Exosomes Derived from Hypertrophic Scar Fibroblasts Suppress Melanogenesis in Normal Human Epidermal Melanocytes

• Published in: International journal of molecular sciences 2024-07, Vol.25 (13), p.7236
• Main Authors: Cui, Hui Song, Joo, So Young, Cho, Yoon Soo, Lee, You Ra, Ro, Yu Mi, Kwak, In Suk, Hur, Gi Yeun, Seo, Cheong Hoon
• Format: Article
• Language: English
• Subjects: Apoptosis; Cell growth; Cell Proliferation; Cells, Cultured; Cellular signal transduction; Cicatrix, Hypertrophic - metabolism; Cicatrix, Hypertrophic - pathology; Communication; DNA binding proteins; Enzymes; Epidermis - metabolism; Epidermis - pathology; Exosomes - metabolism; Fibroblasts; Fibroblasts - metabolism; Free radicals (Chemistry); Growth factors; Humans; Kinases; Medical research; Medicine, Experimental; Melanins - biosynthesis; Melanins - metabolism; Melanocytes - metabolism; Melanogenesis; Physiological aspects; Physiology; Proteins; Signal Transduction; Skin; Ultraviolet radiation
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25137236

Post-burn hypertrophic scars often exhibit abnormal pigmentation. Exosomes play important roles in maintaining normal physiological homeostasis and in the pathological development of diseases. This study investigated the effects of the exosomes derived from hypertrophic scar fibroblasts (HTSFs) on melanocytes, which are pigment-producing cells. Normal fibroblasts (NFs) and HTSFs were isolated and cultured from normal skin and hypertrophic scar (HTS) tissue. Both the NF- and HTSF-exosomes were isolated from a cell culture medium and purified using a column-based technique. The normal human epidermal melanocytes were treated with both exosomes at a concentration of 100 μg/mL at different times. The cell proliferation, melanin content in the medium, apoptotic factors, transcription factors, melanin synthesis enzymes, signaling, signal transduction pathways, and activators of transcription factors (STAT) 1, 3, 5, and 6 were investigated. Compared with the Dulbecco's phosphate-buffered saline (DPBS)-treated controls and NF-exosomes, the HTSF-exosomes decreased the melanocyte proliferation and melanin secretion. The molecular patterns of apoptosis, proliferation, melanin synthesis, Smad and non-Smad signaling, and STATs were altered by the treatment with the HTSF-exosomes. No significant differences were observed between the DPBS-treated control and NF-exosome-treated cells. HTSF-derived exosomes may play a role in the pathological epidermal hypopigmentation observed in patients with HTS.