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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Squid type II collagen as a novel biomaterial: Isolation, characterization, immunogenicity and relieving effect on degenerative osteoarthritis via inhibiting STAT1 signaling in pro-inflammatory macrophages
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Squid type II collagen as a novel biomaterial: Isolation, characterization, immunogenicity and relieving effect on degenerative osteoarthritis via inhibiting STAT1 signaling in pro-inflammatory macrophages

机译:鱿鱼II型胶原蛋白作为一种新型生物材料:通过抑制促炎巨噬细胞抑制STAT1信号传导来分离,表征,免疫原性对退化性骨关节炎的影响

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摘要

Collagen from marine organisms has a broad prospect in biomedical field, yet the knowledge on marine-derived type II collagen is rare. Herein, a novel type II collagen was successfully isolated from squid cartilage for the first time. After being characterized, the immunogenicity of squid type II collagen (SCII) was evaluated and compared with that of bovine type II collagen (BCII). Then investigations were further conducted for the impacts of SCII on pro-inflammatory macrophages and macrophage chemotaxis. The degenerative osteoarthritis (OA)-relieving effects of SCII were explored using OA rat model in vivo. Our results demonstrated that the isolated SCII maintained triple-superhelical structure of native collagen with high purity. Different from BCII, SCII presented no immunogenicity since it neither induced abnormal proliferation of lymphocytes in vitro nor changed the basic levels of IgM, IgG, anti-type II collagen IgG and CD4(+)/CD8(+) lymphocytes ratio in vivo. Additionally, SCII also exerted prominent anti-inflammatory effects. SCII significantly reduced the production of pro-inflammatory cytokines by enhancing the activity of TCPTP and subsequently prompting the dephosphorylation of p-STAT1 in pro-inflammatory macrophages. Besides, it indirectly prevented hypertrophic changes of chondrocytes, and markedly impeded chemotaxis of macrophages. Moreover, inflammation condition in OA rats was significantly alleviated under treatment with SCII. These data suggested that the newly developed SCII could not only avoid the immunogenic risks of collagen derived from terrestrial animals, but more importantly, provide new choice for the control and treatment of OA.
机译:来自海洋生物的胶原蛋白在生物医学领域具有广阔的前景,但海洋衍生II型胶原蛋白的知识是罕见的。在此,首次从鱿鱼软骨中成功地分离出一种新型II型胶原蛋白。其特征在于,评价鱿鱼II型胶原(SCII)的免疫原性,并与牛II型胶原(BCII)进行比较。然后进一步调查SCII对促炎巨噬细胞和巨噬细胞趋化性的影响。在体内使用OA RAT模型探讨了SCII的退行性骨关节炎(OA)的影响。我们的结果表明,隔离的SCII维持了具有高纯度的天然胶原的三倍 - 超级结构。与BCII不同,SCII没有呈免疫原性,因为它既不诱导体外淋巴细胞异常增殖也不改变IgM,IgG,抗型II胶原IgG和CD4(+)/ CD8(+)淋巴细胞比例的基本水平。此外,SCII还施加了突出的抗炎作用。 SCII通过增强TCPT的活性并随后提示在促炎巨噬细胞中的P-Stat1的去磷酸化进行促炎细胞因子的产生。此外,它间接地防止了软骨细胞的肥厚变化,并显着阻碍了巨噬细胞的趋化性。此外,用SCII治疗,OA大鼠的炎症状况显着缓解。这些数据表明,新开发的SCII不仅可以避免源自陆地动物的胶原蛋白的免疫原性风险,但更重要的是,为OA的控制和治疗提供新的选择。

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