成纤维细胞嵌入三维胶原作为上皮伤口修复的潜在工具

Claire Behning, Lia Kelly, Emma Smith, Yizhe Ma, Louis Roberts
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引用次数: 0

摘要

胶原蛋白是一种功能性生物材料,应用广泛,包括伤口愈合。三维胶原蛋白水凝胶可模拟用于细胞存活和生长研究的体内细胞培养体验。通过实验研究与三维胶原接触的人体细胞,可以了解胶原在人体上皮组织修复中的作用。本研究通过研究嵌入胶原蛋白中的 NIH/3T3 成纤维细胞是否会产生更强的伤口愈合反应,来探索人类 MCF-7 细胞暴露于三维胶原蛋白时的生长和附着反应。三维胶原蛋白和成纤维细胞的存在可与凝胶的 "三明治 "结构一起分析,以确定这些变量如何影响或改善 MCF-7 细胞的组织修复反应。对生长、附着、存活率和迁移模式的研究表明,当 MCF-7 细胞与 NIH/3T3 嵌入式三维胶原接触时,其修复反应可能会增强,而不会影响存活率。最值得注意的是,迁移试验结果表明,MCF-7 细胞被细胞三维胶原覆盖和附着时迁移率最高。MCF-7细胞顶部和下方的成纤维细胞包埋胶原蛋白超过了定量评估,达到了接近汇合的程度,而在没有任何顶部胶原蛋白分层的情况下,每张图片上的细胞迁移数量不足50个。要继续使用这些方法,可以结合活体动物模型进行体内实验,以确定这些结果是否会继续扩展到活体组织。关键词: 胶原;三维胶原;成纤维细胞;伤口愈合;水凝胶;组织修复;迁移
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fibroblast Embedded 3D Collagen as a Potential Tool for Epithelial Wound Repair
Collagen is a functional biomaterial with many applications, including wound healing. 3D collagen hydrogels mimic an in vivo cell culture experience used in cell survival and growth studies. In experimentally examining human cells under contact with 3D collagen, it is possible to understand the role of collagen in human epithelial tissue repair. This study explored the growth and attachment response of human MCF-7 cells when exposed to 3D collagen by investigating if the presence of NIH/3T3 fibroblasts embedded within the collagen should produce an increased wound-healing response. 3D collagen and fibroblast presence were able to be analyzed in tandem with a “sandwich-like” configuration of the gels to determine how these variables impact or improve the tissue repair response in MCF-7 cells. Examinations in growth, attachment, viability, and migration patterns demonstrated that MCF-7 repair response may be increased when in contact with NIH/3T3 embedded 3D collagen without impairing viability. Most notably, results from the migration assay revealed that MCF-7 cells migrate the most when covered by and adhered to cellular 3D collagen. Fibroblast-embedded collagen on top of and below MCF-7 cells exceeded quantitative assessment to near confluency, whereas less than 50 counted cells per image migrated without any top collagen layering. The continuation of these methods could involve in vivo experiments that incorporate live animal models to determine if these results will continue to extend to live tissue. KEYWORDS: Collagen; 3D Collagen; Fibroblasts; Wound Healing; Hydrogels; Tissue Repair; Migration
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