Your browser doesn't support javascript.
loading
Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia.
Evgrafov, Oleg V; Armoskus, Chris; Wrobel, Bozena B; Spitsyna, Valeria N; Souaiaia, Tade; Herstein, Jennifer S; Walker, Christopher P; Nguyen, Joseph D; Camarena, Adrian; Weitz, Jonathan R; Kim, Jae Mun Hugo; Lopez Duarte, Edder; Wang, Kai; Simpson, George M; Sobell, Janet L; Medeiros, Helena; Pato, Michele T; Pato, Carlos N; Knowles, James A.
Afiliación
  • Evgrafov OV; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York. Electronic address: oleg.evgrafov@downstate.edu.
  • Armoskus C; Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Wrobel BB; Caruso Department of Otolaryngology, Head and Neck Surgery, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Spitsyna VN; Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Souaiaia T; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York.
  • Herstein JS; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Walker CP; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Nguyen JD; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Camarena A; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Weitz JR; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Kim JMH; Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Lopez Duarte E; Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Wang K; Raymond G. Perelman Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Simpson GM; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Sobell JL; Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Medeiros H; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York.
  • Pato MT; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York.
  • Pato CN; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York.
  • Knowles JA; College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, New York.
Biol Psychiatry ; 88(3): 236-247, 2020 08 01.
Article en En | MEDLINE | ID: mdl-32143829
ABSTRACT

BACKGROUND:

Genome-wide association studies of schizophrenia have demonstrated that variations in noncoding regions are responsible for most of the common variation heritability of the disease. It is hypothesized that these risk variants alter gene expression. Therefore, studying alterations in gene expression in schizophrenia may provide a direct approach to understanding the etiology of the disease. In this study we use cultured neural progenitor cells derived from olfactory neuroepithelium (CNON cells) as a genetically unaltered cellular model to elucidate the neurodevelopmental aspects of schizophrenia.

METHODS:

We performed a gene expression study using RNA sequencing of CNON cells from 111 control subjects and 144 individuals with schizophrenia. Differentially expressed genes were identified with DESeq2 software, using covariates to correct for sex, age, library batches, and 1 surrogate variable component.

RESULTS:

A total of 80 genes were differentially expressed (false discovery rate < 10%), showing enrichment in cell migration, cell adhesion, developmental process, synapse assembly, cell proliferation, and related Gene Ontology categories. Cadherin and Wnt signaling pathways were positive in overrepresentation test, and, in addition, many genes were specifically involved in WNT5A signaling. The differentially expressed genes were modestly, but significantly, enriched in the genes overlapping single nucleotide polymorphisms with genome-wide significant association from the Psychiatric Genomics Consortium genome-wide association study of schizophrenia. We also found substantial overlap with genes associated with other psychiatric disorders or brain development, enrichment in the same Gene Ontology categories as genes with mutations de novo in schizophrenia, and studies of induced pluripotent stem cell-derived neural progenitor cells.

CONCLUSIONS:

CNON cells are a good model of the neurodevelopmental aspects of schizophrenia and can be used to elucidate the etiology of the disorder.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Células Madre Pluripotentes Inducidas / Células-Madre Neurales Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Biol Psychiatry Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Células Madre Pluripotentes Inducidas / Células-Madre Neurales Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Biol Psychiatry Año: 2020 Tipo del documento: Article
...