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纳米复合水凝胶中脂质体 SDF-1 Alpha 的递呈促进巨噬细胞表型改变和皮肤组织再生。

Liposomal SDF-1 Alpha Delivery in Nanocomposite Hydrogels Promotes Macrophage Phenotype Changes and Skin Tissue Regeneration.

机构信息

Fischell Department of Bioengineering, University of Maryland, College Park, 3121 A. James Clark Hall, 8278 Paint Branch Drive, College Park, Maryland 20742, United States.

NIH/NBIB Center for Engineering Complex Tissues, University of Maryland, College Park, 3121 A. James Clark Hall, 8278 Paint Branch Drive, College Park, Maryland 20742, United States.

出版信息

ACS Biomater Sci Eng. 2021 Nov 8;7(11):5230-5241. doi: 10.1021/acsbiomaterials.1c01140. Epub 2021 Oct 26.

DOI:10.1021/acsbiomaterials.1c01140
PMID:34699182
Abstract

Skin regeneration in chronic wounds is often delayed due to persistent inflammation induced by underlying conditions such as diabetes. This effect is mediated, in part, by macrophages present in the wound, which can be stimulated to adopt either pro- or anti-inflammatory phenotypes depending on the status of the local microenvironment. In this work, the prohealing chemokine stromal cell-derived factor-1 alpha (SDF-1α) is controllably released from a hydrogel-based biomaterial to promote skin tissue regeneration and wound closure. This innovative nanocomposite hydrogel system releases liposomal stromal cell-derived factor-1 alpha (lipoSDF) as a new treatment approach for dorsal full-thickness skin wounds in wild-type and diabetic mice. Using this strategy, the recruitment and polarization of macrophages primarily of the anti-inflammatory phenotype were observed, along with a decreased amount of open wound surface area in diabetic mice after 28 days. This was accompanied by histological observations of increased epidermal stratification and dermal angiogenesis. These findings represent an important step of investigation distinctive in its field for developing immunomodulatory biomaterials that are able to influence macrophage phenotype and promote healing as hydrogel-based wound dressings.

摘要

慢性伤口的皮肤再生通常会因糖尿病等潜在疾病引起的持续炎症而延迟。这种影响部分是由伤口中存在的巨噬细胞介导的,根据局部微环境的状态,巨噬细胞可以被刺激采用促炎或抗炎表型。在这项工作中,促愈趋化因子基质细胞衍生因子-1 ɑ(SDF-1ɑ)可从基于水凝胶的生物材料中受控释放,以促进皮肤组织再生和伤口闭合。这种创新的纳米复合水凝胶系统将脂质体基质细胞衍生因子-1 ɑ(lipoSDF)作为一种新的治疗方法,用于野生型和糖尿病小鼠的背部全层皮肤伤口。使用这种策略,观察到巨噬细胞的募集和极化主要是抗炎表型,并且在 28 天后糖尿病小鼠的开放性伤口表面积减少。这伴随着表皮分层和真皮血管生成增加的组织学观察。这些发现代表了在开发能够影响巨噬细胞表型并促进愈合的免疫调节生物材料方面的一个重要研究步骤,这些生物材料可作为水凝胶为基础的伤口敷料。

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