增强免疫调节的内源性双响应自适应丝素蛋白支架用于颅骨再生

IF 12.8 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Xuewei Bi , Zhinan Mao , Yilin Zhang , Zeqi Ren , Kang Yang , Chunhao Yu , Lei Chen , Rui Zheng , Juan Guan , Zhenhai Liu , Binsheng Yu , Yongcan Huang , Xiong Shu , Yufeng Zheng
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引用次数: 0

摘要

尽管目前生物材料(如钛网、聚醚醚酮)已应用于临床颅骨修复,但其在力学匹配、形状适应性、生物活性和骨整合等方面的局限性极大地限制了其临床应用。本研究以基质金属蛋白酶-2响应明胶-甲基丙烯酰-白细胞介素-4 (IL-4)为涂层,构建了一种基于水和炎症微环境双响应的自适应丝素-氧化镁支架,该支架具有良好的机械顺应性、快速的形状匹配性和术中可再加工性。具有免疫活性的IL-4和Mg2+结合能够通过抑制糖酵解、促进线粒体氧化磷酸化和调节巨噬细胞中腺苷5′-单磷酸活化蛋白激酶(AMPK)信号通路,协同促进代谢重编程,从而显著促进M2巨噬细胞的激活。在组织重构阶段,Mg2+的持续释放进一步促进巨噬细胞M2极化和抗炎细胞因子的表达,显著降低免疫应答,提高异位成骨能力。同时,通过对雄性大鼠颅骨缺损模型的研究表明,该支架能够显著增强生物矿化沉积和血管化,实现颅骨缺损的良好骨再生。总之,生物活性支架为修复临界尺寸颅骨缺损提供了一种有前途的生物材料和替代修复策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Endogenous dual-responsive and self-adaptive silk fibroin-based scaffold with enhancement of immunomodulation for skull regeneration

Endogenous dual-responsive and self-adaptive silk fibroin-based scaffold with enhancement of immunomodulation for skull regeneration
Despite the current biomaterials (e.g. titanium mesh and polyether ether ketone) have been applied to clinical skull repair, the limitations on mechanical match, shape adaptability, bioactivity and osteointegration have greatly limited their clinical application. In this work, we constructed a water and inflammatory microenvironment dual-responsive self-adaptive silk fibroin-magnesium oxide-based scaffold with the matrix metalloproteinase-2-responsive gelatin-methacryloyl-interleukin-4 (IL-4) coating, which presented good mechanical compliance, quickly shape matching and intraoperative reprocessability. With the capability of responding to an acute inflammation microenvironment followed by a triggered on-demand release of the IL-4, the combination of immunoactive IL-4 and Mg2+ co-ordinately facilitated metabolic reprogramming by suppressing glycolysis, promoting mitochondrial oxidative phosphorylation and modulating adenosine 5′-monophosphate-activated protein kinase (AMPK) signalling pathways in macrophages, resulting in significantly facilitating M2 macrophage activation. During the stage of tissue remodelling, the sustained release of Mg2+ further promoted macrophage M2 polarization and the expression of anti-inflammatory cytokines, significantly reduced immune response and improved ectopic osteogenesis ability. Meanwhile, the cranial defect models of male rats demonstrated that this scaffold could significantly enhance biomineralized deposition and vascularisation, and achieve good bone regeneration of cranial defects. Overall, the bioactive scaffold provides a promising biomaterial and alternative repair strategy for critical-size skull defect repair.
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来源期刊
Biomaterials
Biomaterials 工程技术-材料科学:生物材料
CiteScore
26.00
自引率
2.90%
发文量
565
审稿时长
46 days
期刊介绍: Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.
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