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Omics · study · 2026

Transcriptomic evaluation of Mef2c manipulation in the mouse brain and HT22 cells

Listed in NCBI GEO

The objective of this study is to elucidate the transcriptomic mechanisms underlying Mef2c-regulated cognitive aging and to determine whether intact Mef2c signaling is required for the antiaging transcriptomic effects of Dasatinib plus Quercetin (D+Q) and Spermidine (SPD).

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To evaluate its physiological impact, we manipulated Mef2c expression in the mouse brain using lentiviral vectors and performed transcriptomic profiling.

In 19-month-old aged mice, overexpressing Mef2c (Mef2c OE) upregulated genes enriched in learning, memory, and neuron differentiation, while effectively repressing stress-activated signaling and chemokine production. Conversely, knocking down Mef2c (siMef2c) in 11-month-old middle-aged mice induced a transcriptomic shift towards heightened oxidative stress and neuronal death, coupled with the suppression of cognition and synaptic transmission pathways.

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Furthermore, to evaluate whether silencing Mef2c abolishes the observed antiaging effects of D+Q and SPD in cultured neurons, we pre-treated HT22 cells with siMef2c followed by D+Q or SPD administration. Transcriptomic profiling revealed that under conditions of Mef2c depletion, neither D+Q nor SPD could elicit the antiaging transcriptomic signatures previously observed in the brain. This confirms that an intact Mef2c signaling is indispensable for their full neuroprotective actions.

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Life Sciences
Provenance · 1 source records, 8 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE33601813 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[field].anzsrc:group:3102enrichment · NCBI GEOtaxonomy-embedding@1.1.0title+keywords+description (69%)
concepts[field].local:field:life-sciencesmapping · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[method].geo_series_type:expression-profiling-by-high-throughput-sequencingsource · NCBI GEOconnector:ncbi_geo@1.0.0/gdstype
concepts[organism].NCBITaxon:10090source · NCBI GEOconnector:ncbi_geo@1.0.0/taxon
descriptionsource · NCBI GEOconnector:ncbi_geo@1.0.0/summary
publication_datesource · NCBI GEOconnector:ncbi_geo@1.0.0
titlesource · NCBI GEOconnector:ncbi_geo@1.0.0/title