Cell-free adipose tissue extracts as a novel treatment for rosacea by downregulating TRPV1

Sci Rep. 2024 Sep 18;14(1):21759. doi: 10.1038/s41598-024-72593-8.

Abstract

Rosacea is a chronic inflammatory skin disease that typically affects the central facial area. Its main clinical symptoms include paroxysmal flushing, telangiectasia, and non-temporary erythema. Cell-free adipose tissue extracts (ATEs) are liquid components extracted from human adipose tissue that contain large amounts of growth factors. Despite the scar-reducing, anti-aging, and wound-healing effects of ATEs, the efficacy of ATEs in rosacea remains unknown. Therefore, the anti-rosacea effects of ATEs were investigated in human cathelicidin peptide (LL-37) induced rosacea mice and capsaicin (CAP)-stimulated HaCaT keratinocytes. In vitro, ATEs significantly reduced TRPV1 expression, intracellular calcium ions influx and the release of inflammatory factors (such as KLK5, IL-6, IL-8 and TNF-α) after intervening in CAP-stimulated cells. The in vivo results revealed that ATEs alleviated rosacea symptoms, such as erythema score, erythema area, transepidermal water loss, abnormal epidermal thickness, mast cell infiltration and telangiectasia upon downregulating TRPV1 and CD31 expression. Moreover, the up-regulated TRPV1 protein expression was also recovered by ATEs administration in vivo and in vitro. Meanwhile, ATEs demonstrated good biocompatibility. In summary, ATEs could be a potential therapeutic agent for rosacea by regulating inflammation and alleviating telangiectasia.

Keywords: Cell-free adipose tissue extracts; Inflammation; Rosacea; TRPV1.

MeSH terms

  • Adipose Tissue* / drug effects
  • Adipose Tissue* / metabolism
  • Animals
  • Antimicrobial Cationic Peptides / metabolism
  • Antimicrobial Cationic Peptides / pharmacology
  • Capsaicin / pharmacology
  • Cathelicidins
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • HaCaT Cells
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Male
  • Mice
  • Rosacea* / drug therapy
  • Rosacea* / metabolism
  • Rosacea* / pathology
  • TRPV Cation Channels* / metabolism

Substances

  • TRPV Cation Channels
  • Capsaicin
  • TRPV1 protein, mouse
  • Cathelicidins
  • TRPV1 protein, human
  • Antimicrobial Cationic Peptides