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用于促进脂肪生成的脂肪来源干细胞特异性亲和肽修饰的去细胞脂肪支架

Adipose-Derived Stem Cell Specific Affinity Peptide-Modified Adipose Decellularized Scaffolds for Promoting Adipogenesis.

作者信息

Qin Jiahang, Wang Ruoxi, Liang Wei, Man Zhentao, Li Wei, An Yang, Chen Haifeng

机构信息

Department of Biomedical Engineering, College of Future Technology, Peking University, Beijing 100871, China.

Department of Plastic Surgery, Peking University Third Hospital, Beijing 100191, China.

出版信息

ACS Biomater Sci Eng. 2025 Mar 10;11(3):1705-1720. doi: 10.1021/acsbiomaterials.4c02161. Epub 2025 Feb 19.

Abstract

Adipose-derived stem cells (ADSCs) are known to promote angiogenesis and adipogenesis. However, their limited ability to efficiently target and integrate into specific tissues poses a major challenge for ADSC-based therapies. In this study, we identified a seven-amino acid peptide sequence (P7) with high specificity for ADSCs using phage display technology. P7 was then covalently conjugated to decellularized adipose-derived matrix (DAM), creating an "ADSC homing device" designed to recruit ADSCs both in vitro and in vivo. The P7-conjugated DAM significantly enhanced ADSC adhesion and proliferation in vitro. After being implanted into rat subcutaneous tissue, immunofluorescence staining after 14 days revealed that P7-conjugated DAM recruited a greater number of ADSCs, promoting angiogenesis and adipogenesis in the surrounding tissue. Moreover, CD206 immunostaining at 14 days indicated that P7-conjugated DAM facilitated the polarization of macrophages to the M2 phenotype at the implantation site. These findings demonstrate that the P7 peptide has a high affinity for ADSCs, and its conjugation with DAM significantly improves ADSC recruitment in vivo. This approach holds great potential for a wide range of applications in material surface modification.

摘要

脂肪来源干细胞(ADSCs)已知可促进血管生成和脂肪生成。然而,它们有效靶向并整合到特定组织中的能力有限,这对基于ADSC的治疗构成了重大挑战。在本研究中,我们使用噬菌体展示技术鉴定了一种对ADSCs具有高特异性的七氨基酸肽序列(P7)。然后将P7共价偶联到脱细胞脂肪来源基质(DAM)上,创建了一种“ADSC归巢装置”,旨在在体外和体内募集ADSCs。P7偶联的DAM在体外显著增强了ADSC的粘附和增殖。植入大鼠皮下组织14天后,免疫荧光染色显示P7偶联的DAM募集了更多的ADSCs,促进了周围组织的血管生成和脂肪生成。此外,14天时的CD206免疫染色表明,P7偶联的DAM促进了植入部位巨噬细胞向M2表型的极化。这些发现表明,P7肽对ADSCs具有高亲和力,其与DAM的偶联显著改善了体内ADSC的募集。这种方法在材料表面改性的广泛应用中具有巨大潜力。

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