Zhang Ying, Bao Yanqiu, Li Zhouna, Jin Zhehu
Department of Dermatology, Shaoxing People's Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), Shaoxing, Zhejiang, China.
Department of Dermatology, Affiliated Hospital of Yanbian University, Yanji, Jilin, China.
J Cosmet Dermatol. 2025 Jun;24(6):e70284. doi: 10.1111/jocd.70284.
Keloid is a common fibroproliferative disorder, often manifesting symptoms such as itching and pain. Given the unique characteristics of keloids, their occurrence is primarily limited to humans, posing difficulties for spontaneous keloid development in animals. Consequently, the creation of animal models has somewhat impeded the comprehensive investigation of keloids.
The aim is to develop a keloid mouse model that mimics the formation process of human keloids, enabling researchers to gain a deeper understanding of their pathophysiological mechanisms and to explore effective therapeutic approaches.
Human keloid fibroblasts were isolated, cultured, and subcutaneously injected with Matrigel into nude mice at four concentrations (1 × 10, 3 × 10, 5 × 10, and 7 × 10 cells). Subcutaneous nodules were transplanted into additional mice to validate stability. Histological and immunohistochemical analyses were performed to assess morphological and molecular features.
Keloid-like nodules formed in a cell density-dependent manner, with the highest concentration group (7 × 10 cells) achieving nodule formation in 39.6 ± 3.2 days, significantly faster than lower concentrations (p < 0.001). The transplantation success rate reached 80%, with nodules exhibiting dense collagen deposition (72.7% ± 3.8%), CD34-positive microvessels (23.1 ± 2.2 vessels/field), and α-SMA expression (11.29% ± 3.7%), closely mirroring human keloid histopathology.
The combination of human keloid fibroblasts and Matrigel provides a simple and rational approach for constructing a nude mouse model, offering a reliable animal model for experimental and clinical research on the pathogenesis and treatment strategies of keloids.
瘢痕疙瘩是一种常见的纤维增生性疾病,常表现出瘙痒和疼痛等症状。鉴于瘢痕疙瘩的独特特征,其发生主要局限于人类,给动物自发形成瘢痕疙瘩带来困难。因此,动物模型的创建在一定程度上阻碍了对瘢痕疙瘩的全面研究。
旨在建立一种模仿人类瘢痕疙瘩形成过程的瘢痕疙瘩小鼠模型,使研究人员能够更深入地了解其病理生理机制,并探索有效的治疗方法。
分离、培养人瘢痕疙瘩成纤维细胞,并将其与基质胶以四种浓度(1×10、3×10、5×10和7×10个细胞)皮下注射到裸鼠体内。将皮下结节移植到其他小鼠中以验证其稳定性。进行组织学和免疫组织化学分析以评估形态和分子特征。
瘢痕疙瘩样结节以细胞密度依赖性方式形成,最高浓度组(7×10个细胞)在39.6±3.2天形成结节,明显快于较低浓度组(p<0.001)。移植成功率达到80%,结节表现出密集的胶原沉积(72.7%±3.8%)、CD34阳性微血管(23.1±2.2个血管/视野)和α-SMA表达(11.29%±3.7%),与人类瘢痕疙瘩组织病理学非常相似。
人瘢痕疙瘩成纤维细胞与基质胶的组合为构建裸鼠模型提供了一种简单合理的方法,为瘢痕疙瘩发病机制和治疗策略的实验和临床研究提供了可靠的动物模型。