Perturbation of Cell-subtype specific Active Kinome Networks in Schizophrenia

Schizophrenia is a serious illness with significant effects on patients and their families. Because the disease impacts executive function, the Dorsolateral Prefrontal Cortex (DLPFC) has been a focus of study. We previously reported altered protein kinase activity, including AKT, in postmortem brain samples from patients with schizophrenia. Now, we extend this research to the cellular level, concentrating on frontal cortical pyramidal neurons. Using laser capture microdissection, we isolated DLPFC pyramidal neurons from matched pairs of schizophrenia and control postmortem brain samples (n = 20 per group). We then used the PamChip STK kinome array assay for high-throughput analysis of kinase activity. With well-established bioinformatics methods, we identified upstream kinases involved in schizophrenia. Several kinases of interest emerged, such as c-Jun N-terminal kinases (JNK), extracellular signal-regulated kinases (ERK), and p38 mitogen-activated protein kinases (P38). Of these, the P38 kinases were of particular importance as they are involved in the inflammation cascade and immune function. Next, we applied a new technique to identify kinase interaction networks within high-throughput kinase activity data. This modeling enabled us to detect network-level changes in pyramidal neurons in schizophrenia. This is the first study to analyze the subkinome at the cellular level in schizophrenia and to reveal active kinome network changes in this often-devastating illness. Prevailing hypotheses regarding the etiology of schizophrenia include aberrant synapse turnover, which is mediated by microglia and immune function pathways. Our findings offer a crucial new starting point for understanding how disrupted signaling networks may mediate the pathophysiology of this often devastating severe mental illness.

Institutions

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-09-26
DOI
https://doi.org/10.5281/zenodo.17334341
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Perturbation of Cell-subtype specific Active Kinome Networks in Schizophrenia

Zenodo (CERN European Organization for Nuclear Research)
Bacteriophages and microbial interactions
article

Perturbation of Cell-subtype specific Active Kinome Networks in Schizophrenia

article en

Abstract

Schizophrenia is a serious illness with significant effects on patients and their families. Because the disease impacts executive function, the Dorsolateral Prefrontal Cortex (DLPFC) has been a focus of study. We previously reported altered protein kinase activity, including AKT, in postmortem brain samples from patients with schizophrenia. Now, we extend this research to the cellular level, concentrating on frontal cortical pyramidal neurons. Using laser capture microdissection, we isolated DLPFC pyramidal neurons from matched pairs of schizophrenia and control postmortem brain samples (n = 20 per group). We then used the PamChip STK kinome array assay for high-throughput analysis of kinase activity. With well-established bioinformatics methods, we identified upstream kinases involved in schizophrenia. Several kinases of interest emerged, such as c-Jun N-terminal kinases (JNK), extracellular signal-regulated kinases (ERK), and p38 mitogen-activated protein kinases (P38). Of these, the P38 kinases were of particular importance as they are involved in the inflammation cascade and immune function. Next, we applied a new technique to identify kinase interaction networks within high-throughput kinase activity data. This modeling enabled us to detect network-level changes in pyramidal neurons in schizophrenia. This is the first study to analyze the subkinome at the cellular level in schizophrenia and to reveal active kinome network changes in this often-devastating illness. Prevailing hypotheses regarding the etiology of schizophrenia include aberrant synapse turnover, which is mediated by microglia and immune function pathways. Our findings offer a crucial new starting point for understanding how disrupted signaling networks may mediate the pathophysiology of this often devastating severe mental illness.

Zenodo (CERN European Organization for Nuclear Research)
University of Toledo Medical Center (US), Cincinnati Children's Hospital Medical Center (US), Emory University (US), University of California San Diego (US), The Ohio State University (US), University of Cincinnati (US), University of Toledo (US), Des Moines University (US)
Openalex Percentile: Top 39%
Bacteriophages and microbial interactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.