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一种可注射的光交联丝素水凝胶系统通过时空免疫调节增强了骨科手术中糖尿病伤口的愈合。

An injectable photo-cross-linking silk hydrogel system augments diabetic wound healing in orthopaedic surgery through spatiotemporal immunomodulation.

机构信息

Department of Orthopaedics, First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.

Department of Orthopaedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, Shanghai, 200233, China.

出版信息

J Nanobiotechnology. 2022 May 14;20(1):232. doi: 10.1186/s12951-022-01414-9.

Abstract

BACKGROUND

The complicated hyperglycaemic and chronic inflammation of diabetic wounds in orthopaedic surgery leads to dysregulated immune cell function and potential infection risk. Immune interventions in diabetic wounds face a possible contradiction between simultaneous establishment of the pro-inflammatory microenvironment in response to potential bacterial invasion and the anti-inflammatory microenvironment required for tissue repair. To study this contradiction and accelerate diabetic-wound healing, we developed a photocurable methacryloxylated silk fibroin hydrogel (Sil-MA) system, co-encapsulated with metformin-loaded mesoporous silica microspheres (MET@MSNs) and silver nanoparticles (Ag NPs).

RESULTS

The hydrogel system (M@M-Ag-Sil-MA) enhanced diabetic-wound healing via spatiotemporal immunomodulation. Sil-MA imparts a hydrogel system with rapid in situ Ultra-Violet-photocurable capability and allows preliminary controlled release of Ag NPs, which can inhibit bacterial aggregation and create a stable, sterile microenvironment. The results confirmed the involvement of Met in the immunomodulatory effects following spatiotemporal dual-controlled release via the mesoporous silica and Sil-MA. Hysteresis-released from Met shifts the M1 phenotype of macrophages in regions of diabetic trauma to an anti-inflammatory M2 phenotype. Simultaneously, the M@M-Ag-Sil-MA system inhibited the formation of neutrophil extracellular traps (NETs) and decreased the release of neutrophil elastase, myeloperoxidase, and NETs-induced pro-inflammatory factors. As a result of modulating the immune microenvironmental, the M@M-Ag-Sil-MA system promoted fibroblast migration and endothelial cell angiogenesis in vivo, with verification of enhanced diabetic-wound healing accompanied with the spatiotemporal immunoregulation of macrophages and NETs in a diabetic mouse model.

CONCLUSIONS

Our findings demonstrated that the M@M-Ag-Sil-MA hydrogel system resolved the immune contradiction in diabetic wounds through spatiotemporal immunomodulation of macrophages and NETs, suggesting its potential as a promising engineered nano-dressing for the treatment of diabetic wounds in orthopaedic surgery.

摘要

背景

骨科手术中糖尿病伤口的复杂高血糖和慢性炎症导致免疫细胞功能失调和潜在的感染风险。糖尿病伤口的免疫干预面临着一个潜在的矛盾,即在潜在细菌入侵时同时建立促炎微环境和组织修复所需的抗炎微环境。为了研究这种矛盾并加速糖尿病伤口愈合,我们开发了一种可光固化的甲氧基丙烯酰化丝素蛋白水凝胶(Sil-MA)系统,该系统共包载了载有二甲双胍的介孔硅微球(MET@MSNs)和银纳米粒子(Ag NPs)。

结果

水凝胶系统(M@M-Ag-Sil-MA)通过时空免疫调节促进糖尿病伤口愈合。Sil-MA 赋予水凝胶系统快速的原位紫外线光固化能力,并允许初步控制 Ag NPs 的释放,Ag NPs 可以抑制细菌聚集并创造稳定、无菌的微环境。结果证实,通过介孔硅和 Sil-MA 的时空双控释放,Met 参与了免疫调节作用。从 Met 中释放的滞后使糖尿病创伤区域的巨噬细胞从 M1 表型转变为抗炎的 M2 表型。同时,M@M-Ag-Sil-MA 系统抑制中性粒细胞胞外诱捕网(NETs)的形成,并减少中性粒细胞弹性蛋白酶、髓过氧化物酶和 NETs 诱导的促炎因子的释放。通过调节免疫微环境,M@M-Ag-Sil-MA 系统促进了体内成纤维细胞迁移和内皮细胞血管生成,在糖尿病小鼠模型中证实了糖尿病伤口愈合的增强,同时伴有巨噬细胞和 NETs 的时空免疫调节。

结论

我们的研究结果表明,M@M-Ag-Sil-MA 水凝胶系统通过时空调节巨噬细胞和 NETs 的免疫反应解决了糖尿病伤口中的免疫矛盾,表明其作为一种有前途的工程纳米敷料用于治疗骨科手术中的糖尿病伤口的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8322/9107711/49bddb120a32/12951_2022_1414_Fig1_HTML.jpg

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