Evidence map›Paper›PMID 32286307›Full record

ArticleNature communications2020

P2X7 receptor inhibition ameliorates dendritic spine pathology and social behavioral deficits in Rett syndrome mice.

Juan Mauricio Garré, Hernandez Moura Silva, Juan J Lafaille, Guang Yang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. 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
5.6field-weighted citation impact, top 4% 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, 42 citations in OpenAlex.

  1. Article
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  7. Neuronal connectivity, behavioral, and transcriptional alterations associated with the loss of MARK2.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
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  17. Analysis of P2X7-Induced Neuronal Branching.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  18. Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Juan Mauricio GarréDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, 10032, USA. jmg2340@cumc.columbia.edu.
Hernandez Moura SilvaKimmel Center for Biology and Medicine at the Skirball Institute, New York University School of Medicine, New York, NY, 10016, USA.
Juan J LafailleKimmel Center for Biology and Medicine at the Skirball Institute, New York University School of Medicine, New York, NY, 10016, USA.
Guang YangDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, 10032, USA. gy2268@cumc.columbia.edu.ORCID http://orcid.org/0000-0002-5739-9126
Columbia University Irving Medical Center · USNew York University · US

Funding

The roles of anesthetics and neuroimmune interactions in postoperative cognitive dysfunctionR35GM131765 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Guang Yang · 2019 to 2026
$3.4M
Long-lasting effects of anesthetics on synapse development and plasticityR01GM107469 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI YANG, GUANG · 2014 to 2018
$1.6M
NIGMS NIH HHS R01 GM107469NIGMS NIH HHS R35 GM131765
6 · The paper itself

Abstract

Dysregulated immunity has been implicated in the pathogenesis of neurodevelopmental disorders but its contribution to synaptic and behavioral deficits in Rett syndrome (RTT) remains unknown. P2X7 receptors (P2X7Rs) are unique purinergic receptors with pro-inflammatory functions. Here, we report in a MECP2-deficient mouse model of RTT that the border of the cerebral cortex exhibits increased number of inflammatory myeloid cells expressing cell-surface P2X7Rs. Total knockout of P2X7Rs in MECP2 deficient mice decreases the number of inflammatory myeloid cells, restores cortical dendritic spine dynamics, and improves the animals' neurological function and social behavior. Furthermore, either genetic depletion of P2X7Rs in bone-marrow derived leukocytes or pharmacological block of P2X7Rs primarily outside of the central nervous system parenchyma, recapitulates the beneficial effects of total P2X7R depletion on the social behavior. Together, our results highlight the pathophysiological roles of P2X7Rs in a mouse model of RTT.

Indexed as

AnimalsBrainDendritic SpinesDisease Models, AnimalFlow CytometryMaleMiceMice, KnockoutPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7Rett SyndromeRosaniline Dyescoomassie Brilliant BluePurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7Rosaniline Dyes

Identifiers

PMID32286307
PMCPMC7156443
OpenAlexW3015207228

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.