Evidence map›Paper›PMID 37034711›Full record

ArticlebioRxiv : the preprint server for biology2023

Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology.

Victoria Sook Keng Tung, Fasil Mathews, Marina Boruk, Gabrielle Suppa, Robert Foronjy, Michele Pato, Carlos Pato, James A Knowles, Oleg V Evgrafov

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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
–field-weighted citation impact
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

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Victoria Sook Keng TungDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY, USA.
Fasil MathewsDepartment of Otolaryngology, State University of New York at Downstate, Brooklyn, NY, USA.
Marina BorukDepartment of Otolaryngology, State University of New York at Downstate, Brooklyn, NY, USA.
Gabrielle SuppaDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY, USA.
Robert ForonjyDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY, USA.
Michele PatoDepartment of Psychiatry, Rutgers University.
Carlos PatoDepartment of Psychiatry, Rutgers University.
James A KnowlesHuman Genetics Institute of New Jersey, Rutgers University, Piscataway, NJ, USA.
Oleg V EvgrafovDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY, USA.
State University of New York · USRutgers Sexual and Reproductive Health and Rights · NLRutgers, The State University of New Jersey · US

Funding

African Ancestry Genomic Psychiatry CohortR01MH104964 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI BIGDELI, TIM BERNARD, FANOUS, AYMAN H · 2015 to 2024
$16.7M
Latino Ancestry Genomic Psychiatry CohortR01MH123451 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI BIGDELI, TIM BERNARD, FANOUS, AYMAN H · 2020 to 2025
$7.1M
TRANSCRIPTOME SEQUENCING OF NEURONAL CELL LINES FROM PATIENTS WITH SCHIZOPHRENIAR01MH086874 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI EVGRAFOV, OLEG V · 2011 to 2015
$3.4M
NIMH NIH HHS R01 MH086874NIMH NIH HHS R01 MH104964NIMH NIH HHS R01 MH123451
6 · The paper itself

Abstract

Study of the neurodevelopmental molecular mechanisms of schizophrenia requires the development of adequate biological models such as patient-derived cells and their derivatives. We previously used cell lines with neural progenitor properties (CNON) derived from superior or middle turbinates of patients with schizophrenia and control groups to study gene expression specific to schizophrenia. In this study, we compared single cell-RNA seq data from two CNON cell lines, one derived from an individual with schizophrenia (SCZ) and the other from a control group, with two biopsy samples from the middle turbinate (MT), also from an individual with SCZ and a control. In addition, we compared our data with previously published data from olfactory neuroepithelium (1). Our data demonstrated that CNON originated from a single cell type which is present both in middle turbinate and olfactory neuroepithelium. CNON express multiple markers of mesenchymal cells. In order to define relatedness of CNON to the developing human brain, we also compared CNON datasets with scRNA-seq data of embryonic brain (2) and found that the expression profile of CNON very closely matched one of the cell types in the embryonic brain. Finally, we evaluated differences between SCZ and control samples to assess usability and potential benefits of using single cell RNA-seq of CNON to study etiology of schizophrenia.

Indexed as

mesenchymal cellsmiddle turbinateneural progenitorsschizophreniascRNA-seq

Identifiers

PMID37034711
PMCPMC10081251
OpenAlexW4361294804

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.