Intracellular and Intercellular Mitochondrial Dynamics in Parkinson’s Disease
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F86652036%3A_____%2F19%3A00521553" target="_blank" >RIV/86652036:_____/19:00521553 - isvavai.cz</a>
Result on the web
<a href="https://www.frontiersin.org/articles/10.3389/fnins.2019.00930/full" target="_blank" >https://www.frontiersin.org/articles/10.3389/fnins.2019.00930/full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fnins.2019.00930" target="_blank" >10.3389/fnins.2019.00930</a>
Alternative languages
Result language
angličtina
Original language name
Intracellular and Intercellular Mitochondrial Dynamics in Parkinson’s Disease
Original language description
The appearance of alpha-synuclein-positive inclusion bodies (Lewy bodies) and the loss of catecholaminergic neurons are the primary pathological hallmarks of Parkinson’s disease (PD). However, the dysfunction of mitochondria has long been recognized as a key component in the progression of the disease. Dysfunctional mitochondria can in turn lead to dysregulation of calcium homeostasis and, especially in dopaminergic neurons, raised mean intracellular calcium concentration. As calcium binding to alpha-synuclein is one of the important triggers of alpha-synuclein aggregation, mitochondrial dysfunction will promote inclusion body formation and disease progression. Increased reactive oxygen species (ROS) resulting from inefficiencies in the electron transport chain also contribute to the formation of alpha-synuclein aggregates and neuronal loss. Recent studies have also highlighted defects in mitochondrial clearance that lead to the accumulation of depolarized mitochondria. Transaxonal and intracytoplasmic translocation of mitochondria along the microtubule cytoskeleton may also be affected in diseased neurons. Furthermore, nanotube-mediated intercellular transfer of mitochondria has recently been reported between different cell types and may have relevance to the spread of PD pathology between adjacent brain regions. In the current review, the contributions of both intracellular and intercellular mitochondrial dynamics to the etiology of PD will be discussed.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30103 - Neurosciences (including psychophysiology)
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
FRONT NEUROSCI-SWITZ
ISSN
1662-4548
e-ISSN
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Volume of the periodical
13
Issue of the periodical within the volume
SEP 18 2019
Country of publishing house
GB - UNITED KINGDOM
Number of pages
8
Pages from-to
930
UT code for WoS article
000486406800001
EID of the result in the Scopus database
2-s2.0-85072898645