmacology
Photosynthesis
Single-Cell Analysis - instrumentation
Single-Cell Analysis - methods
Singlet Oxygen - adverse effects
Singlet Oxygen - metabolism
Ultraviolet Rays
title Single Cell Responses to Spatially Controlled Photosensitized Production of Extracellular Singlet Oxygen
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