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Open Access
Neuronal Cell Death
Physiological reviews, 2018-04, Vol.98 (2), p.813-880
2018
Volltextzugriff (PDF)

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Autor(en) / Beteiligte
Titel
Neuronal Cell Death
Ist Teil von
  • Physiological reviews, 2018-04, Vol.98 (2), p.813-880
Ort / Verlag
United States: American Physiological Society
Erscheinungsjahr
2018
Quelle
MEDLINE
Beschreibungen/Notizen
  • Neuronal cell death occurs extensively during development and pathology, where it is especially important because of the limited capacity of adult neurons to proliferate or be replaced. The concept of cell death used to be simple as there were just two or three types, so we just had to work out which type was involved in our particular pathology and then block it. However, we now know that there are at least a dozen ways for neurons to die, that blocking a particular mechanism of cell death may not prevent the cell from dying, and that non-neuronal cells also contribute to neuronal death. We review here the mechanisms of neuronal death by intrinsic and extrinsic apoptosis, oncosis, necroptosis, parthanatos, ferroptosis, sarmoptosis, autophagic cell death, autosis, autolysis, paraptosis, pyroptosis, phagoptosis, and mitochondrial permeability transition. We next explore the mechanisms of neuronal death during development, and those induced by axotomy, aberrant cell-cycle reentry, glutamate (excitoxicity and oxytosis), loss of connected neurons, aggregated proteins and the unfolded protein response, oxidants, inflammation, and microglia. We then reassess which forms of cell death occur in stroke and Alzheimer's disease, two of the most important pathologies involving neuronal cell death. We also discuss why it has been so difficult to pinpoint the type of neuronal death involved, if and why the mechanism of neuronal death matters, the molecular overlap and interplay between death subroutines, and the therapeutic implications of these multiple overlapping forms of neuronal death.
Sprache
Englisch
Identifikatoren
ISSN: 0031-9333
eISSN: 1522-1210
DOI: 10.1152/physrev.00011.2017
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5966715

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