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Omics · study · 2026

Loss of G9a in myofiber accelerates muscle regeneration

Listed in NCBI GEO

Age-related muscle regenerative capacity decline is related to the disruption of the Injured skeletal muscle regenerates through a network orchestrated by multiple muscle-harbored cell types, however, yet the contribution of the interplay between macrophages and myofibers upon injuryto this process is largely unknown.

Description

Deletion of G9a in myofiber mitigates muscle aging and accelerates muscle regeneration. Mechanistically, by deleting Osteocrin (musclin-encoding) in myofiber-specific G9a knockout background, we found G9a suppresses myofiber-derived musclin to inhibit myogenesis and macrophage phenotype transition during muscle regeneration.Musclin recombination protein accelerated muscle regeneration.

Collectively, we highlight an epigenetic mechanism that links muscle aging to muscle regeneration, G9a serves an epigenetic hallmark of muscle aging and a the crosstalk between myofibers and macrophages , both regulated by G9a, steers a pro-recovery microenvironment after muscle injury, which offers therapeutic potentials for muscle regenerative capacity decline in the aged.

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Life Sciences
Provenance · 1 source records, 7 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE29952313 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
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