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miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline

Microribonucleic acids (miRNAs) play a pivotal role in numerous aspects of the nervous system and are increasingly recognized as key regulators in neurodegenerative diseases. This study hypothesized that miR-34c, a miRNA expressed in mammalian hippocampi whose expression level can alter the hippocam...

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Autores principales: Kao, Yu-Chia, Wang, I-Fang, Tsai, Kuen-Jer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121231/
https://www.ncbi.nlm.nih.gov/pubmed/30096777
http://dx.doi.org/10.3390/ijms19082323
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author Kao, Yu-Chia
Wang, I-Fang
Tsai, Kuen-Jer
author_facet Kao, Yu-Chia
Wang, I-Fang
Tsai, Kuen-Jer
author_sort Kao, Yu-Chia
collection PubMed
description Microribonucleic acids (miRNAs) play a pivotal role in numerous aspects of the nervous system and are increasingly recognized as key regulators in neurodegenerative diseases. This study hypothesized that miR-34c, a miRNA expressed in mammalian hippocampi whose expression level can alter the hippocampal dendritic spine density, could induce memory impairment akin to that of patients with Alzheimer’s disease (AD) in mice. In this study, we showed that miR-34c overexpression in hippocampal neurons negatively regulated dendritic length and spine density. Hippocampal neurons transfected with miR-34c had shorter dendrites on average and fewer filopodia and spines than those not transfected with miR-34c (control mice). Because dendrites and synapses are key sites for signal transduction and fundamental structures for memory formation and storage, disrupted dendrites can contribute to AD. Therefore, we supposed that miR-34c, through its effects on dendritic spine density, influences synaptic plasticity and plays a key role in AD pathogenesis.
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spelling pubmed-61212312018-09-07 miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline Kao, Yu-Chia Wang, I-Fang Tsai, Kuen-Jer Int J Mol Sci Article Microribonucleic acids (miRNAs) play a pivotal role in numerous aspects of the nervous system and are increasingly recognized as key regulators in neurodegenerative diseases. This study hypothesized that miR-34c, a miRNA expressed in mammalian hippocampi whose expression level can alter the hippocampal dendritic spine density, could induce memory impairment akin to that of patients with Alzheimer’s disease (AD) in mice. In this study, we showed that miR-34c overexpression in hippocampal neurons negatively regulated dendritic length and spine density. Hippocampal neurons transfected with miR-34c had shorter dendrites on average and fewer filopodia and spines than those not transfected with miR-34c (control mice). Because dendrites and synapses are key sites for signal transduction and fundamental structures for memory formation and storage, disrupted dendrites can contribute to AD. Therefore, we supposed that miR-34c, through its effects on dendritic spine density, influences synaptic plasticity and plays a key role in AD pathogenesis. MDPI 2018-08-08 /pmc/articles/PMC6121231/ /pubmed/30096777 http://dx.doi.org/10.3390/ijms19082323 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kao, Yu-Chia
Wang, I-Fang
Tsai, Kuen-Jer
miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title_full miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title_fullStr miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title_full_unstemmed miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title_short miRNA-34c Overexpression Causes Dendritic Loss and Memory Decline
title_sort mirna-34c overexpression causes dendritic loss and memory decline
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121231/
https://www.ncbi.nlm.nih.gov/pubmed/30096777
http://dx.doi.org/10.3390/ijms19082323
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