Proteomics

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LC-MS/MS analysis of proteomic changes in the spinal cord during experimental autoimmune encephalomyelitis


ABSTRACT: Experimental autoimmune encephalomyelitis (EAE) is a key model of autoimmune neuroinflammation, yet an integrated characterization of transcriptional dysregulation in the central nervous system has been limited. In this study, we performed proteomic profiling of dysregulated gene expression in the spinal cord of female and male C57BL/6JRccHsd mice induced with EAE during the acute disease phase using TMT LC-MS/MS. The associated transcriptomics dataset (RNA-sequencing analysis of transcriptomic changes in the spinal cord during experimental autoimmune encephalomyelitis) can be found on GEO. We identified extensive upregulation of innate and adaptive immune response signatures alongside downregulation of neuronal, synaptic, and mitochondrial pathways at the transcript level. Comparative analyses revealed broad pathway‑level changes associated with neuroinflammation, while highlighting limitations of transcriptomics alone in capturing alterations related to synaptic and metabolic integrity. This dataset provides a resource for investigating molecular remodeling of the inflamed central nervous system during autoimmune neuroinflammation.

INSTRUMENT(S):

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Spinal Cord

SUBMITTER: Elena Prepoudis  

LAB HEAD: Elizaveta Solovyeva

PROVIDER: PXD078146 | Pride | 2026-07-13

REPOSITORIES: Pride

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Integrated proteogenomic profiling reveals coordinated differential expression signatures during neuroinflammation.

Prepoudis Elena E   Pfister Sabina S   Hofmann Andreas A   Altorfer Marc M   Catalano Marco M   Sindelar Miriam M   Ramseier Pamela P   Lafossas Frédérique F   Tisserand Sarah S   Junt Tobias T   Schubart Anna A   Locatelli Giuseppe G   Solovyeva Elizaveta E  

Acta neuropathologica communications 20260710


<h4>Background</h4>Experimental autoimmune encephalomyelitis (EAE) is a key model of autoimmune neuroinflammation, yet an integrated characterization of transcriptional and proteomic dysregulation of the CNS has been missing.<h4>Methods</h4>In this study, we performed deep proteogenomic profiling of the spinal cord from mice induced with EAE during acute disease by combining RNA-seq (GEO, GSE330115) and LC-MS/MS (PRIDE, PXD078146).<h4>Results</h4>We identified extensive upregulation of innate an  ...[more]

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