School of Biochemistry, Biomedical Sciences Building, University Walk, University of Bristol, Bristol BS8 1TD, United Kingdom.
Department Oral and Maxillofacial Surgery, University Hospitals Bristol, Lower Maudlin Street, Bristol BS1 2LY, UK.
J Cell Sci. 2019 Sep 26;133(5):jcs236075. doi: 10.1242/jcs.236075.
Implanting biomaterials in tissues leads to inflammation and a foreign body response (FBR), which can result in rejection. Here, we live image the FBR triggered by surgical suture implantation in a translucent zebrafish model and compare with an acute wound response. We observe inflammation extending from the suture margins, correlating with subsequent avascular and fibrotic encapsulation zones: sutures that induce more inflammation result in increased zones of avascularity and fibrosis. Moreover, we capture macrophages as they fuse to become multinucleate foreign body giant cells (FBGCs) adjacent to the most pro-inflammatory sutures. Genetic and pharmacological dampening of the inflammatory response minimises the FBR (including FBGC generation) and normalises the status of the tissue surrounding these sutures. This model of FBR in adult zebrafish allows us to live image the process and to modulate it in ways that may lead us towards new strategies to ameliorate and circumvent FBR in humans.This article has an associated First Person interview with the first author of the paper.
将生物材料植入组织会引发炎症和异物反应(FBR),从而导致排斥反应。在这里,我们通过半透明斑马鱼模型实时成像研究了手术缝线植入引发的 FBR,并将其与急性创伤反应进行了比较。我们观察到炎症从缝线边缘扩散,与随后的无血管和纤维囊形成区相关联:引起更多炎症的缝线会导致无血管区和纤维化区增加。此外,我们还捕捉到了巨噬细胞融合成多核异物巨细胞(FBGC),这些细胞紧邻最具炎症性的缝线。通过遗传和药理学抑制炎症反应,可最大限度地减少 FBR(包括 FBGC 的生成)并使缝线周围组织的状态正常化。这种成年斑马鱼的 FBR 模型使我们能够实时成像该过程,并以可能为改善和规避人类 FBR 提供新策略的方式对其进行调节。本文有一篇与该论文第一作者的第一人称访谈。