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局限性硬皮病患者与健康供体脂肪来源干细胞治疗皮肤纤维化的比较研究。

Comparative Study of Adipose-Derived Stem Cells from Localized Scleroderma Patients and Healthy Donors in Treating Skin Fibrosis.

作者信息

Li Zhujun, Xiao Yiding, Kang Lin, Li Yunzhu, Wang Hayson Chenyu, Li Ziming, Yang Yuemei, Huang Jiuzuo, Yu Nanze, Long Xiao

机构信息

From the Department of Plastic Surgery.

Medical Research Center, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College.

出版信息

Plast Reconstr Surg. 2025 Apr 1;155(4):716e-726e. doi: 10.1097/PRS.0000000000011779. Epub 2024 Sep 30.

Abstract

BACKGROUND

Localized scleroderma (LoS) is an autoimmune disease characterized by fibrosis of the skin and atrophy of the subcutaneous fat tissue. Use of adipose-derived mesenchymal stem cells (ASCs) is a promising treatment approach for LoS. However, ASCs from scleroderma patients (LoS ASCs) have been shown to exhibit altered characteristics compared with ASCs from healthy donors (healthy ASCs). This study aimed to compare the abilities of LoS ASCs and healthy ASCs in treating skin fibrosis.

METHODS

The paracrine ability of ASCs was tested with cytokine array. Bleomycin-challenged mouse models received subcutaneous injection of LoS ASCs and healthy ASCs. Pathologic staining and Western blotting of collagenase type I and α-smooth muscle actin was performed. Fibroblasts derived from LoS lesions (LoS FB) were co-cultured with ASCs, and subjected to RNA sequencing to further explore the similarities and differences in the treatment mechanism.

RESULTS

In vivo comparison revealed that healthy ASCs had a stronger proliferation ability and secreted higher levels of growth factors and cytokines, including vascular endothelial growth factor A, platelet-derived growth factor fibroblasts, and interleukin-10. Pathologic staining of the skin in mouse models treated with ASCs demonstrated that healthy ASCs were more effective in reducing dermal thickness and collagen deposition, and increasing microvessel density and the proportion of M2 macrophages. Co-culture with both healthy ASCs and LoS ASCs reduced the proliferation and migration abilities of LoS FB, and the protein expression of α-smooth muscle actin and collagenase type I. RNA sequencing and validation revealed potential difference in the canonical Wnt pathway.

CONCLUSION

Healthy ASCs exhibited stronger proliferation, paracrine, antifibrosis, proangiogenesis, and immunomodulation abilities in treating skin fibrosis in scleroderma mouse models.

CLINICAL RELEVANCE STATEMENT

Allogenic ASCs obtained from healthy donors are more efficient in treating skin fibrosis, and could serve as a potential alternative for patients who are not suitable candidates for liposuction surgery in the future.

摘要

背景

局限性硬皮病(LoS)是一种自身免疫性疾病,其特征为皮肤纤维化和皮下脂肪组织萎缩。使用脂肪来源的间充质干细胞(ASCs)是一种有前景的LoS治疗方法。然而,与健康供体来源的ASCs(健康ASCs)相比,硬皮病患者来源的ASCs(LoS ASCs)已显示出特征改变。本研究旨在比较LoS ASCs和健康ASCs治疗皮肤纤维化的能力。

方法

用细胞因子阵列检测ASCs的旁分泌能力。博来霉素诱导的小鼠模型皮下注射LoS ASCs和健康ASCs。对Ⅰ型胶原酶和α-平滑肌肌动蛋白进行病理染色和蛋白质印迹分析。将LoS病变来源的成纤维细胞(LoS FB)与ASCs共培养,并进行RNA测序以进一步探索治疗机制的异同。

结果

体内比较显示,健康ASCs具有更强的增殖能力,分泌更高水平的生长因子和细胞因子,包括血管内皮生长因子A、血小板衍生生长因子成纤维细胞和白细胞介素-10。用ASCs治疗的小鼠模型皮肤病理染色表明,健康ASCs在减少真皮厚度和胶原沉积、增加微血管密度和M2巨噬细胞比例方面更有效。与健康ASCs和LoS ASCs共培养均降低了LoS FB的增殖和迁移能力,以及α-平滑肌肌动蛋白和Ⅰ型胶原酶的蛋白表达。RNA测序和验证揭示了经典Wnt信号通路的潜在差异。

结论

在治疗硬皮病小鼠模型的皮肤纤维化方面,健康ASCs表现出更强的增殖、旁分泌、抗纤维化、促血管生成和免疫调节能力。

临床相关性声明

从健康供体获得的同种异体ASCs在治疗皮肤纤维化方面更有效,并且可能成为未来不适合抽脂手术患者的潜在替代方案。

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