Evidence map›Paper›PMID 28857161›Full record

ArticleThe Journal of comparative neurology2017

Structural and functional differences in the barrel cortex of Mecp2 null mice.

Li-Jen Lee, Vassiliy Tsytsarev, Reha S Erzurumlu

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. X-Linked Epilepsies: A Narrative Review.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Clinical and Preclinical Evidence for MNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Article
  10. Multimodal Neuroimaging in Rett Syndrome WithFrontiers in neurology · 2022
    Review
  11. Extracellular Vesicles in CNS Developmental Disorders.International journal of molecular sciences · 2020
    Review
  12. How the Barrel Cortex Became a Working Model for Developmental Plasticity: A Historical Perspective.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. Article
  14. Review
  15. Rett Syndrome and CDKL5 Deficiency Disorder: From Bench to Clinic.International journal of molecular sciences · 2019
    Review
  16. 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

3 authors at 1 institution in 2 countries.

Li-Jen LeeGraduate Institute of Anatomy and Cell Biology, National Taiwan University, Taipei, Taiwan, ROC.
Vassiliy TsytsarevDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland.
Reha S ErzurumluDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland.ORCID http://orcid.org/0000-0003-1158-1771
University of Maryland, Baltimore · US

Funding

Thalamocortical circuit defects in developmental brain disordersR01NS092216 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2015 to 2019
$2.9M
NINDS NIH HHS R01 NS092216
6 · The paper itself

Abstract

Functional deficits in sensory systems are commonly noted in neurodevelopmental disorders, such as the Rett syndrome (RTT). Defects in methyl CpG binding protein gene (MECP2) largely accounts for RTT. Manipulations of the Mecp2 gene in mice provide useful models to probe into various aspects of brain development associated with the RTT. In this study, we focused on the somatosensory cortical phenotype in the Bird mouse model of RTT. We used voltage-sensitive dye imaging to evaluate whisker sensory evoked activity in the barrel cortex of mice. We coupled this functional assay with morphological analyses in postnatal mice and investigated the dendritic differentiation of barrel neurons and individual thalamocortical axon (TCA) arbors that synapse with them. We show that in Mecp2-deficient male mice, whisker-evoked activity is roughly topographic but weak in the barrel cortex. At the morphological level, we find that TCA arbors fail to develop into discrete, concentrated patches in barrel hollows, and the complexity of the dendritic branches in layer IV spiny stellate neurons is reduced. Collectively, our results indicate significant structural and functional impairments in the barrel cortex of the Bird mouse line, a popular animal model for the RTT. Such structural and functional anomalies in the primary somatosensory cortex may underlie orofacial tactile sensitivity issues and sensorimotor stereotypies characteristic of RTT.

Indexed as

Afferent PathwaysAnimalsCarbocyaninesDendritesDisease Models, AnimalMaleMethyl-CpG-Binding Protein 2MiceMice, Inbred C57BLMice, TransgenicNeuronsRett SyndromeSilver StainingSomatosensory CortexVibrissaeVoltage-Sensitive Dye ImagingCarbocyaninesMecp2 protein, mouseMethyl-CpG-Binding Protein 2axonbarrel cortexdendriteneural activityRett syndromeRRID: IMSR_JAX:000664RRID: MGI:3817236voltage-sensitive dye imaging

Identifiers

PMID28857161
PMCPMC5994756
OpenAlexW2750774138

What OpenQuestion holds

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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.