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Published on: July 17, 2016
The phenoptosis problem: what is causing the death of an organism? Lessons from acute kidney injury
D B Zorov1, E Y Plotnikov, S S Jankauskas
1Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119991, Russia. zorov@genebee.msu.su
Abstract:
Programmed execution of various cells and intracellular structures is hypothesized to be not the only example of elimination of biological systems - the general mechanism can also involve programmed execution of organs and organisms. Modern rating of programmed cell death mechanisms includes 13 mechanistic types. As for some types, the mechanism of actuation and manifestation of cell execution has been basically elucidated, while the causes and intermediate steps of the process of fatal failure of organs and organisms remain unknown. The analysis of deaths resulting from a sudden heart arrest or multiple organ failure and other acute and chronic pathologies leads to the conclusion of a special role of mitochondria and oxidative stress activating the immune system. Possible mechanisms of mitochondria-mediated induction of the signaling cascades involved in organ failure and death of the organism are discussed. These mechanisms include generation of reactive oxygen species and damage-associated molecular patterns in mitochondria. Some examples of renal failure-induced deaths are presented with mechanisms and settings determined by some hypothetical super system rather than by the kidneys themselves. This system plays the key role in the process of physiological senescence and termination of an organism. The facts presented suggest that it is the immune system involved in mitochondrial signaling that can act as the system responsible for the organism's death.
Insights
Programmed cell death extends beyond cells to organs and organisms, with mitochondria and oxidative stress potentially activating the immune system to cause organism-wide failure and death.
Area of Science:
- Biology
- Immunology
- Gerontology
Background:
- Programmed cell death is well-understood at the cellular level, but organism-level death mechanisms remain unclear.
- Existing research identifies 13 types of programmed cell death, yet the triggers for organ and organism demise are unknown.
Purpose of the Study:
- To explore the role of mitochondria and oxidative stress in organismal death.
- To investigate the immune system's involvement in programmed organ failure and organism termination.
Main Methods:
- Analysis of sudden cardiac arrest and multiple organ failure cases.
- Examination of mitochondrial signaling pathways and oxidative stress markers.
- Review of renal failure-induced deaths and hypothetical 'super-systems' controlling senescence.
Main Results:
- Mitochondria and oxidative stress appear critical in activating immune responses leading to organ failure.
- Mitochondria-derived reactive oxygen species and damage-associated molecular patterns may initiate fatal signaling cascades.
- Organismal death, including physiological senescence, might be orchestrated by an external system, potentially the immune system.
Conclusions:
- The immune system, through mitochondrial signaling, is implicated as the driver of organismal death.
- Understanding these mechanisms could reveal new therapeutic targets for age-related diseases and acute organ failure.
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