血液暴露、儿茶酚胺水平升高和炎症介质对体外脑微血管内皮细胞完整性的影响

M. Smetak, Cora Ittner, M. Burek, M. Nagai, C. Förster
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摘要

导语:最近的研究表明,儿茶酚胺和炎症介质INF对血液的影响会影响血脑屏障(BBB)的完整性,特别是当合并出血性中风时,这种情况在Taktosubo综合征TTS中经常观察到。我们在体外研究了这些应激源对脑微血管内皮的可能影响。方法:采用永生化小鼠大脑皮层微血管内皮细胞系(cEND)作为血脑屏障的体外模型。用含有应激因子(如儿茶酚胺、TNF-α和白细胞介素-6)超生理浓度的患者血液(如急性takotsubo综合征TTS患者血液中的特征性升高)处理cEND。我们通过光镜和免疫荧光染色研究了对单层完整性和细胞形态的影响。此外,通过RT-PCR和/或Western Blot检测代表性紧密和粘附连接蛋白以及整合素的变化。结果:经应激因子/患者血液处理后,体外观察到脑毛细血管内皮细胞活力降低。通过实时RT-PCR (qPCR)、western blot和免疫荧光标记检测,这伴随着细胞单层完整性的破坏和形成血脑屏障紧密连接蛋白的定位改变。此外,通过测量跨内皮电阻来确定单层的完整性。结论:暴露于患者血液、儿茶酚胺CAT和炎症介质INF分别明显影响形成血脑屏障的细胞单层完整性和蛋白质表达。大多数屏障蛋白下调,因此可以假设对形成血脑屏障的脑内皮细胞有负面影响。
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Effects of blood exposure, increased catecholamine levels and inflammatory mediators on brain microvascular endothelial cell integrity in vitro
Introduction: Recent studies have suggested the impact of increased catecholamine levels CAT and inflammatory mediators INF on blood on the integrity of the blood brain barrier (BBB), especially when occurring in combination with hemorrhagic stroke, a situation frequently observed in Taktosubo syndrome TTS. We investigated the possible effects of these stressors on the brain microvascular endothelium in vitro. Methods: As an in vitro model of the BBB we used an immortalized murine microvascular endothelial cell line from the cerebral cortex (cEND). The cEND were treated with medium or patient blood containing supraphysiological concentrations of stress factors such as catecholamines, TNF-α and Interleukin-6 as characteristically elevated in patient blood  suffering from acute takotsubo syndrome TTS. We investigated the impact on monolayer integrity and cellular morphology by light microscopy and immunofluorescence staining. Furthermore, alterations of representative tight and adherence junction proteins as well as integrins were determined by RT-PCR and/or Western Blot. Results: After stress factor/ patient blood treatment, reduced viability of brain capillary endothelial cells in vitro was observed. This was concomitant with a disruption of cellular monolayer integrity and changed localisation of BBB-forming tight junction proteins as determined by real-time RT-PCR (qPCR), western blot and immunofluorescence labeling. Monolayer integrity was moreover determined by measurement of transendothelial electrical resistance. Conclusion: Cellular monolayer integrity and the expression of proteins forming the BBB are clearly affected by exposure to patient blood, catecholamines CAT and inflammatory mediators INF, respectively. Most of barrier proteins are downregulated, so a negative impact on brain endothelial cells forming the blood-brain barrier can be assumed.
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