[Primary culture of human gingival tissue cells in vitro].

Zhonghua ya yi xue hui za zhi Pub Date : 1991-09-01
S D Hwang, Y J Shun, C L Meng
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Abstract

In order to establish and understand the in vitro human gingival cell culture system, this study presents newly developed and characterized primary culture cell types derived from human gingival tissues. Cell cultures were established from human gingival tissues by means of the explant technique and monolayer culture. Cells were studied under stable growth conditions and were characterized in terms of their morphology, Giemsa staining, anti-epithelial cytoskeletal staining, and proliferative parameters. At confluence, disoriented fibroblast cells formed the multilayered culture. The epithelial nature of the epithelioid cells was confirmed by staining for cytoplasmic keratin which is an exclusive epithelial cell protein. The growth curve and cell doubling time of the fibroblasts were evaluated. The results indicate that both epithelial cells and fibroblasts can be cultured from human gingival tissue. This technique provides us with a stable source of normal cells for further in-depth in vitro studies.

人牙龈组织细胞的体外原代培养。
为了建立和了解人牙龈细胞体外培养体系,本研究提出了新发展的、具有特征的人牙龈组织原代培养细胞类型。采用外植体培养和单层培养的方法,从人牙龈组织中培养细胞。在稳定生长条件下研究细胞,并根据其形态学,吉姆萨染色,抗上皮细胞骨架染色和增殖参数进行表征。融合时,失向成纤维细胞形成多层培养。细胞质角蛋白染色证实了上皮样细胞的上皮性质,角蛋白是上皮细胞独有的蛋白。观察成纤维细胞的生长曲线和细胞倍增时间。结果表明,人牙龈组织上皮细胞和成纤维细胞均可培养。这项技术为我们进一步深入的体外研究提供了稳定的正常细胞来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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