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海洋来源的胶原蛋白和明胶提取物的免疫反应研究及其在组织工程中的应用。

Study of the immunologic response of marine-derived collagen and gelatin extracts for tissue engineering applications.

机构信息

3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017, Barco, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal.

ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal; Life and Health Sciences Research Institute, School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.

出版信息

Acta Biomater. 2022 Mar 15;141:123-131. doi: 10.1016/j.actbio.2022.01.009. Epub 2022 Jan 10.

Abstract

The host immunologic response to a specific material is a critical aspect when considering it for clinical implementation. Collagen and gelatin extracted from marine sources have been proposed as biomaterials for tissue engineering applications, but there is a lack of information in the literature about their immunogenicity. In this work, we evaluated the immune response to collagen and/or gelatin from blue shark and codfish, previously extracted and characterized. After endotoxin evaluation, bone marrow-derived macrophages were exposed to the materials and a panel of pro- and anti-inflammatory cytokines were evaluated both for protein quantification and gene expression. Then, the impact of those materials in the host was evaluated through peritoneal injection in C57BL/6 mice. The results suggested shark collagen as the less immunogenic material, inducing low expression of pro-inflammatory cytokines as well as inducible nitric oxide synthase (encoded by Nos2) and high expression of Arginase 1 (encoded by Arg1). Although shark gelatin appeared to be the material with higher pro-inflammatory expression, it also presents a high expression of IL-10 (anti-inflammatory cytokine) and Arginase (both markers for M2-like macrophages). When injected in the peritoneal cavity of mice, our materials demonstrated a transient recruitment of neutrophil, being almost non-existent after 24 hours of injection. Based on these findings, the studied collagenous materials can be considered interesting biomaterial candidates for regenerative medicine as they may induce an activation of the M2-like macrophage population, which is involved in suppressing the inflammatory processes promoting tissue remodeling. STATEMENT OF SIGNIFICANCE: Marine-origin biomaterials are emerging in the biomedical arena, namely the ones based in marine-derived collagen/gelatin proposed as cell templates for tissue regeneration. Nevertheless, although the major cause of implant rejection in clinical practice is the host's negative immune response, there is a lack of information in the literature about the immunological impact of these marine collagenous materials. This work aims to contribute with knowledge about the immunologic response to collagen/gelatin extracted from blue shark and codfish skins. The results demonstrated that despite some differences observed, all the materials can induce a macrophage phenotype related with anti-inflammation resolution and then act as immuno-modulators and anti-inflammatory inducible materials.

摘要

当考虑将某种材料用于临床应用时,宿主的免疫反应是一个关键方面。从海洋来源提取的胶原和明胶已被提议作为组织工程应用的生物材料,但文献中缺乏关于它们免疫原性的信息。在这项工作中,我们评估了从蓝鲨和鳕鱼中提取和表征的胶原和/或明胶的免疫反应。在评估内毒素后,骨髓来源的巨噬细胞暴露于这些材料,并评估了一系列促炎和抗炎细胞因子的蛋白定量和基因表达。然后,通过向 C57BL/6 小鼠腹腔注射这些材料来评估它们对宿主的影响。结果表明,鲨鱼胶原是免疫原性较低的材料,诱导低表达促炎细胞因子以及诱导型一氧化氮合酶(由 Nos2 编码)和精氨酸酶 1(由 Arg1 编码)的高表达。尽管鲨鱼明胶似乎是具有更高促炎表达的材料,但它也表现出高表达的白细胞介素 10(抗炎细胞因子)和精氨酸酶(两者均为 M2 样巨噬细胞的标志物)。当将这些材料注入小鼠腹腔时,我们的材料在 24 小时内仅短暂地招募了中性粒细胞,几乎不存在。基于这些发现,所研究的胶原类材料可以被认为是再生医学中有趣的生物材料候选物,因为它们可以诱导 M2 样巨噬细胞群体的激活,该群体参与抑制促组织重塑的炎症过程。意义声明:海洋来源的生物材料正在生物医学领域崭露头角,特别是基于海洋衍生胶原/明胶的生物材料,它们被提议作为组织再生的细胞模板。然而,尽管在临床实践中植入物排斥的主要原因是宿主的负面免疫反应,但文献中缺乏关于这些海洋胶原材料免疫影响的信息。这项工作旨在为从蓝鲨和鳕鱼皮中提取的胶原/明胶的免疫反应提供知识。结果表明,尽管观察到一些差异,但所有材料都可以诱导与抗炎消退相关的巨噬细胞表型,从而作为免疫调节剂和抗炎诱导材料发挥作用。

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