Evidence map›Paper›PMID 24646437›Full record

ArticleThe European journal of neuroscience2014

Activity-dependent regulation of release probability at excitatory hippocampal synapses: a crucial role of fragile X mental retardation protein in neurotransmission.

Xiao-Sheng Wang, Chun-Zi Peng, Wei-Jun Cai, Jian Xia, Daozhong Jin, Yuqiao Dai, Xue-Gang Luo, Vitaly A Klyachko, Pan-Yue Deng

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. FMRP Sustains Presynaptic Function via Control of Activity-Dependent Bulk Endocytosis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Functional Deficiencies in Fragile X Neurons Derived from Human Embryonic Stem Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Article
  13. Article
  14. Impaired presynaptic long-term potentiation in the anterior cingulate cortex of Fmr1 knock-out mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  15. Review
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 4 institutions in 2 countries.

Xiao-Sheng WangDepartment of Histology and Embryology, Department of Anatomy and Neurobiology, Xiangya School of Medicine, Central South University, Changsha 410013, China.
Chun-Zi Peng
Wei-Jun Cai
Jian Xia
Daozhong Jin
Yuqiao Dai
Xue-Gang Luo
Vitaly A Klyachko
Pan-Yue Deng
Central South University · CNWashington University in St. Louis · USUniversity of Missouri–Kansas City · USXiangya Hospital Central South University · CN

Funding

MULTIPLE ROLES OF FMRP IN SYNAPTIC FUNCTION AND PLASTICITYR01NS081972 · NINDS · WASHINGTON UNIVERSITY · PI KLYACHKO, VITALY A · 2012 to 2016
$1.7M
NINDS NIH HHS R01 NS081972
6 · The paper itself

Abstract

Transcriptional silencing of the Fmr1 gene encoding fragile X mental retardation protein (FMRP) causes fragile X syndrome (FXS), the most common form of inherited intellectual disability and the leading genetic cause of autism. FMRP has been suggested to play important roles in regulating neurotransmission and short-term synaptic plasticity at excitatory hippocampal and cortical synapses. However, the origins and mechanisms of these FMRP actions remain incompletely understood, and the role of FMRP in regulating synaptic release probability and presynaptic function remains debated. Here we used variance-mean analysis and peak-scaled nonstationary variance analysis to examine changes in both presynaptic and postsynaptic parameters during repetitive activity at excitatory CA3-CA1 hippocampal synapses in a mouse model of FXS. Our analyses revealed that loss of FMRP did not affect the basal release probability or basal synaptic transmission, but caused an abnormally elevated release probability specifically during repetitive activity. These abnormalities were not accompanied by changes in excitatory postsynaptic current kinetics, quantal size or postsynaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor conductance. Our results thus indicate that FMRP regulates neurotransmission at excitatory hippocampal synapses specifically during repetitive activity via modulation of release probability in a presynaptic manner. Our study suggests that FMRP function in regulating neurotransmitter release is an activity-dependent phenomenon that may contribute to the pathophysiology of FXS.

Indexed as

Synaptic TransmissionAnimalsCA1 Region, HippocampalCA3 Region, HippocampalDisease Models, AnimalExcitatory Postsynaptic PotentialsFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeKineticsMaleMice, KnockoutPatch-Clamp TechniquesPresynaptic TerminalsPyramidal CellsReceptors, AMPAFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Receptors, AMPAexcitatory postsynaptic currentfragile X syndromehippocampusmouserelease probabilityshort-term plasticity

Identifiers

PMID24646437
PMCPMC4028396
OpenAlexW2115534144

What OpenQuestion holds

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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 OpenQuestion graph.