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Isolation, Culture, and Characterization of Primary Dermal Fibroblasts from Human Keloid Tissue
Published on: July 28, 2023
Keloid Patient Plasma-Derived Exosomal hsa_circ_0020792 Promotes Normal Skin Fibroblasts Proliferation, Migration,
Huan Hu1, Guangyu Mao1, Jianghong Zheng1
1Department of Plastic Surgery, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, People's Republic of China.
Exosomes from keloid patients contain elevated hsa_circ_0020792, a molecule that drives keloid fibroblast proliferation and migration. This finding offers new insights into keloid pathogenesis and potential therapeutic targets.
Area of Science:
- Biochemistry
- Molecular Biology
- Dermatology
Background:
- Keloids are fibroproliferative disorders impacting patient quality of life.
- Circular RNAs (circRNAs) in exosomes are implicated in diseases, but their role in keloids is unclear.
- Hsa_circ_0020792 is upregulated in keloid tissues, yet its function in plasma-derived exosomes is unknown.
Purpose of the Study:
- To investigate the role of hsa_circ_0020792 within exosomes derived from keloid patient plasma.
- To determine the impact of exosomal hsa_circ_0020792 on normal skin fibroblasts (NFs).
- To elucidate the molecular mechanisms by which exosomal hsa_circ_0020792 influences keloid formation.
Main Methods:
- Exosomes were isolated from plasma of keloid patients and healthy controls.
- Quantitative reverse transcription PCR (RT-qPCR) was used to measure hsa_circ_0020792 and miR-193a-5p levels.
- Effects on fibroblast viability, migration, extracellular matrix synthesis, apoptosis, and fibrogenesis were assessed.
Main Results:
- Keloid patient exosomes showed significantly higher hsa_circ_0020792 levels compared to controls.
- These exosomes promoted NF proliferation, migration, and extracellular matrix synthesis, while reducing apoptosis.
- Downregulation of hsa_circ_0020792 reversed these effects, implicating it in fibrogenesis via TGF-β signaling and miR-193a-5p modulation.
Conclusions:
- Plasma-derived exosomal hsa_circ_0020792 promotes keloid fibroblast proliferation, migration, and fibrogenesis.
- This process involves the modulation of miR-193a-5p and activation of the TGF-β1/Smad2/3 signaling pathway.
- Exosomal hsa_circ_0020792 represents a potential biomarker and therapeutic target for keloids.
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