Fan Chen, Lim Lay Keng Priscilla, Wu Zihao, Sharma Bhavya, Gan Shi Qi, Liang Kun, Upton Zee, Leavesley David
Skin Research Institute of Singapore, Agency for Science, Technology and Research (A*STAR);
Skin Research Institute of Singapore, Agency for Science, Technology and Research (A*STAR).
J Vis Exp. 2020 May 1(159). doi: 10.3791/61037.
It has been shown that in vivo tissues are highly crowded by proteins, nucleic acids, ribonucleoproteins, polysaccharides, etc. The following protocol applies a macromolecular crowding (MMC) technique to mimic this physiological crowding through the addition of neutral polymers (crowders) to cell cultures in vitro. Previous studies using Ficoll or dextran as crowders demonstrate that the expression of collagen I and fibronectin in WI38 and WS-1 cell lines are significantly enhanced using the MMC technique. However, this technique has not been validated in primary hypertrophic scar-derived human skin fibroblasts (hHSFs). As hypertrophic scarring arises from the excessive deposition of collagen, this protocol aims to construct a collagen-rich in vitro hypertrophic scar model by applying the MMC technique with hHSFs. This optimized MMC model has been shown to possess more similarities with in vivo scar tissue compared to traditional 2-dimensional (2-D) cell culture systems. In addition, it is cost-effective, time-efficient, and ethically desirable compared to animal models. Therefore, the optimized model reported here offers an advanced "in vivo-like" model for hypertrophic scar-related studies.
研究表明,体内组织被蛋白质、核酸、核糖核蛋白、多糖等高度拥挤。以下方案应用大分子拥挤(MMC)技术,通过向体外细胞培养物中添加中性聚合物(拥挤剂)来模拟这种生理拥挤。先前使用Ficoll或右旋糖酐作为拥挤剂的研究表明,使用MMC技术可显著增强WI38和WS-1细胞系中I型胶原蛋白和纤连蛋白的表达。然而,该技术尚未在原发性肥厚性瘢痕来源的人皮肤成纤维细胞(hHSF)中得到验证。由于肥厚性瘢痕形成源于胶原蛋白的过度沉积,本方案旨在通过对hHSF应用MMC技术构建富含胶原蛋白的体外肥厚性瘢痕模型。与传统的二维(2-D)细胞培养系统相比,这种优化的MMC模型已被证明与体内瘢痕组织具有更多相似性。此外,与动物模型相比,它具有成本效益高、省时且符合伦理要求的特点。因此,本文报道的优化模型为肥厚性瘢痕相关研究提供了一种先进的“类体内”模型。