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Tytuł pozycji:

Regulation of caspases in the nervous system implications for functions in health and disease.

Tytuł:
Regulation of caspases in the nervous system implications for functions in health and disease.
Autorzy:
Troy CM; Department of Pathology & Cell Biology, Taub Center for the Study of Alzheimer's Disease and the Aging Brain, Columbia University College of Physicians and Surgeons, New York, USA.
Akpan N
Jean YY
Źródło:
Progress in molecular biology and translational science [Prog Mol Biol Transl Sci] 2011; Vol. 99, pp. 265-305.
Typ publikacji:
Journal Article; Review
Język:
English
Imprint Name(s):
Original Publication: Amsterdam ; Boston : Elsevier/AP
MeSH Terms:
Disease*
Health*
Caspases/*metabolism
Nervous System/*enzymology
Animals ; Caspases/chemistry ; Humans ; Nervous System/pathology ; Neurodegenerative Diseases/enzymology ; Neurodegenerative Diseases/pathology ; Neurons/enzymology ; Neurons/pathology
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Grant Information:
R01 NS035933 United States NS NINDS NIH HHS; R29 NS035933 United States NS NINDS NIH HHS
Substance Nomenclature:
EC 3.4.22.- (Caspases)
Entry Date(s):
Date Created: 20110118 Date Completed: 20110727 Latest Revision: 20220716
Update Code:
20240104
PubMed Central ID:
PMC9214546
DOI:
10.1016/B978-0-12-385504-6.00007-5
PMID:
21238939
Czasopismo naukowe
Caspases, initially identified as a family of proteases regulating cell death, have been found to have nonapoptotic functions as well. Some family members are critical for mediating programmed cell death in development. After development, caspases are downregulated in the nervous system, but continue to perform important nonapoptotic functions relevant for neurogenesis and synaptic plasticity. In neurodegenerative diseases, where aberrant neuronal death is an outstanding feature, there is an increase in caspase activity. The specific caspase death pathways leading to dysfunction and death have still not been fully clarified, despite the plethora of scientific literature addressing these issues. In this chapter, we will present the current knowledge of caspase activation and activity pathways, the current tools for examining caspases, and functions of caspases in the nervous system in health and in disease. Alzheimer's Disease, the most common neurodegenerative disorder, and cerebral ischemia, the most common cause of neurologic death, are used to illustrate our current understanding of death signaling in neurodegenerative diseases. A better understanding of how caspases function in health and disease would provide appropriate specific targets for the development of therapeutic interventions for these diseases. Life and death are exquisitely regulated at the cellular level from development through maturity. During development, neuronal death is the major factor shaping the nervous system. This death is mainly caspase-mediated apoptosis. Once the waves of developmental death have passed (death occurs at different times in different parts of the nervous system), there is downregulation of the death machinery, as the postmitotic neurons should live for the life of the organism. Aberrant neuronal death is a major part of neurodegenerative disorders, but there is still no clear understanding of the processes leading to the phenotypes of the various diseases. Even the type of death that occurs continues to be debated, whether it is apoptotic, necrotic, or autophagic, or some combination of these death mechanisms. Here, we will discuss the role that the caspases play in neuronal function, dysfunction, and death. First, we will discuss the regulation of caspase activation and activity. We will examine the current understanding of caspase function in developmental neuronal death and then illustrate the role of caspases in neuronal death in disease employing two diseases of neuronal loss, Alzheimer's Disease (AD), which is the most common chronic neurodegenerative disorder, and cerebral ischemia/stroke, the third most common cause of death in Western society, which is an acute neuronal disorder with chronic sequelae.
(Copyright © 2011 Elsevier Inc. All rights reserved.)

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