高分子拥挤
增生性瘢痕
菲科尔
体内
体外
纤维连接蛋白
细胞生物学
化学
生物物理学
病理
生物
细胞外基质
医学
高分子
生物化学
遗传学
外周血单个核细胞
作者
Chen Fan,Lay Keng Priscilla Lim,Zihao Wu,Bhavya Sharma,Shi Qi Gan,Kun Liang,Zee Upton,David I. Leavesley
摘要
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.
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