Abstract
Whether a lethally injured mammalian cell undergoes necrosis or apoptosis may be determined by the early activation of specific ion channels at the cell surface. Apoptosis requires K+ and Cl- efflux, which leads to cell shrinking, an active phenomenon termed apoptotic volume decrease (AVD). In contrast, necrosis has been shown to require Na+ influx through membrane carriers and more recently through stress-activated non-selective cation channels (NSCCs). These ubiquitous channels are kept dormant in viable cells but become activated upon exposure to free-radicals. The ensuing Na+ influx leads to cell swelling, an active response that may be termed necrotic volume increase (NVI). This review focuses on how AVD and NVI become conflicting forces at the beginning of cell injury, on the events that determine irreversibility and in particular, on the ion fluxes that decide whether a cell is to die by necrosis or by apoptosis.
Original language | English |
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Pages (from-to) | 401-409 |
Number of pages | 9 |
Journal | Comparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiology |
Volume | 130 |
Issue number | 3 |
DOIs | |
State | Published - 2001 |
Externally published | Yes |
Bibliographical note
Funding Information:We thank Claudio Hetz for helpful discussions. This work was supported by Fondecyt 1990782. Institutional support to the Centro de Estudios Cientı́ficos (CECS) from Fuerza Aérea de Chile, I. Municipalidad de Las Condes and a group of chilean private companies (AFP Provida, CODELCO, Empresas CMPC, Telefónica del Sur y Masisa S.A.) is also acknowledged. We thank support obtained through the International Program of the Howard Hughes Medical Institute and Cátedra Presidencial en Ciencias (to Francisco V. Sepúlveda). We also thank Fundación Andes for an Equipment Grant to CECS. CECS is a Millennium Science Institute.
ASJC Scopus subject areas
- Molecular Biology
- Biochemistry
- Physiology