← Search

Omics · study · 2026

An aging-sensitive compensatory neuroprotective factor that confers cognitive resilience

Listed in NCBI GEO

Endogenous compensatory changes influence trajectory of brain aging, cognitive decline and Alzheimer’s Disease (AD) risk, however, the identities of underlying mechanisms have remained elusive.

Description

A screen for hippocampal dentate granule cell (DGC) synapse loss-induced factors identified a secreted phospholipase, Pla2g2f, whose expression increases in DGCs during aging. Pla2g2f deletion in DGCs exacerbates aging-associated synapse loss, emergence of inflammatory microglia, reactive astrogliosis, lipid dysregulation and memory impairment.

Boosting Pla2g2f in DGCs during aging prevents these pathophysiological impairments and modifies trajectory of cognitive decline. In human microglia-neuron coculture experiments PLA2G2F mediates intercellular signaling to decrease lipid burden. Boosting Pla2g2f expression in an aging-sensitive AD model reduces amyloid load and preserves memory.

Read the rest (1 more)

Thus, PLA2G2F functions as a compensatory neuroprotective factor that counteracts aging-associated cognitive decline.

Links

Topics

From keywords
Life Sciences
Inferred from text
Disease 75%
Provenance · 1 source records, 8 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE26190614 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[disease].local:disease:diseaseenrichment · NCBI GEOkeyword-concept-rules@1.0.0title+description (75%)
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