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利用八目鳗粘液中间丝蛋白构建仿生布鲁赫膜模型。

Engineering a Biomimetic Model of Bruch's Membrane Using Hagfish Slime Intermediate Filament Proteins.

机构信息

Department of Biological Engineering, Utah State University, 4105 Old Main Hill, Logan, Utah 84322-4105 United States.

Department of Biology, Utah State University, 5305 Old Main Hill, Logan, Utah 84322-5305, United States.

出版信息

ACS Biomater Sci Eng. 2023 Aug 14;9(8):5051-5061. doi: 10.1021/acsbiomaterials.3c00411. Epub 2023 Jul 17.

Abstract

Bruch's membrane resides in the subretinal tissue and regulates the flow of nutrients and waste between the retinal pigment epithelial (RPE) and vascular layers of the eye. With age, Bruch's membrane becomes thicker, stiffer, and less permeable, which impedes its function as a boundary layer in the subretina. These changes contribute to pathologies such as age-related macular degeneration (AMD). To better understand how aging in Bruch's membrane affects surrounding tissues and to determine the relationship between aging and disease, an model of Bruch's membrane is needed. An accurate model of Bruch's membrane must be a proteinaceous, semipermeable, and nonporous biomaterial with similar mechanical properties to conditions. Additionally, this model must support RPE cell growth. While models of subretinal tissue exist, they typically differ from Bruch's membrane in one or more of these properties. This study evaluates the capability of membranes created from recombinant hagfish intermediate filament (rHIF) proteins to accurately replicate Bruch's membrane in an model of the subretinal tissue. The physical characteristics of these rHIF membranes were evaluated using mechanical testing, permeability assays, brightfield microscopy, and scanning electron microscopy. The capacity of the membranes to support RPE cell culture was determined using brightfield and fluorescent microscopy, as well as immunocytochemical staining. This study demonstrates that rHIF protein membranes are an appropriate biomaterial to accurately mimic both healthy and aged Bruch's membrane for modeling of the subretinal tissue.

摘要

Bruch 膜位于视网膜下组织中,调节视网膜色素上皮(RPE)和眼部血管层之间的营养物质和废物的流动。随着年龄的增长,Bruch 膜变得更厚、更硬、渗透性更低,这阻碍了它作为视网膜下边界层的功能。这些变化导致了年龄相关性黄斑变性(AMD)等疾病。为了更好地了解 Bruch 膜的衰老如何影响周围组织,并确定衰老与疾病之间的关系,需要建立 Bruch 膜模型。一个准确的 Bruch 膜模型必须是一种具有蛋白质、半透性和非多孔性的生物材料,具有与生理条件相似的机械性能。此外,该模型必须支持 RPE 细胞的生长。虽然存在视网膜下组织模型,但它们在这些特性中的一个或多个方面通常与生理 Bruch 膜不同。本研究评估了来源于重组八目鳗中间丝(rHIF)蛋白的膜在视网膜下组织的生理模型中准确复制 Bruch 膜的能力。使用机械测试、渗透性测定、明场显微镜和扫描电子显微镜评估了这些 rHIF 膜的物理特性。通过明场和荧光显微镜以及免疫细胞化学染色来确定膜支持 RPE 细胞培养的能力。本研究表明,rHIF 蛋白膜是一种合适的生物材料,可以准确模拟生理视网膜下组织的健康和衰老的 Bruch 膜。

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