SCREATE

Cell state · L2

MUSC.early_activation

537 cells in the full atlas (not the displayed sample).

These are the cell-population annotations shown in the SCREATE Cell Browser.

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Marker genes

BCL3, CEBPB, DES, MIR4435-2HG, MT1M, MYC, NNMT, SERPINA3, SOCS3, SOD2

Annotation genes

MYC, NNMT, SOCS3, SOD2

Annotation rationales

Within hours of damage, satellite cells enter a biosynthetic/proliferative ramp: MYC drives ribosome biogenesis and nucleotide flux; NNMT rewires NAD⁺/methyl-donor balance to fuel growth. SOD2 and MT1M buffer mitochondrial ROS/metal stress generated by hypercontraction and macrophage respiratory bursts. Cytokine tuning via SOCS3 (JAK–STAT brake) and BCL3/CEBPB keeps IL-6/IFN signals in a pro-regenerative range. DES (desmin) maintains a myogenic cytoskeleton as cells ready for asymmetric division.

Functional implications

Expand the progenitor pool while resisting oxidative/inflammatory stress. Produce daughter cells that bifurcate into self-renewing and committed myoblast fates, ensuring adequate myonuclei supply for regeneration without exhausting the stem-cell compartment.

Marker and functional descriptions are atlas annotations. Explore gene expression, trait associations and regulatory elements in the interactive browsers; see the browser guide.