Language

English

Publication Date

11-1-2026

Journal

Glia

DOI

10.1002/glia.70230

PMID

42760594

PMCID

PMC13589049

PubMedCentral® Posted Date

9-18-2026

PubMedCentral® Full Text Version

Post-print

Abstract

Pediatric obstructive sleep apnea (POSA) is a common childhood disease that often causes aberrant brain development and cognitive deficits. The pathophysiological underpinnings of cognitive impairments in POSA remain unclear. Here, we examined cellular and molecular aspects of pathology in a mouse model of POSA that features learning and memory deficits. We performed single-nucleus RNA-sequencing (snRNA-seq) of the hippocampus to examine gene expression changes in an unbiased and cell type-specific manner. This dataset revealed a striking perturbation of transcriptomes across all brain cell types, particularly within glia and neural stem cells. We validated reduced expression of several differentially expressed genes at protein level: QDPR and SOX8 in oligodendrocytes, LRRK2 and NDUFS4 in neural stem cells, TFE3 in microglia, and GLUT1 in astrocytes. Comparison of oligodendrocyte gene expression changes with proteomic datasets suggested impairments in myelination, which we confirmed in vivo. Furthermore, cellular level analyses demonstrated aberrant morphology of oligodendrocytes, astrocytes, and microglia in the hippocampus, and diminished numbers of neural stem cells in the subgranular zone. Our study identifies cellular and molecular glial cell dysfunction in POSA, validates gene targets for further study, and provides an snRNA-seq dataset to facilitate further data-driven hypothesis generation.

Keywords

Animals, Memory Disorders, Disease Models, Animal, Mice, Neuroglia, Sleep Apnea, Obstructive, Hippocampus, Male, Mice, Inbred C57BL, Neural Stem Cells, Oligodendroglia, astrocyte, cognition, glia, microglia, neurogenesis, oligodendrocyte, sleep apnea

Published Open-Access

yes

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