Nuclear apoptotic volume decrease in individual cells: Confocal microscopy imaging and kinetic modeling
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29859212
DOI
10.1016/j.jtbi.2018.05.034
PII: S0022-5193(18)30281-9
Knihovny.cz E-zdroje
- Klíčová slova
- 3D time lapsed confocal microscopy, Apoptosis, Apoptotic ring, Chromatin condensation, Kinetics, Live cell analysis, Mathematical modeling, Nuclear volume decrease,
- MeSH
- analýza jednotlivých buněk metody MeSH
- apoptóza fyziologie MeSH
- buněčné jádro fyziologie ultrastruktura MeSH
- buňky Hep G2 MeSH
- časosběrné zobrazování metody MeSH
- chromatin chemie metabolismus ultrastruktura MeSH
- kinetika MeSH
- konfokální mikroskopie MeSH
- lidé MeSH
- sbalení DNA MeSH
- teoretické modely * MeSH
- velikost organel fyziologie MeSH
- zobrazování trojrozměrné MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chromatin MeSH
The dynamics of nuclear morphology changes during apoptosis remains poorly investigated and understood. Using 3D time-lapse confocal microscopy we performed a study of early-stage apoptotic nuclear morphological changes induced by etoposide in single living HepG2 cells. These observations provide a definitive evidence that nuclear apoptotic volume decrease (AVD) is occurring simultaneously with peripheral chromatin condensation (so called "apoptotic ring"). In order to describe quantitatively the dynamics of nuclear morphological changes in the early stage of apoptosis we suggest a general molecular kinetic model, which fits well the obtained experimental data in our study. Results of this work may clarify molecular mechanisms of nuclear morphology changes during apoptosis.
Department of Genetics Stanford University Campus Drive 279 Stanford CA 94305 USA
Voevodsky Institute of Chemical Kinetics and Combustion Institutskaya 3 Novosibirsk 630090 Russia
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