AI Article Synopsis
- Objective: The study aimed to create animal models of keloids using tissue engineering techniques to evaluate their potential for clinical and laboratory research.
- Methods: Fibroblasts from keloids were isolated and cultured, then transplanted into a biodegradable polymer (PLGA) and into athymic mice for analysis after 4 and 8 weeks.
- Results: All mice survived, and after 8 weeks, keloid-like collagen patterns were observed, indicating that the fibroblasts retained their ability to synthesize collagen, showing promise for further research.
Article Abstract
Objective: To build animal models of keloid by method of tissue engineering and to discuss the feasibility of using it in clinical and lab researches.
Methods: Fibroblasts(FB) were isolated from keloids and cultured. The seventh and eighth generation of the cultured FBs were inoculated into the copolymers of polylactic acid and polyglycolic PLGA. After being cultured in rotatory cell culture system (RCCS) for 1 week, the FB was transplanted into athymic mice. The specimens were obtained 4 weeks and 8 weeks and examined histologically.
Results: All mice survived. The collagen patterns of all keloids were pressed in every specimen obtained 8 weeks. Fibrocytes and FB were observed in specimens by electronic microscope. There were abundant rough endoplasmic reticulum (RER) in FB, which indicated that FB's capability of synthesizing and secreting collagen was preserved and the cellular characteristic was remained.
Conclusion: There is a good affinity between PLGA and FB. The composition of PLGA and FB can form keloids in athymic mice, so that it deserves further researching and developing.
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