Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease

Parkinson’s disease (PD) is a neurodegenerative disorder caused by insufficient dopamine production due to the loss of 50% to 70% of dopaminergic neurons. A shortage of dopamine, which is predominantly produced by the dopaminergic neurons within the substantia nigra, causes clinical sympto...

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Main Authors: Anastasiia Bohush, Grazyna Niewiadomska, Anna Filipek
Format: Article
Language:English
Published: MDPI AG 2018-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/10/2973
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spelling doaj-24bc5b2a5252496dab657d9f6cb7aabf2020-11-25T02:28:58ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-09-011910297310.3390/ijms19102973ijms19102973Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s DiseaseAnastasiia Bohush0Grazyna Niewiadomska1Anna Filipek2Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, PolandNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, PolandNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, PolandParkinson’s disease (PD) is a neurodegenerative disorder caused by insufficient dopamine production due to the loss of 50% to 70% of dopaminergic neurons. A shortage of dopamine, which is predominantly produced by the dopaminergic neurons within the substantia nigra, causes clinical symptoms such as reduction of muscle mass, impaired body balance, akinesia, bradykinesia, tremors, postural instability, etc. Lastly, this can lead to a total loss of physical movement and death. Since no cure for PD has been developed up to now, researchers using cell cultures and animal models focus their work on searching for potential therapeutic targets in order to develop effective treatments. In recent years, genetic studies have prominently advocated for the role of improper protein phosphorylation caused by a dysfunction in kinases and/or phosphatases as an important player in progression and pathogenesis of PD. Thus, in this review, we focus on the role of selected MAP kinases such as JNKs, ERK1/2, and p38 MAP kinases in PD pathology.http://www.mdpi.com/1422-0067/19/10/2973apoptosisERK1/2JNKsmitochondrial dysfunctionneurodegenerationneuro-inflammationoxidative stressp38 MAPKsParkinson’s disease
collection DOAJ
language English
format Article
sources DOAJ
author Anastasiia Bohush
Grazyna Niewiadomska
Anna Filipek
spellingShingle Anastasiia Bohush
Grazyna Niewiadomska
Anna Filipek
Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
International Journal of Molecular Sciences
apoptosis
ERK1/2
JNKs
mitochondrial dysfunction
neurodegeneration
neuro-inflammation
oxidative stress
p38 MAPKs
Parkinson’s disease
author_facet Anastasiia Bohush
Grazyna Niewiadomska
Anna Filipek
author_sort Anastasiia Bohush
title Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
title_short Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
title_full Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
title_fullStr Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
title_full_unstemmed Role of Mitogen Activated Protein Kinase Signaling in Parkinson’s Disease
title_sort role of mitogen activated protein kinase signaling in parkinson’s disease
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-09-01
description Parkinson’s disease (PD) is a neurodegenerative disorder caused by insufficient dopamine production due to the loss of 50% to 70% of dopaminergic neurons. A shortage of dopamine, which is predominantly produced by the dopaminergic neurons within the substantia nigra, causes clinical symptoms such as reduction of muscle mass, impaired body balance, akinesia, bradykinesia, tremors, postural instability, etc. Lastly, this can lead to a total loss of physical movement and death. Since no cure for PD has been developed up to now, researchers using cell cultures and animal models focus their work on searching for potential therapeutic targets in order to develop effective treatments. In recent years, genetic studies have prominently advocated for the role of improper protein phosphorylation caused by a dysfunction in kinases and/or phosphatases as an important player in progression and pathogenesis of PD. Thus, in this review, we focus on the role of selected MAP kinases such as JNKs, ERK1/2, and p38 MAP kinases in PD pathology.
topic apoptosis
ERK1/2
JNKs
mitochondrial dysfunction
neurodegeneration
neuro-inflammation
oxidative stress
p38 MAPKs
Parkinson’s disease
url http://www.mdpi.com/1422-0067/19/10/2973
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