Jiao Jian, Meng Na, Wang Hong, Zhang Luo
Department of Otolaryngology, Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing, 100005, China.
Front Med. 2013 Dec;7(4):486-91. doi: 10.1007/s11684-013-0287-x. Epub 2013 Sep 5.
The purpose of this study was to compare cell growth characteristics, ciliated cell differentiation, and function of human nasal epithelial cells established as explant outgrowth cultures or dissociated tissue cultures. Human nasal mucosa of the uncinate process was obtained by endoscopy and epithelial cell cultures were established by explant outgrowth or dissociated tissue culture methods. Epithelial cell growth characteristics were observed by inverted phase contrast microscopy. Ciliated cell differentiation was detected by β-tubulin IVand ZO-1 immunocytochemistry. Basal and ATP-stimulated ciliary beat frequency (CBF) was measured using a highspeed digital microscopic imaging system. Both the explant and dissociated tissue cultures established as monolayers with tight junctions and differentiated cell composition, with both types of cultures comprising ciliated and non-ciliated epithelial cells. Fibroblasts were also frequently found in explant cultures but rarely seen in dissociated tissue cultures. In both culture systems, the highest ciliated cell density appeared at 7th-10th culture day and declined with time, with the lifespan of ciliated cells ranging from 14 to 21 days. Overall, 10% of the cells in explant cultures and 20% of the cells in the dissociated tissue cultures were ciliated. These two cultures demonstrated similar ciliary beat frequency values at baseline (7.78 ± 1.99 Hz and 7.91 ± 2.52 Hz, respectively) and reacted equivalently following stimulation with 100 μM ATP. The results of this study indicate that both the explant outgrowth and dissociated tissue culture techniques are suitable for growing well-differentiated nasal ciliated and non-ciliated cells, which have growth characteristics and ciliary activity similar to those of nasal epithelial cells in vivo.
本研究的目的是比较通过外植体生长培养或解离组织培养建立的人鼻上皮细胞的细胞生长特性、纤毛细胞分化及功能。通过内窥镜获取钩突的人鼻黏膜,并采用外植体生长或解离组织培养方法建立上皮细胞培养物。通过倒置相差显微镜观察上皮细胞生长特性。采用β -微管蛋白IV和紧密连接蛋白1(ZO - 1)免疫细胞化学检测纤毛细胞分化。使用高速数字显微成像系统测量基础和ATP刺激后的纤毛摆动频率(CBF)。外植体培养物和解离组织培养物均形成具有紧密连接和分化细胞组成的单层,两种培养物均包含纤毛和非纤毛上皮细胞。在外植体培养物中也经常发现成纤维细胞,但在解离组织培养物中很少见。在两种培养系统中,最高纤毛细胞密度出现在培养的第7至10天,并随时间下降,纤毛细胞的寿命为14至21天。总体而言,外植体培养物中10%的细胞和解离组织培养物中20%的细胞为纤毛细胞。这两种培养物在基线时显示出相似的纤毛摆动频率值(分别为7.78±1.99Hz和7.91±2.52Hz),并且在100μM ATP刺激后反应相当。本研究结果表明,外植体生长和解离组织培养技术均适用于培养分化良好的鼻纤毛和非纤毛细胞,这些细胞具有与体内鼻上皮细胞相似的生长特性和纤毛活性。