Delery Elizabeth C, MacLean Andrew G
Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
Tulane Program in Biomedical Sciences, New Orleans, LA, United States.
Front Cell Neurosci. 2019 Aug 28;13:396. doi: 10.3389/fncel.2019.00396. eCollection 2019.
While there are murine and rat choroid plexus epithelial cell cultures, a translationally relevant model for choroid plexus activation and function is still lacking. The rhesus macaque is the gold standard for modeling viral infection and activation of CNS, including HIV-associated neurocognitive disorders. We have developed a rhesus macaque choroid plexus epithelial cell culture model which we believe to be suitable for studies of inflammation associated with viral infection of the CNS. Epithelial morphology and function were assessed using vimentin, phalloidin, the tight junction protein zonula-occludens-1 (ZO-1), and focal adhesion kinase (FAK). Choroid plexus epithelial cell type was confirmed using immunofluorescence with two proteins highly expressed in the choroid plexus: transthyretin and α-klotho. Finally, barrier properties of the model were monitored using pro- and anti-inflammatory mediators (TNF-α, the TLR2 agonist PamCys3K, and dexamethasone). When pro-inflammatory TNF-α was added to the xCelligence wells, there was a decrease in barrier function, which decreased in a step-wise fashion with each additional administration. This barrier function was repaired upon addition of the steroid dexamethasone. The TLR2 agonist PAM3CysK increased barrier functions in TNF-α treated wells. We have presented a model of the blood-CSF barrier that will allow study into pro- and anti-inflammatory conditions in the brain, while simultaneously measuring real time changes to epithelial cells.
虽然已有小鼠和大鼠脉络丛上皮细胞培养物,但仍缺乏与转化相关的脉络丛激活和功能模型。恒河猴是模拟病毒感染和中枢神经系统激活(包括与HIV相关的神经认知障碍)的金标准。我们开发了一种恒河猴脉络丛上皮细胞培养模型,我们认为该模型适用于研究与中枢神经系统病毒感染相关的炎症。使用波形蛋白、鬼笔环肽、紧密连接蛋白闭合蛋白-1(ZO-1)和粘着斑激酶(FAK)评估上皮形态和功能。使用在脉络丛中高度表达的两种蛋白质:转甲状腺素蛋白和α-klotho进行免疫荧光,确认脉络丛上皮细胞类型。最后,使用促炎和抗炎介质(TNF-α、TLR2激动剂PamCys3K和地塞米松)监测模型的屏障特性。当将促炎TNF-α添加到实时无标记细胞分析仪孔中时,屏障功能降低,每次额外给药时呈逐步下降趋势。添加类固醇地塞米松后,这种屏障功能得以修复。TLR2激动剂PAM3CysK增加了TNF-α处理孔中的屏障功能。我们提出了一种血脑屏障模型,该模型将允许研究大脑中的促炎和抗炎情况,同时测量上皮细胞的实时变化。