Client research ·

Single-cell and epigenomic insights into adipose hyperplasia in port-wine stains

Cell populations, chromatin accessibility and expression data inform investigation of SPSB1 and HDAC1.

Research question

This client research investigates subcutaneous adipose hyperplasia in facial port-wine stains, connecting cellular composition with regulatory mechanisms.

Omics approach

Single-cell analysis identifies populations including adipose stem and progenitor cells. ATAC and RNA data provide complementary evidence on chromatin accessibility and expression.

Mechanistic follow-up

The study examines how SPSB1 affects HDAC1 degradation and stability, with experimental follow-up including ChIP-qPCR. Multiple data types address a shared mechanistic question.

Paper and source

SPSB1 Promotes Subcutaneous Adipose Hyperplasia in Facial Port-Wine Stains by Controlling HDAC1 Degradation and Stability Through Two Distinct Proteolytic Pathways

Advanced Science

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