Innovative applications of acellular adipose matrix derived film in skin soft tissue expansion

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2025-08-01 Epub Date: 2025-03-24 DOI:10.1016/j.bioadv.2025.214291
Baoyan Liang , Ruoxue Bai , Jiayang Wang , Shuyang Shi , Yajie Guo , Qi Wang , Han Peng , Jiezhang Tang , Shuai Liu , Jun Zhu , Chenggang Yi , Mengmeng Hou , Huichen Li
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Abstract

Background

Skin dilation generates “extra” skin tissue through mechanical traction, but its effectiveness is limited by the proliferation capacity of keratinocytes, fibroblasts and the level of angiogenesis. Cutaneous application of drug and subcutaneous injection are common interventions to promote skin dilation, but they have defects such as uneven drug distribution, high risk of infection and single targeting. Although Acellular adipose matrix (AAM) has the potential to promote cell proliferation and angiogenesis, its hydrogel/powder dosage forms still need frequent injection, which limits clinical application.

Results

In this study, Acellular adipose matrix derived film (AAF) was successfully developed, and a flexible film was formed by acellular - lyophilized - enzymolysis - self-assembly process. In vitro experiments confirmed that AAF significantly promoted the activity of Human Immortalized Epidermal Cells (HaCaTs), Normal Skin Fibroblasts (NFbs) and Human Umbilical Endothelial Cells (HUVECs); It was also found that AAF can induce adipose mesenchymal stem cells (ASCs) to differentiate into adipocytes and promote subcutaneous fat regeneration. In vivo, the rat model showed that AAF wrapping expander could effectively improve the skin expansion efficiency, promote the skin thickness increase in the expanded area, and the density of new blood vessels was significantly increased compared with the comparative group, and there was no complication such as infection or skin collapse. It was found for the first time that AAF successfully formed new adipose tissue in the subcutaneous area.

Conclusion

AAF innovatively integrates the bionic structure of extracellular matrix and slow-release function, and solves the uneven drug distribution and associated infection risk of traditional intervention methods by regulating the synergistic regeneration of epidermodermis and vascular units. Its mechanical adaptability (dry toughness/wet plasticity) and the ability of inducing adipose regeneration provide a new strategy of both structural strengthening and metabolic support for skin dilation, also laying a mechanism and empirical foundation for clinical transformation of tissue engineering materials.
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脱细胞脂肪基质衍生膜在皮肤软组织扩张中的创新应用
背景:皮肤扩张通过机械牵引产生“额外”的皮肤组织,但其有效性受到角质形成细胞、成纤维细胞的增殖能力和血管生成水平的限制。皮肤用药和皮下注射是促进皮肤扩张的常用干预措施,但存在药物分布不均匀、感染风险高、靶向单一等缺陷。虽然脱细胞脂肪基质(AAM)具有促进细胞增殖和血管生成的潜力,但其水凝胶/粉末剂型仍需要频繁注射,限制了临床应用。结果本研究成功制备了脱细胞脂肪基质衍生膜(AAF),并通过脱细胞-冻干-酶解-自组装工艺制备了柔性膜。体外实验证实,AAF能显著促进人永生化表皮细胞(HaCaTs)、正常皮肤成纤维细胞(NFbs)和人脐内皮细胞(HUVECs)的活性;还发现AAF能诱导脂肪间充质干细胞(ASCs)向脂肪细胞分化,促进皮下脂肪再生。体内大鼠模型显示,AAF包覆扩张器能有效提高皮肤扩张效率,促进扩张区皮肤厚度增加,新生血管密度较对照组明显增加,无感染、皮肤塌陷等并发症。首次发现AAF在皮下成功形成新的脂肪组织。结论aaf创新性地整合了细胞外基质的仿生结构和缓释功能,通过调节表皮和血管单位的协同再生,解决了传统干预方法的药物分布不均匀和相关感染风险。其机械适应性(干韧性/湿塑性)和诱导脂肪再生能力为皮肤扩张提供了结构强化和代谢支持的新策略,也为组织工程材料的临床转化奠定了机制和经验基础。
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来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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