Evidence map›Paper›PMID 35794118›Full record

ArticleNature communications2022

Pattern decorrelation in the mouse medial prefrontal cortex enables social preference and requires MeCP2.

Pan Xu, Yuanlei Yue, Juntao Su, Xiaoqian Sun, Hongfei Du, Zhichao Liu, Rahul Simha, Jianhui Zhou, Chen Zeng, Hui Lu

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  14. Dopamine D1 receptor in medial prefrontal cortex mediates the effects of TAAR1 activation on chronic stress-induced cognitive and social deficits.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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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

10 authors at 3 institutions in 2 countries.

Pan Xu *The GW Institute for Neuroscience, The George Washington University, Washington, DC, 20037, USA.
Yuanlei Yue *The GW Institute for Neuroscience, The George Washington University, Washington, DC, 20037, USA.ORCID 0000-0002-0552-2911
Juntao SuThe GW Institute for Neuroscience, The George Washington University, Washington, DC, 20037, USA.
Xiaoqian SunDepartment of Computer Science, School of Engineering and Applied Science, The George Washington University, Washington, DC, 20037, USA.
Hongfei DuDepartment of Statistics, Columbian College of Art and Sciences, The George Washington University, Washington, DC, 20037, USA.ORCID 0000-0002-0633-594X
Zhichao LiuDepartment of Physics, Columbian College of Art and Sciences, The George Washington University, Washington, DC, 20037, USA.ORCID 0000-0002-9274-7229
Rahul SimhaDepartment of Computer Science, School of Engineering and Applied Science, The George Washington University, Washington, DC, 20037, USA.
Jianhui ZhouDepartment of Statistics, School of Arts and Sciences, University of Virginia, Charlottesville, VA, 22904, USA.
Chen ZengDepartment of Statistics, Columbian College of Art and Sciences, The George Washington University, Washington, DC, 20037, USA.ORCID 0000-0001-7778-6388
Hui LuThe GW Institute for Neuroscience, The George Washington University, Washington, DC, 20037, USA. huilu@email.gwu.edu.ORCID 0000-0003-2336-2170
George Washington University · USChongqing University of Posts and Telecommunications · CNUniversity of Virginia · US

Funding

Understanding the effects of motor learning in wild-type and Mecp2-deficient miceR01NS118197 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI Hui Lu · 2022 to 2026
$2.3M
Mechanisms and rescue of neural circuit dysfunction in Mecp2 mutant miceR00NS089824 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI LU, HUI · 2017 to 2019
$747k
NINDS NIH HHS R00 NS089824NINDS NIH HHS R01 NS118197
6 · The paper itself

Abstract

Sociability is crucial for survival, whereas social avoidance is a feature of disorders such as Rett syndrome, which is caused by loss-of-function mutations in MECP2. To understand how a preference for social interactions is encoded, we used in vivo calcium imaging to compare medial prefrontal cortex (mPFC) activity in female wild-type and Mecp2-heterozygous mice during three-chamber tests. We found that mPFC pyramidal neurons in Mecp2-deficient mice are hypo-responsive to both social and nonsocial stimuli. Hypothesizing that this limited dynamic range restricts the circuit's ability to disambiguate coactivity patterns for different stimuli, we suppressed the mPFC in wild-type mice and found that this eliminated both pattern decorrelation and social preference. Conversely, stimulating the mPFC in MeCP2-deficient mice restored social preference, but only if it was sufficient to restore pattern decorrelation. A loss of social preference could thus indicate impaired pattern decorrelation rather than true social avoidance.

Indexed as

Methyl-CpG-Binding Protein 2Rett SyndromeSocial BehaviorAnimalsFemaleMicePrefrontal CortexPyramidal CellsSocial Behavior DisordersMecp2 protein, mouseMethyl-CpG-Binding Protein 2

Identifiers

PMID35794118
PMCPMC9259602
OpenAlexW4284891355

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.