Evidence map›Paper›PMID 21605958›Full record

ArticleSchizophrenia research2011

Expression of mutant human DISC1 in mice supports abnormalities in differentiation of oligodendrocytes.

Pavel Katsel, Weilun Tan, Bagrat Abazyan, Kenneth L Davis, Christopher Ross, Mikhail V Pletnikov, Vahram Haroutunian

Open access · greenAbstract read
In one paragraph

Article in Schizophrenia research, 2011. 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
1.7field-weighted citation impact, top 17% 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, 40 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Pavel KatselDepartment of Psychiatry, The Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029-6575, USA. pavel.katsel@mssm.edu
Weilun Tan
Bagrat Abazyan
Kenneth L Davis
Christopher Ross
Mikhail V Pletnikov
Vahram Haroutunian
Icahn School of Medicine at Mount Sinai · USJohns Hopkins Medicine · USJohns Hopkins University · USMount Sinai Hospital · US

Funding

White Matter Abnormalities in SchizophreniaP50MH066392 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BUXBAUM, JOSEPH D. · 2002 to 2012
$18.6M
Mutant DISC 1 and Abnormal Neurodevelopment in Mental IllnessR01MH083728 · NIMH · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI PLETNIKOV, MIKHAIL V · 2009 to 2020
$4.9M
Cortico-thalamic Glutamate/GABA mRNA in schizophreniaR01MH064673 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI HAROUTUNIAN, VAHRAM · 2003 to 2012
$3.4M
Inducible expression of mutant DISC1: transgenic mouse modelR21MH077792 · NIMH · JOHNS HOPKINS UNIVERSITY · PI PLETNIKOV, MIKHAIL V · 2007 to 2008
$406k
Autism Speaks AS2574NIMH NIH HHS MH064673NIMH NIH HHS MH66392NIMH NIH HHS R01 MH064673NIMH NIH HHS R01 MH083728NIMH NIH HHS R21 MH077792
6 · The paper itself

Abstract

Abnormalities in oligodendrocyte (OLG) differentiation and OLG gene expression deficit have been described in schizophrenia (SZ). Recent studies revealed a critical requirement for Disrupted-in-Schizophrenia 1 (DISC1) in neural development. Transgenic mice with forebrain restricted expression of mutant human DISC1 (ΔhDISC1) are characterized by neuroanatomical and behavioral abnormalities reminiscent of some features of SZ. We sought to determine whether the expression of ΔhDISC1 may influence the development of OLGs in this mouse model. OLG- and cell cycle-associated gene and protein expression were characterized in the forebrain of ΔhDISC1 mice during different stages of neurodevelopment (E15 and P1 days) and in adulthood. The results suggest that the expression of ΔhDISC1 exerts a significant influence on oligodendrocyte differentiation and function, evidenced by premature OLG differentiation and increased proliferation of their progenitors. Additional findings showed that neuregulin 1 and its receptors may be contributing factors to the observed upregulation of OLG genes. Thus, OLG function may be perturbed by mutant hDISC1 in a model system that provides new avenues for studying aspects of the pathogenesis of SZ.

Indexed as

AnimalsAnimals, NewbornBrainCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell Cycle ProteinsCell DifferentiationDoxycyclineEmbryo, MammalianFemaleGene Expression Regulation, DevelopmentalHumansMiceMice, TransgenicMutationMyelin-Associated GlycoproteinNerve Tissue ProteinsCalcium-Calmodulin-Dependent Protein Kinase Type 2CAMK2A protein, humanCell Cycle ProteinsDISC1 protein, humanDoxycyclineMyelin-Associated GlycoproteinNerve Tissue ProteinsPhosphoric Diester HydrolasesQk protein, mouseReceptor, Platelet-Derived Growth Factor alphaRNA-Binding ProteinsRNA, MessengerSox10 protein, mouseSOXE Transcription Factors

Identifiers

PMID21605958
PMCPMC3139741
OpenAlexW1969115687

What OpenQuestion holds

Textmetadata
LicenceTDM
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.