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Selective distribution and dynamic modulation of miRNAs in the synapse and its possible role in Alzheimer's Disease
Sylvia Garza-Manero1, Israel Pichardo-Casas2, Clorinda Arias1
1Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, CP 04510, México, DF, Mexico.
Abstract:
MicroRNAs (miRNAs) are small non-coding RNAs that control a wide range of functions in the cell. They act as post-transcriptional gene regulators throughout in development and in adulthood, although recent evidence suggests their potential role in the onset and development of various diseases and neuropathologies. In neurons miRNAs seem to play a key role as regulators of synaptic function. Synapses are vulnerable structures in neurodegenerative diseases. In particular, synaptic loss has been described as an early event in the pathogenesis of Alzheimer's Disease (AD). MicroRNA-mediated gene silencing represents a candidate event for the repression of specific mRNAs and protein synthesis that could account for synaptic dysfunction. In this work, we review the participation of miRNAs in synaptic function and consider their possible role in synaptic alterations in AD. First we review the biogenesis of miRNAs and their role as post-transcriptional regulators. Then we discuss recently published data on the distribution of miRNAs in the brain as well as their role in dynamic regulation at the synapse. In the second part, we briefly introduce the reader to AD, focusing on synaptic alterations in the progression of the pathology. Then we discuss possible implications of miRNAs in the associated synaptic dysfunction.
Insights
MicroRNAs (miRNAs) regulate gene expression and are crucial for neuronal function. This review explores their role in synaptic plasticity and potential involvement in Alzheimer's Disease (AD) pathogenesis.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression post-transcriptionally.
- Emerging evidence links miRNAs to disease onset and neuropathologies, particularly in neuronal function.
- Synaptic loss is an early hallmark of Alzheimer's Disease (AD) pathogenesis.
Purpose of the Study:
- To review the role of miRNAs in synaptic function.
- To explore the potential involvement of miRNAs in synaptic alterations observed in Alzheimer's Disease (AD).
Main Methods:
- Review of miRNA biogenesis and function as post-transcriptional regulators.
- Discussion of published data on miRNA distribution and synaptic regulation in the brain.
- Analysis of AD pathology with a focus on synaptic alterations.
Main Results:
- miRNAs are key regulators of synaptic function in neurons.
- MicroRNA-mediated gene silencing may contribute to synaptic dysfunction in neurodegenerative diseases.
- Synaptic alterations are central to AD progression, with miRNAs potentially playing a significant role.
Conclusions:
- miRNAs are critical for maintaining synaptic health.
- Dysregulation of miRNAs may underlie synaptic dysfunction in Alzheimer's Disease.
- Further research into miRNA's role in AD is warranted.
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