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径向排列纳米纤维支架洗脱的 25-羟维生素 D 可增强人源化免疫小鼠防御素的产生,同时降低炎症反应。

Eluted 25-hydroxyvitamin D from radially aligned nanofiber scaffolds enhances cathelicidin production while reducing inflammatory response in human immune system-engrafted mice.

机构信息

Department of Surgery-Transplant and Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.

Chongqing Academy of Animal Sciences & Key Laboratory of Pig Industry Sciences, Ministry of Agriculture, Chongqing, China.

出版信息

Acta Biomater. 2019 Oct 1;97:187-199. doi: 10.1016/j.actbio.2019.08.005. Epub 2019 Aug 3.

Abstract

Vitamin D modulates immune response, induces endogenous antimicrobial peptide production, and enhances innate immunity to defend against infections. These findings suggest that incorporating vitamin D into medical devices or scaffolds could positively modulate host immune response and prevent infections. In the current study, we evaluated host responses and endogenous antimicrobial peptide production using 25-hydroxyvitamin D (25(OH)D)-eluting radially aligned PCL nanofiber scaffolds in human immune system-engrafted mice. We transformed traditional 2D electrospun nanofiber membranes into radially aligned PCL nanofiber scaffolds using the concept of solid of revolution and an innovative gas-foaming technique. Such scaffolds can promote rapid cellular infiltration and neovascularization. The infiltrating immune cells within subcutaneously implanted 25(OH)D-containing scaffolds mainly consisted of human macrophages in the M1 phase (CCR7), mice macrophages in the M2 phase (CD206), and human cytotoxic T cells (CD8) other than few human T-helper cells (CD4). The 25(OH)D-eluting nanofiber scaffolds significantly inhibited the production of pro-inflammatory cytokines (TNF-α, IL-6), while accelerating the production of anti-inflammatory cytokines (IL-4, IL-10) within the scaffolds. Additionally, we observed increased expression of human cathelicidin LL-37 within the 25(OH)D-eluting scaffolds, while no LL-37 expression was observed in the control. Together, these findings support further work in the design of vitamin D-eluting medical devices or scaffolds for modulating immune response and promoting antimicrobial peptide production. This could potentially reduce the inflammatory response, prevent infections, and eventually improve success rates of implants. STATEMENT OF SIGNIFICANCE: Transplant failure of medical devices, grafts, scaffolds, and tissue-engineered constructs due to inflammation and infection causes not only economic losses but also sufferings of second operation to the patient. Positive modulation of the host response to implants, scaffolds, and tissue-engineered constructs is likely to reduce the failure rate. Vitamin D plays an important role in modulating the immune response. It is able to not only reduce inflammation and induce endogenous antimicrobial peptide production but also prevent multidrug resistance and other side effects of traditional antibiotics. In this study, host responses to 25-hydroxyvitamin D (25(OH)D)-eluting radially aligned PCL nanofiber scaffolds were evaluated in human immune system-engrafted mice. The 25(OH)D-eluting medical devices or scaffolds were able to modulate positive immune response and promote antimicrobial peptide production. This work presented an innate immunity-enhancing approach for reducing the inflammatory response and preventing infections, likely resulting in improvement of success rates of implants.

摘要

维生素 D 可调节免疫反应,诱导内源性抗菌肽的产生,并增强先天免疫以抵御感染。这些发现表明,将维生素 D 纳入医疗器械或支架中可以积极调节宿主的免疫反应并预防感染。在本研究中,我们使用人免疫系统移植小鼠中的 25-羟维生素 D(25(OH)D)洗脱的放射状排列的 PCL 纳米纤维支架来评估宿主反应和内源性抗菌肽的产生。我们使用旋转体的概念和创新的气体发泡技术将传统的 2D 静电纺纳米纤维膜转化为放射状排列的 PCL 纳米纤维支架。这种支架可以促进细胞的快速浸润和新血管生成。皮下植入含有 25(OH)D 的支架内浸润的免疫细胞主要由 M1 期(CCR7)的人巨噬细胞、M2 期(CD206)的小鼠巨噬细胞和人细胞毒性 T 细胞(CD8)组成,而不是少数人辅助性 T 细胞(CD4)。25(OH)D 洗脱纳米纤维支架显著抑制了促炎细胞因子(TNF-α、IL-6)的产生,同时加速了支架内抗炎细胞因子(IL-4、IL-10)的产生。此外,我们观察到在 25(OH)D 洗脱支架中表达的人 cathelicidin LL-37 增加,而在对照中未观察到 LL-37 的表达。总之,这些发现支持进一步设计洗脱维生素 D 的医疗器械或支架来调节免疫反应和促进抗菌肽的产生。这可能会降低炎症反应,预防感染,并最终提高植入物的成功率。

意义声明

由于炎症和感染导致医疗器械、移植物、支架和组织工程构建体的移植失败不仅会造成经济损失,还会给患者带来第二次手术的痛苦。对植入物、支架和组织工程构建体的宿主反应进行积极调节可能会降低失败率。维生素 D 在调节免疫反应中起着重要作用。它不仅能减少炎症和诱导内源性抗菌肽的产生,还能防止传统抗生素的多重耐药性和其他副作用。在这项研究中,我们在人免疫系统移植小鼠中评估了 25-羟维生素 D(25(OH)D)洗脱的放射状排列的 PCL 纳米纤维支架对宿主的反应。洗脱维生素 D 的医疗器械或支架能够调节免疫反应,促进抗菌肽的产生。这项工作提出了一种增强固有免疫的方法,以减少炎症反应和预防感染,可能会提高植入物的成功率。

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本文引用的文献

1
Fabrication of injectable and superelastic nanofiber rectangle matrices ("peanuts") and their potential applications in hemostasis.
Biomaterials. 2018 Oct;179:46-59. doi: 10.1016/j.biomaterials.2018.06.031. Epub 2018 Jun 22.
2
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Nanomedicine (Lond). 2018 Jun;13(12):1417-1432. doi: 10.2217/nnm-2018-0011. Epub 2018 Jul 4.
3
Copper-containing mesoporous bioactive glass promotes angiogenesis in an in vivo zebrafish model.
Acta Biomater. 2018 Mar 1;68:272-285. doi: 10.1016/j.actbio.2017.12.032. Epub 2017 Dec 27.
5
Humanized mice in studying efficacy and mechanisms of PD-1-targeted cancer immunotherapy.
FASEB J. 2018 Mar;32(3):1537-1549. doi: 10.1096/fj.201700740R. Epub 2018 Jan 3.
6
Nanofiber-based sutures induce endogenous antimicrobial peptide.
Nanomedicine (Lond). 2017 Nov;12(21):2597-2609. doi: 10.2217/nnm-2017-0161. Epub 2017 Sep 29.
7
Modulation of Inflammatory Response to Implanted Biomaterials Using Natural Compounds.
Curr Pharm Des. 2017;23(41):6347-6357. doi: 10.2174/1381612823666170510124348.
8
Humanized mouse model for assessing the human immune response to xenogeneic and allogeneic decellularized biomaterials.
Biomaterials. 2017 Jun;129:98-110. doi: 10.1016/j.biomaterials.2017.03.016. Epub 2017 Mar 11.
9
Defining the contribution of neuroinflammation to Parkinson's disease in humanized immune system mice.
Mol Neurodegener. 2017 Feb 14;12(1):17. doi: 10.1186/s13024-017-0158-z.
10
Regeneration of bone using nanoplex delivery of FGF-2 and BMP-2 genes in diaphyseal long bone radial defects in a diabetic rabbit model.
J Control Release. 2017 Feb 28;248:53-59. doi: 10.1016/j.jconrel.2017.01.008. Epub 2017 Jan 7.

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