Evidence map›Paper›PMID 38203282›Full record

ReviewInternational journal of molecular sciences2023

Molecular Mechanisms of AMPA Receptor Trafficking in the Nervous System.

Yi-Yang Cao, Ling-Ling Wu, Xiao-Nan Li, Yu-Lian Yuan, Wan-Wei Zhao, Jing-Xuan Qi, Xu-Yu Zhao, Natalie Ward, Jiao Wang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  4. Neuronal Calcium Signaling and Cytoskeletal Dynamics in Neurodegeneration.International journal of molecular sciences · 2026
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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 2 institutions in 2 countries.

Yi-Yang CaoLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Ling-Ling WuSchool of Medicine, Shanghai University, Shanghai 200444, China.
Xiao-Nan LiLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Yu-Lian YuanLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Wan-Wei ZhaoLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Jing-Xuan QiLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Xu-Yu ZhaoLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Natalie WardMedical Laboratory, Exceptional Community Hospital, 19060 N John Wayne Pkwy, Maricopa, AZ 85139, USA.
Jiao WangLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.ORCID 0000-0001-9875-5425
Shanghai University · CNCommunity Hospital · US

Funding

the Basic Research Program of Shanghai 20JC1412200the National Key Research and Development Program of China 2018YFA0109800the National Key Research and Development Program of China 2020YFA0113000the National Natural Science Foundation of China 81971324 and 31500827
6 · The paper itself

Abstract

Synaptic plasticity enhances or reduces connections between neurons, affecting learning and memory. Postsynaptic AMPARs mediate greater than 90% of the rapid excitatory synaptic transmission in glutamatergic neurons. The number and subunit composition of AMPARs are fundamental to synaptic plasticity and the formation of entire neural networks. Accordingly, the insertion and functionalization of AMPARs at the postsynaptic membrane have become a core issue related to neural circuit formation and information processing in the central nervous system. In this review, we summarize current knowledge regarding the related mechanisms of AMPAR expression and trafficking. The proteins related to AMPAR trafficking are discussed in detail, including vesicle-related proteins, cytoskeletal proteins, synaptic proteins, and protein kinases. Furthermore, significant emphasis was placed on the pivotal role of the actin cytoskeleton, which spans throughout the entire transport process in AMPAR transport, indicating that the actin cytoskeleton may serve as a fundamental basis for AMPAR trafficking. Additionally, we summarize the proteases involved in AMPAR post-translational modifications. Moreover, we provide an overview of AMPAR transport and localization to the postsynaptic membrane. Understanding the assembly, trafficking, and dynamic synaptic expression mechanisms of AMPAR may provide valuable insights into the cognitive decline associated with neurodegenerative diseases.

Indexed as

Central Nervous System DepressantsReceptors, AMPACentral Nervous SystemCognitionLearningNeuronsCentral Nervous System DepressantsReceptors, AMPAAMPARAMPAR traffickingglutamate receptorsmolecular mechanismsynaptic plasticity

Identifiers

PMID38203282
PMCPMC10779435
OpenAlexW4390054866

What OpenQuestion 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 OpenQuestion graph.