Evidence map›Paper›PMID 37895019›Full record

ArticleInternational journal of molecular sciences2023

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 T Pato, Carlos N Pato, James A Knowles, Oleg V Evgrafov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Victoria Sook Keng TungDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.ORCID 0009-0007-5650-897X
Fasil MathewsDepartment of Otolaryngology, State University of New York at Downstate, Brooklyn, NY 11203, USA.
Marina BorukDepartment of Otolaryngology, State University of New York at Downstate, Brooklyn, NY 11203, USA.
Gabrielle SuppaDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.
Robert ForonjyDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.
Michele T PatoDepartment of Psychiatry, Rutgers University, Piscataway, NJ 08854, USA.
Carlos N PatoDepartment of Psychiatry, Rutgers University, Piscataway, NJ 08854, USA.
James A KnowlesHuman Genetics Institute of New Jersey, Rutgers University, Piscataway, NJ 08854, USA.
Oleg V EvgrafovDepartment of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.ORCID 0000-0003-0167-3939
State University of New York · USRutgers, The State University of New Jersey · US

Funding

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 Grant MH086874NIMH NIH HHS R01 MH086874
6 · The paper itself

Abstract

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

Indexed as

Neural Stem CellsSchizophreniaCells, CulturedHumansNeuronsTurbinatesmesenchymal cellsmiddle turbinateneurodevelopmentschizophreniascRNA-seq

Identifiers

PMID37895019
PMCPMC10607243
OpenAlexW4387777160

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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.