• Single-cell transcriptomics of facial adipose tissue reveals a distinct cellular landscape in FIL, with fibro-adipogenic precursor cells (FAPs) showing significant overexpression of FKBP5.
• FKBP5 expression is regulated by the PI3K-AKT signaling pathway, linking PIK3CA mutations to downstream adipogenic mechanisms.
• Functional studies demonstrate that FKBP5 promotes adipogenic differentiation of FAPs, and its knockdown or inhibition impedes this process, both in vitro and in vivo.
• FKBP5 emerges as a promising therapeutic target for non-surgical management of facial infiltrating lipomatosis, potentially reducing recurrence and surgical complications.
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