Evidence map›Paper›PMID 36754912›Full record

ArticleMolecular neurobiology2023

Activity-Dependent Differential Regulation of Auts2 Isoforms In Vitro and In Vivo.

Wenbin Pang, Meijuan Wang, Qingshang Bi, Hongai Li, Qionglin Zhou, Xiaoshan Ye, Wei Xiang, Le Xiao

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 32% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Wenbin PangHainan Women and Children's Medical Center, Hainan Medical University, Haikou, China.
Meijuan WangSchool of Basic Medicine and Life Science, Hainan Medical University, Haikou, China.
Qingshang BiSchool of Basic Medicine and Life Science, Hainan Medical University, Haikou, China.
Hongai LiHainan Women and Children's Medical Center, Hainan Medical University, Haikou, China.
Qionglin ZhouSchool of Pediatrics, Hainan Medical University, Haikou, China.
Xiaoshan YeSchool of Pediatrics, Hainan Medical University, Haikou, China.
Wei XiangHainan Women and Children's Medical Center, Hainan Medical University, Haikou, China. 13907533529@163.com.
Le XiaoHainan Women and Children's Medical Center, Hainan Medical University, Haikou, China. Le.Xiao@hainmc.edu.cn.ORCID http://orcid.org/0000-0001-9703-1265
Hainan Medical University · CN

Funding

Hainan Graduate Students Innovation Projects Qhys2021-355Hainan Graduate Students Innovation Projects Qhys2021-357Hainan Provincial Department of Science and Technology ZDYF2020216Major Science and Technology Project of Hainan Province ZDKJ2019010National Natural Science Foundation of China No. 31960170Natural Science Foundation of Hainan Province 821QN1001the Excellent Talent Team of Hainan Province No.QRCBT202121the Hainan Province Clinical Medical Center QWYH202175
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder of unknown cause, although one hypothesis suggests a potential imbalance between excitation and inhibition that leads to changes in neuronal activity and a disturbance in the brain network. However, the mechanisms through which neuronal activity contributes to the development of ASD remain largely unexplained. In this study, we described that neuronal activity at the transcriptional and translational levels regulated the expression of Auts2 isoforms. The prolonged stimulation of cultured cortical neurons significantly reduced the auts2 transcripts, accompanied by the decrease of FL-Auts2 protein, as well as one of the short isoforms (S-Auts2 var.1). Blocking neuronal activity increased the number of auts2 transcripts but not protein levels. Furthermore, blocking the NMDA receptors during stimulation could partially restore the FL-Auts2 and S-Auts2 var.1 at protein level, but not at mRNA level. Finally, Auts2 expression in the hippocampus was reduced in mice exposed to an enriched environment, a behavior paradigm designed to increase the brain activity through abundant sensory and social stimulations. Thus, our study revealed a novel regulatory effect of neuronal activity on the transcription and translation of ASD-risk gene auts2.

Indexed as

Autism Spectrum DisorderCytoskeletal ProteinsAnimalsBrainMiceProtein IsoformsTranscription FactorsAuts2 protein, mouseCytoskeletal ProteinsProtein IsoformsTranscription FactorsActivity-dependent regulationAutism spectrum disorderAuts2

Identifiers

PMID36754912
OpenAlexW4319655808

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.