Evidence map›Paper›PMID 38493494›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

AFM Imaging Reveals MicroRNA-132 to be a Positive Regulator of Synaptic Functions.

Ikbum Park, Hyun Jin Kim, Juyoung Shin, Yu Jin Jung, Donggyu Lee, Ji-Seon Lim, Jong Mok Park, Joon Won Park, Joung-Hun Kim

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. AFM Imaging Reveals MicroRNA-132 to be a Positive Regulator of Synaptic Functions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Ikbum ParkTechnical Support Center for Chemical Industry, Korea Research Institute of Chemical Technology (KRICT), Ulsan, 44412, Republic of Korea.ORCID 0000-0003-3074-330X
Hyun Jin KimDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.ORCID 0000-0001-9108-151X
Juyoung ShinDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Yu Jin JungCenter for Specialty Chemicals, Korea Research Institute of Chemical Technology (KRICT), Ulsan, 44412, Republic of Korea.
Donggyu LeeDivision of Electronics and Information System, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Republic of Korea.
Ji-Seon LimDepartment of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Jong Mok ParkTechnical Support Center for Chemical Industry, Korea Research Institute of Chemical Technology (KRICT), Ulsan, 44412, Republic of Korea.
Joon Won ParkDepartment of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Joung-Hun KimDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.ORCID 0000-0001-6716-2037
Pohang University of Science and Technology · KRKorea Research Institute of Chemical Technology · KRDaegu Gyeongbuk Institute of Science and Technology · KR

Funding

Korea Research Institute of Chemical Technology KS2441-20National Research Foundation of Korea 2018R1A3B1052079National Research Foundation of Korea 2020R1C1C1007055National Research Foundation of Korea 2021R1I1A1A01044359National Research Foundation of Korea RS-2023-00245060National Research Foundation of Korea RS-2023-00265883
6 · The paper itself

Abstract

The modification of synaptic and neural connections in adults, including the formation and removal of synapses, depends on activity-dependent synaptic and structural plasticity. MicroRNAs (miRNAs) play crucial roles in regulating these changes by targeting specific genes and regulating their expression. The fact that somatic and dendritic activity in neurons often occurs asynchronously highlights the need for spatial and dynamic regulation of protein synthesis in specific milieu and cellular loci. MicroRNAs, which can show distinct patterns of enrichment, help to establish the localized distribution of plasticity-related proteins. The recent study using atomic force microscopy (AFM)-based nanoscale imaging reveals that the abundance of miRNA(miR)-134 is inversely correlated with the functional activity of dendritic spine structures. However, the miRNAs that are selectively upregulated in potentiated synapses, and which can thereby support prospective changes in synaptic efficacy, remain largely unknown. Using AFM force imaging, significant increases in miR-132 in the dendritic regions abutting functionally-active spines is discovered. This study provides evidence for miR-132 as a novel positive miRNA regulator residing in dendritic shafts, and also suggests that activity-dependent miRNAs localized in distinct sub-compartments of neurons play bi-directional roles in controlling synaptic transmission and synaptic plasticity.

Indexed as

MicroRNAsMicroscopy, Atomic ForceNeuronal PlasticitySynapsesAnimalsDendritic SpinesMiceMice, Inbred C57BLNeuronsMicroRNAsMIRN132 microRNA, mouseatomic force microscopydendritic spinesforce‐mappingmicroRNAsynaptic strengthening

Identifiers

PMID38493494
PMCPMC11077659
OpenAlexW4392892949

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.