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具有高皮肤再生潜力的抗菌肽-金纳米尺度治疗制剂。

Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential.

机构信息

CNC-Center for Neurosciences and Cell Biology, University of Coimbra, 3000 Coimbra, Portugal.

CNC-Center for Neurosciences and Cell Biology, University of Coimbra, 3000 Coimbra, Portugal; Faculty of Medicine, University of Coimbra, 3000-548 Coimbra, Portugal.

出版信息

J Control Release. 2017 Sep 28;262:58-71. doi: 10.1016/j.jconrel.2017.07.007. Epub 2017 Jul 8.

DOI:10.1016/j.jconrel.2017.07.007
PMID:28694030
Abstract

Chronic skin wounds affect ≈3% of persons aged >60years (Davies et al., 2007) [1]. These wounds are typically difficult to heal by conventional therapies and in many cases they get infected making even harder the regeneration process. The antimicrobial peptide (AMP) LL37 combines antimicrobial with pro-regenerative properties and thus represents a promising topical therapy to address both problems. Here, we investigated the wound healing potential of soluble and immobilized LL37 (LL37-conjugated gold nanoparticles, LL37-Au NPs), both in vitro (migration of keratinocytes) and in vivo (skin wound healing). Our results show that LL37-Au NPs, but not LL37 peptide, have the capacity to prolong the phosphorylation of EGFR and ERK1/2 and enhance the migratory properties of keratinocytes in a large in vitro wound model. We further report that both LL37 and LL37-Au NPs promote keratinocyte migration by the transactivation of EGFR, a process that seems to be initiated at the P2X7 receptor, as confirmed by chemical and genetic inhibition studies. Finally, we show in vivo that LL37-Au NPs have higher wound healing activity than LL37 peptide in a splinted mouse full thickness excisional model. Animal wounds treated by LL37-Au NPs have higher expression of collagen, IL6 and VEGF than the ones treated with LL37 peptide or NPs without LL37. Altogether, the conjugation of AMPs to NPs offers a promising platform to enhance their pro-regenerative properties.

摘要

慢性皮肤伤口影响了约 3%的 >60 岁人群(Davies 等人,2007 年)[1]。这些伤口通常很难通过传统疗法愈合,而且在许多情况下它们会感染,这使得再生过程更加困难。抗菌肽(AMP)LL37 具有抗菌和促进再生的特性,因此代表了一种有前途的局部治疗方法,可以解决这两个问题。在这里,我们研究了可溶性和固定化 LL37(LL37 缀合金纳米粒子,LL37-Au NPs)的伤口愈合潜力,包括在体外(角质形成细胞迁移)和体内(皮肤伤口愈合)。我们的结果表明,LL37-Au NPs,但不是 LL37 肽,具有延长 EGFR 和 ERK1/2 磷酸化以及增强体外大伤口模型中角质形成细胞迁移能力的能力。我们进一步报告说,LL37 和 LL37-Au NPs 都通过 EGFR 的跨激活促进角质形成细胞迁移,这一过程似乎是由 P2X7 受体启动的,这一点得到了化学和遗传抑制研究的证实。最后,我们在体内显示,在夹板小鼠全厚度切除模型中,LL37-Au NPs 的伤口愈合活性高于 LL37 肽。与用 LL37 肽或不含 LL37 的 NPs 治疗的动物伤口相比,用 LL37-Au NPs 治疗的动物伤口中胶原蛋白、IL6 和 VEGF 的表达更高。总之,将 AMP 缀合到 NPs 上为增强其促再生特性提供了一个很有前途的平台。

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