Abstract
Apoptosis and necrosis reflect the program of cell death employed by a dying cell and the final stage of death, respectively. Whereas apoptosis is defined as a physiological, highly organized cell death process, necrosis is commonly considered to be accidental and uncontrolled. Physiological and weak pathological death stimuli preferentially induce apoptosis, while harsh non-physiological insults often immediately instigate (primary) necrosis. If an apoptosing cell transits into a phase of plasma membrane disintegration, this stage of death is referred to as secondary or post-apoptotic necrosis.Here, we present several conditions that stimulate primary and/or secondary necrosis and show that necrosis displays considerably different time courses. For subclassification of necrotic phenotypes we employed a flow cytometric single-tube 4-color staining technique including annexin A5-FITC, propidium iodide, DiIC1(5), and Hoechst 33342.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Annexin A5 / metabolism
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Apoptosis / drug effects
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Apoptosis / radiation effects
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Benzimidazoles / metabolism
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Cell Membrane / drug effects
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Cell Membrane / metabolism
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Cell Membrane / radiation effects
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Cell Survival / drug effects
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Cell Survival / radiation effects
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DNA / metabolism
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DNA Damage
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DNA Fragmentation / drug effects
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DNA Fragmentation / radiation effects
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Flow Cytometry / methods*
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Fluorescein-5-isothiocyanate / analogs & derivatives
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Fluorescein-5-isothiocyanate / metabolism
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Freezing
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Hot Temperature
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Humans
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Hydrogen Peroxide / pharmacology
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Jurkat Cells
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Kinetics
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Melitten / pharmacology
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Mercuric Chloride / pharmacology
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Necrosis / pathology*
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Phenotype
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Propidium / metabolism
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Protein Denaturation / drug effects
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Protein Denaturation / radiation effects
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Staining and Labeling
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Ultraviolet Rays
Substances
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Annexin A5
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Benzimidazoles
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FITC-annexin A5
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Melitten
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Propidium
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Mercuric Chloride
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DNA
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Hydrogen Peroxide
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Fluorescein-5-isothiocyanate
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bisbenzimide ethoxide trihydrochloride