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人唾液腺上皮细胞 2D 体外培养过程中的细胞功能和 DNA 完整性研究。

Investigation of Cellular Function and DNA Integrity during 2D in vitro Culture of Human Salivary Gland Epithelial Cells.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Klinikum Stuttgart, Stuttgart, Germany.

Department of Otorhinolaryngology, Plastic, Aesthetic, and Reconstructive Head and Neck Surgery, University Hospital Würzburg, Würzburg, Germany,

出版信息

Cells Tissues Organs. 2019;208(1-2):66-75. doi: 10.1159/000505433. Epub 2020 Feb 5.

Abstract

In vitro culture of human salivary gland epithelial cells (SGEC) is still a challenge. A high quantity and quality of cells are needed for the cultivation of 3D matrices. Furthermore, it is known that DNA damage is supposed to be an important factor involved in carcinogenesis. This study investigates cellular function and DNA integrity of human SGEC during 3 passage steps in 2 groups (group 1: n = 10; group 2: n = 9). Cellular function was analyzed by immunofluorescence, transmission electron microscopy (TEM), and quantitative real-time polymerase chain reaction (qPCR). DNA integrity was tested via the comet assay. Immunohistochemistry and qPCR results showed stable α-amylase and pan-cytokeratin levels; TEM revealed functional cells; and no significant DNA damage could be detected in the comet assay during 3 culture steps. The study shows that not only at cellular but also at DNA level human SGEC can be safely quantified over 3 passages for preclinical tissue engineering without loss of differentiation and function.

摘要

人唾液腺上皮细胞(SGEC)的体外培养仍然是一个挑战。为了培养 3D 基质,需要大量高质量的细胞。此外,已知 DNA 损伤被认为是致癌作用中的一个重要因素。本研究在 2 组(第 1 组:n = 10;第 2 组:n = 9)中研究了人 SGEC 在 3 个传代步骤中的细胞功能和 DNA 完整性。通过免疫荧光、透射电子显微镜(TEM)和实时定量聚合酶链反应(qPCR)分析细胞功能。通过彗星试验测试 DNA 完整性。免疫组织化学和 qPCR 结果显示α-淀粉酶和细胞角蛋白的水平稳定;TEM 显示功能细胞;并且在 3 个培养步骤中,彗星试验未检测到明显的 DNA 损伤。该研究表明,人 SGEC 在临床前组织工程中可以安全地进行 3 次传代,不仅在细胞水平,而且在 DNA 水平,也不会丧失分化和功能。

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