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体外划痕试验以证明砷对皮肤细胞迁移的影响。

In Vitro Scratch Assay to Demonstrate Effects of Arsenic on Skin Cell Migration.

作者信息

Pinto Bronson I, Cruz Nathan D, Lujan Oscar R, Propper Catherine R, Kellar Robert S

机构信息

Department of Biological Sciences, Northern Arizona University; Center for Bioengineering Innovation, Northern Arizona University.

Department of Biological Sciences, Northern Arizona University.

出版信息

J Vis Exp. 2019 Feb 23(144). doi: 10.3791/58838.

Abstract

Understanding the physiologic mechanisms of wound healing has been the focus of ongoing research for many years. This research directly translates into changes in clinical standards used for treating wounds and decreasing morbidity and mortality for patients. Wound healing is a complex process that requires strategic cell and tissue interaction and function. One of the many critically important functions of wound healing is individual and collective cellular migration. Upon injury, various cells from the blood, surrounding connective, and epithelial tissues rapidly migrate to the wound site by way of chemical and/or physical stimuli. This migration response can largely dictate the outcomes and success of a healing wound. Understanding this specific cellular function is important for translational medicine that can lead to improved wound healing outcomes. Here, we describe a protocol used to better understand cellular migration as it pertains to wound healing, and how changes to the cellular environment can significantly alter this process. In this example study, dermal fibroblasts were grown in media supplemented with fetal bovine serum (FBS) as monolayer cultures in tissue culture flasks. Cells were aseptically transferred into tissue culture treated 12-well plates and grown to 100% confluence. Upon reaching confluence, the cells in the monolayer were vertically scratched using a p200 pipet tip. Arsenic diluted in culture media supplemented with FBS was added to individual wells at environmentally relevant doses ranging 0.1-10 M. Images were captured every 4 hours (h) over a 24 h period using an inverted light microscope to observe cellular migration (wound closure). Images were individually analyzed using image analysis software, and percent wound closure was calculated. Results demonstrate that arsenic slows down wound healing. This technique provides a rapid and inexpensive first screen for evaluation of the effects of contaminants on wound healing.

摘要

多年来,了解伤口愈合的生理机制一直是 ongoing 研究的重点。这项研究直接转化为用于治疗伤口的临床标准的变化,并降低患者的发病率和死亡率。伤口愈合是一个复杂的过程,需要细胞和组织进行战略性的相互作用和发挥功能。伤口愈合众多至关重要的功能之一是单个细胞和集体细胞的迁移。受伤后,来自血液、周围结缔组织和上皮组织的各种细胞通过化学和/或物理刺激迅速迁移到伤口部位。这种迁移反应在很大程度上可以决定愈合伤口的结果和成功率。了解这种特定的细胞功能对于可导致改善伤口愈合结果的转化医学很重要。在这里,我们描述了一种用于更好地理解与伤口愈合相关的细胞迁移以及细胞环境的变化如何能显著改变这一过程的方案。在这个示例研究中,将真皮成纤维细胞在补充有胎牛血清(FBS)的培养基中作为单层培养物在组织培养瓶中培养。将细胞无菌转移到经组织培养处理的 12 孔板中,并培养至 100%汇合。达到汇合后,使用 p200 移液器吸头垂直刮擦单层中的细胞。将在补充有 FBS 的培养基中稀释的砷以 0.1 - 10 μM 的环境相关剂量添加到各个孔中。在 24 小时内每 4 小时(h)使用倒置光学显微镜拍摄图像以观察细胞迁移(伤口闭合)。使用图像分析软件对图像进行单独分析,并计算伤口闭合百分比。结果表明砷会减缓伤口愈合。该技术为评估污染物对伤口愈合的影响提供了一种快速且廉价的初步筛选方法。

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