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Bioluminescence determination of active caspase-3 in single apoptotic cells
M. Lišková, K. Klepárník, E. Matalová, J. Hegrová, J. Přikryl, E. Svandová, F. Foret,
Language English Country Germany
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Single-Cell Analysis instrumentation methods MeSH
- Apoptosis physiology MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Caspase 3 analysis metabolism MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Luminescent Measurements instrumentation methods MeSH
- Mice MeSH
- Pregnancy MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Caspase-3 is an executive caspase, in the central position within apoptotic machinery. Apoptosis as a way of programmed cell death is a physiological process that plays an essential role in the development and homeostasis maintenance; moreover, its deregulations are linked to tumor progression or various autoimmune disorders. Therefore, an investigation of apoptosis pathways on the level of individual cells is not only of biological but also medical importance. In this work we report on the development of a high-sensitivity instrumentation and protocol for detection of active caspase-3 in individual mammalian apoptotic cells. The technology is based on the specific cleavage of modified luciferin by caspase-3, an immediate bioluminescence reaction of free luciferin with luciferase followed by emissions of photons and their detection by photomultiplier tube working in the photon counting regime. Three different instrumental arrangements are compared for the determination of caspase-3 in free cells or tissue samples. Thus, in our best miniaturized system the mean amount as low as about 6.5 fg corresponding to 122 000 molecules of caspase-3 can be detected in individual apoptotic mouse leg cells.
References provided by Crossref.org
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