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Oxytosis/Ferroptosis-(Re-) Emerging Roles for Oxidative Stress-Dependent Non-apoptotic Cell Death in Diseases of the Central Nervous System
被引:214
|作者:
Lewerenz, Jan
[1
]
Ates, Gamze
[2
]
Methner, Axel
[3
,4
]
Conrad, Marcus
[5
]
Maher, Pamela
[2
]
机构:
[1] Ulm Univ, Dept Neurol, Ulm, Germany
[2] Salk Inst Biol Studies, Cellular Neurobiol Lab, 10010 N Torrey Pines Rd, La Jolla, CA 92037 USA
[3] Johannes Gutenberg Univ Mainz, Dept Neurol, Univ Med Ctr, Mainz, Germany
[4] Johannes Gutenberg Univ Mainz, Focus Program Translat Neurosci, Mainz, Germany
[5] Helmholtz Zentrum Munchen, Inst Dev Genet, Neuherberg, Germany
来源:
关键词:
programmed cell death;
oxytosis;
ferroptosis;
iron;
oxidative stress;
brain diseases;
GLUTATHIONE-PEROXIDASE;
4;
AMYOTROPHIC-LATERAL-SCLEROSIS;
MOTOR-NEURON DEGENERATION;
POLYUNSATURATED FATTY-ACIDS;
LACKING MITOCHONDRIAL-DNA;
GLOBAL CEREBRAL-ISCHEMIA;
ONSET ALZHEIMERS-DISEASE;
TRANSGENIC MOUSE MODEL;
TUMOR-NECROSIS-FACTOR;
MIXED LINEAGE KINASE;
D O I:
10.3389/fnins.2018.00214
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Although nerve cell death is the hallmark of many neurological diseases, the processes underlying this death are still poorly defined. However, there is a general consensus that neuronal cell death predominantly proceeds by regulated processes. Almost 30 years ago, a cell death pathway eventually named oxytosis was described in neuronal cells that involved glutathione depletion, reactive oxygen species production, lipoxygenase activation, and calcium influx. More recently, a cell death pathway that involved many of the same steps was described in tumor cells and termed ferroptosis due to a dependence on iron. Since then there has been a great deal of discussion in the literature about whether these are two distinct pathways or cell type- and insult-dependent variations on the same pathway. In this review, we compare and contrast in detail the commonalities and distinctions between the two pathways concluding that the molecular pathways involved in the regulation of ferroptosis and oxytosis are highly similar if not identical. Thus, we suggest that oxytosis and ferroptosis should be regarded as two names for the same cell death pathway. In addition, we describe the potential physiological relevance of oxytosis/ferroptosis in multiple neurological diseases.
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