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


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
19 Oct 2023
Historique:
received: 14 08 2023
revised: 02 10 2023
accepted: 10 10 2023
medline: 30 10 2023
pubmed: 28 10 2023
entrez: 28 10 2023
Statut: epublish

Résumé

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.

Identifiants

pubmed: 37895019
pii: ijms242015339
doi: 10.3390/ijms242015339
pmc: PMC10607243
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH086874
Pays : United States
Organisme : NIMH NIH HHS
ID : Grant MH086874
Pays : United States

Commentaires et corrections

Type : UpdateOf

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Auteurs

Victoria Sook Keng Tung (VSK)

Department of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.

Fasil Mathews (F)

Department of Otolaryngology, State University of New York at Downstate, Brooklyn, NY 11203, USA.

Marina Boruk (M)

Department of Otolaryngology, State University of New York at Downstate, Brooklyn, NY 11203, USA.

Gabrielle Suppa (G)

Department of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.

Robert Foronjy (R)

Department of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.

Michele T Pato (MT)

Department of Psychiatry, Rutgers University, Piscataway, NJ 08854, USA.

Carlos N Pato (CN)

Department of Psychiatry, Rutgers University, Piscataway, NJ 08854, USA.

James A Knowles (JA)

Human Genetics Institute of New Jersey, Rutgers University, Piscataway, NJ 08854, USA.

Oleg V Evgrafov (OV)

Department of Cell Biology, State University of New York at Downstate, Brooklyn, NY 11203, USA.
Human Genetics Institute of New Jersey, Rutgers University, Piscataway, NJ 08854, USA.

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