Evidence map›Paper›PMID 40666282›Full record

ArticleAmerican journal of clinical and experimental urology2025

Comparative transcriptome profiling of the lumbosacral dorsal root ganglia reveals sexually dimorphic gene expression in a murine model of coronavirus-induced neurodegeneration.

Taylor C Foley, Sathish K Yesupatham, Jake Miller-Dawson, Anna P Malykhina

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Article in American journal of clinical and experimental urology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Taylor C FoleyDivision of Urology, Department of Surgery, University of Colorado Anschutz Medical Campus Aurora, CO, USA.
Sathish K YesupathamDivision of Urology, Department of Surgery, University of Colorado Anschutz Medical Campus Aurora, CO, USA.
Jake Miller-DawsonDivision of Urology, Department of Surgery, University of Colorado Anschutz Medical Campus Aurora, CO, USA.
Anna P MalykhinaDivision of Urology, Department of Surgery, University of Colorado Anschutz Medical Campus Aurora, CO, USA.

Funding

Mechanisms of neurogenic bladder dysfunction in a viral murine model of multiple sclerosisR01DK116648 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MALYKHINA, ANNA P · 2020 to 2022
$1.0M
NIDDK NIH HHS R01 DK116648
6 · The paper itself

Abstract

introductionNeuroinflammation of the central nervous system (CNS) triggers long-lasting neurodegenerative changes associated with the development of neurogenic dysfunction in the pelvic organs. We previously described the symptoms of voiding dysfunction in a mouse model of multiple sclerosis (MS) induced by a coronaviral infection with mouse hepatitis virus (MHV). The aim of the current study was to identify immune, inflammatory and neuronal changes in the lumbosacral (L6-S2) dorsal root ganglia (DRG) innervating the lower urinary tract (LUT) after severe neurodegeneration in the CNS.

methodsAdult C57BL/6 male (N=18) and female (N=18) mice received either an intracranial injection of MHV (coronavirus-induced encephalomyelitis, CIE group), or sterile saline (control group). Dorsal root ganglia were collected from mice of both sexes at 1 and 4 weeks, followed by isolation of total RNA and bulk RNA sequencing.

resultsTranscriptome analysis of LS DRG identified a sex dependent expression of the genes at baseline with females having an increased expression of the immune system and extracellular matrix (ECM) related differentially expressed genes (DEGs) whereas males showed an upregulation of the genes belonging to protein synthesis, folding, and post-translational phosphorylation. Acute neuroinflammation (1 wk post-infection) triggered extensive immune responses involving the families of interferons (

conclusionsThis study confirmed a differential expression of immune, inflammatory, and neural DEGs in sensory ganglia of male and female mice undergoing CNS neurodegeneration and neuroinflammation. The obtained results suggest a functional role of sex-dependent sensory interoception in the development of neurogenic LUTS in a coronavirus-induced murine model of MS.

Indexed as

bulk RNAseqlower urinary tractneurodegenerationneurogenic LUTSSensory ganglia

Identifiers

PMID40666282
PMCPMC12256358

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