miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway

Differential expression of microRNAs (miRs) in the brain of patients with neurodegenerative diseases suggests that they may have key regulatory roles in the development of these disorders. Two such miRs, miR-7 and miR-153 have recently been shown to target α-synuclein, a protein critically involved...

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Main Authors: Apostolia eFragkouli, Epaminondas eDoxakis
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-07-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00182/full
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author Apostolia eFragkouli
Epaminondas eDoxakis
author_facet Apostolia eFragkouli
Epaminondas eDoxakis
author_sort Apostolia eFragkouli
collection DOAJ
description Differential expression of microRNAs (miRs) in the brain of patients with neurodegenerative diseases suggests that they may have key regulatory roles in the development of these disorders. Two such miRs, miR-7 and miR-153 have recently been shown to target α-synuclein, a protein critically involved in the pathological process of Parkinson’s disease. By using a well-established in culture Parkinson’s disease model that of neurotoxin 1-Methyl-4-Phenyl-Pyridinium (MPP+), we examined whether miR-7 and miR-153 display neuroprotective properties. Herein, we demonstrate that treatment of cortical neurons with MPP+ induced a dose-dependent cell death with apoptotic characteristics. This was reflected in altered intracellular signaling characterized by increased levels of activated kinases p38MAPK and ERK1/2 and reduced levels of activated AKT, p70S6K and SAPK/JNK. Overexpression of miR-7 or miR-153 by adenoviral transduction protected cortical neurons from MPP+-induced toxicity, restored neuronal viability and anti-apoptotic BCL-2 protein levels while attenuated activation of caspase-3. Moreover, both miR-7 and miR-153 interfered with MPP+-induced alterations in intracellular signaling pathways in a partially overlapping manner; specifically, they preserved activation of mTOR and SAPK/JNK signaling pathways in the MPP+-treated neurons, while miR-153 also attenuated MPP+-induced activation of p38MAPK. No major effects were observed in the rest of signaling cascades or proteins investigated. Furthermore, the neuroprotective effect of miR-7 and miR-153 was alleviated when MPP+ was co-administered with rapamycin. Taken together, our results suggest that miR-7 and miR-153 protect neurons from cell death by interfering with the MPP+-induced downregulation of mTOR signaling.
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spelling doaj.art-b12675a45ffe47d5b68ec365ce2476fe2022-12-21T18:22:15ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-07-01810.3389/fncel.2014.0018267587miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathwayApostolia eFragkouli0Epaminondas eDoxakis1Biomedical Research Foundation, Academy of AthensBiomedical Research Foundation, Academy of AthensDifferential expression of microRNAs (miRs) in the brain of patients with neurodegenerative diseases suggests that they may have key regulatory roles in the development of these disorders. Two such miRs, miR-7 and miR-153 have recently been shown to target α-synuclein, a protein critically involved in the pathological process of Parkinson’s disease. By using a well-established in culture Parkinson’s disease model that of neurotoxin 1-Methyl-4-Phenyl-Pyridinium (MPP+), we examined whether miR-7 and miR-153 display neuroprotective properties. Herein, we demonstrate that treatment of cortical neurons with MPP+ induced a dose-dependent cell death with apoptotic characteristics. This was reflected in altered intracellular signaling characterized by increased levels of activated kinases p38MAPK and ERK1/2 and reduced levels of activated AKT, p70S6K and SAPK/JNK. Overexpression of miR-7 or miR-153 by adenoviral transduction protected cortical neurons from MPP+-induced toxicity, restored neuronal viability and anti-apoptotic BCL-2 protein levels while attenuated activation of caspase-3. Moreover, both miR-7 and miR-153 interfered with MPP+-induced alterations in intracellular signaling pathways in a partially overlapping manner; specifically, they preserved activation of mTOR and SAPK/JNK signaling pathways in the MPP+-treated neurons, while miR-153 also attenuated MPP+-induced activation of p38MAPK. No major effects were observed in the rest of signaling cascades or proteins investigated. Furthermore, the neuroprotective effect of miR-7 and miR-153 was alleviated when MPP+ was co-administered with rapamycin. Taken together, our results suggest that miR-7 and miR-153 protect neurons from cell death by interfering with the MPP+-induced downregulation of mTOR signaling.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00182/fullNeuronsParkinson DiseaseNeuroprotectionBcl-2rapamycincaspase-3
spellingShingle Apostolia eFragkouli
Epaminondas eDoxakis
miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
Frontiers in Cellular Neuroscience
Neurons
Parkinson Disease
Neuroprotection
Bcl-2
rapamycin
caspase-3
title miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
title_full miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
title_fullStr miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
title_full_unstemmed miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
title_short miR-7 and miR-153 protect neurons against MPP+- induced cell death via upregulation of mTOR pathway
title_sort mir 7 and mir 153 protect neurons against mpp induced cell death via upregulation of mtor pathway
topic Neurons
Parkinson Disease
Neuroprotection
Bcl-2
rapamycin
caspase-3
url http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00182/full
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