Park Do Yang, Kim Sujin, Kim Chang Hoon, Yoon Joo Heon, Kim Hyun Jik
Department of Otolaryngology-Head and Neck Surgery, Soonchunhyang University College of Medicine, Cheonan Hospital, Cheonan, Korea.
BK21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
Allergy Asthma Immunol Res. 2016 Jan;8(1):69-78. doi: 10.4168/aair.2016.8.1.69. Epub 2015 Sep 16.
Although differentiated normal human nasal epithelial (NHNE) cells can be used to study the role of human nasal epithelium, there is a need for effective culture models of nasal epithelium in sinonasal disease status, including allergic rhinitis (AR). We aimed to examine the feasibility of intranasal brushing for culture of nasal epithelial cells in AR patients and to verify the hypothesis that allergic nasal epithelial (ARNE) cells differ in histologic and physiologic characteristics.
We established a system for isolating (via intranasal brushing) and culturing (with air-liquid interface, ALI) nasal epithelial cells from healthy volunteers (n=8) and AR patients (n=8). We used this system to compare the histologic findings and physiologic characteristics of NHNE and ARNE.
The histology results showed that fully differentiated ALI culture was obtained at least 14 days after confluence and that both ciliated and secretory cells were well differentiated in ALI culture using nasal brushing. The histology results of ARNE culture were significantly different from NHNE. The number of ciliated cells was lower, and secretory cells were more dominant in ARNE cell culture compared to NHNE cells. We also observed, by electron microscopy, loose tight junctions and short cilia in cultured ARNE cells. In addition, the mRNA level of TSLP which was one of the epithelial-derived allergic cytokines was significantly higher, and the expressions of genes involved in ciliogenesis were lower in cultured ARNE cells without allergen stimulation.
Our findings suggest that ALI culture of ARNE cells using intranasal brushing may be an alternative method for epithelial cell culture in AR patients and that cultured ARNE cells will be useful for in vitro studies of the mechanisms at play during AR because they maintain unique allergic characteristics.
尽管分化的正常人鼻上皮(NHNE)细胞可用于研究人鼻上皮的作用,但仍需要针对鼻窦疾病状态(包括过敏性鼻炎(AR))建立有效的鼻上皮细胞培养模型。我们旨在探讨经鼻刷取法培养AR患者鼻上皮细胞的可行性,并验证变应性鼻上皮(ARNE)细胞在组织学和生理学特征上存在差异这一假设。
我们建立了一个从健康志愿者(n = 8)和AR患者(n = 8)中分离(通过经鼻刷取)和培养(气液界面,ALI)鼻上皮细胞的系统。我们使用该系统比较NHNE和ARNE的组织学结果和生理学特征。
组织学结果显示,汇合后至少14天可获得完全分化的ALI培养物,并且使用经鼻刷取法在ALI培养中纤毛细胞和分泌细胞均分化良好。ARNE培养的组织学结果与NHNE有显著差异。与NHNE细胞相比,ARNE细胞培养中纤毛细胞数量较少,分泌细胞更为占优势。我们还通过电子显微镜观察到,培养的ARNE细胞中紧密连接松散且纤毛较短。此外,在未受过敏原刺激的培养ARNE细胞中,上皮源性变应性细胞因子之一的TSLP的mRNA水平显著更高,而参与纤毛发生的基因表达较低。
我们的研究结果表明,经鼻刷取法对ARNE细胞进行ALI培养可能是AR患者上皮细胞培养的一种替代方法,并且培养的ARNE细胞对于AR发病机制的体外研究将是有用的,因为它们保持了独特的变应性特征。