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Data · dataset · 2025

Single cell RNA-seq of young and aged whole lungs following IAV infection

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We report analysis of lung single cell transcriptome in aged and young mice infected with influenza A virus (IAV) for 9 days. It represents Cd4+ T cells population in aged lung were substantially decreased.

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Moreover mTOR signaling pathway were downregulated in Cd4+ cluster of aged lungs. It implies that reduced Cd4+ T cell population during IAV infection in aged mice linked to disrupted mTOR signaling pathway.

In contrast, Gene Ontology (GO) analysis of CD8+ T cells from young and aged mice revealed an upregulation of the p53 pathway in aged CD8+ T cells, suggesting increased DNA damage may further restrict their proliferative potential. Moreover, We report analysis of lung single cell transcriptome in metformintreated aged mice infected with influenza A virus (IAV) for 9 days. Gene set enrichment analysis of Cd4+ and Cd8+ T cells revealed that metformin treatment positively enriched E2F targets, type I interferon (IFN α) response, and oxidative phosphorylation pathways.

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These findings suggest that metformin improves age associated T cell dysfunction by reducing inhibitory signaling and DNA damage, while enhancing mitochondrial metabolism, E2F and interferon signaling, thereby improving T cell proliferation, function, and viral clearance in aged hosts.

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Inferred from text
RNA sequencing 65%
Provenance · 1 source records, 11 field assertions
SourceKeyLast seenRaw
ScienceDB10.57760/sciencedb.3135412 d agoJSON v1
FieldAssertionExtractorEvidence
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