Isolation and Culture of Primary Human Gingival Epithelial Cells using Y-27632

外植体培养 上皮 体外 细胞生物学 再生(生物学) 细胞培养 组织培养 生物 化学 病理 医学 生物化学 遗传学
作者
Zhiwei Xie,Jizhou Shi,Min Zong,Qiuping Xu,Chang Liu,Jie Wen,Qun Zhang,Panpan Liu,Guanyi Liu,Jing Guo,Xunwei Wu
出处
期刊:Journal of Visualized Experiments [MyJoVE Corporation]
卷期号: (177) 被引量:3
标识
DOI:10.3791/62978
摘要

The gingival tissue is the first structure that protects periodontal tissues and plays meaningful roles in many oral functions. The gingival epithelium is an important structure of gingival tissue, especially in the repair and regeneration of periodontal tissue. Studying the functions of gingival epithelial cells has crucial scientific value, such as repairing oral defects and detecting the compatibility of biomaterials. As human gingival epithelial cells are highly differentiated keratinized cells, their lifespan is short, and they are difficult to passage. So far, there are only two ways to isolate and culture gingival epithelial cells, a direct explant method and an enzymatic method. However, the time required to obtain epithelial cells using the direct explant method is longer, and the cell survival rate of the enzymatic method is lower. Clinically, the acquisition of gingival tissue is limited, so a stable, efficient, and simple in vitro isolation and culture system is needed. We improved the traditional enzymatic method by adding Y-27632, a Rho-associated kinase (ROCK) inhibitor, which can selectively promote the growth of epithelial cells. Our modified enzymatic method simplifies the steps of the traditional enzymatic method and increases the efficiency of culturing epithelial cells, which has significant advantages over the direct explant method and the enzymatic method.
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