Bartolić Miha, Vovk Andrej, Šuput Dušan
Institute of Pathophysiology, Faculty of Medicine, University of Ljubljana, Zaloška cesta 4, 1000 Ljubljana, Slovenia.
Cell Mol Biol Lett. 2016 Aug 23;21:13. doi: 10.1186/s11658-016-0011-3. eCollection 2016.
Hepatic encephalopathy (HE) is a complex disorder associated with increased ammonia levels in the brain. Although astrocytes are believed to be the principal cells affected in hyperammonemia (HA), endothelial cells (ECs) may also play an important role by contributing to the vasogenic effect of HA.
Following acute application and removal of NHCl on astrocytes and endothelial cells, we analyzed pH changes, using fluorescence imaging with BCECF/AM, and changes in intracellular Ca concentration ([Ca]), employing fluorescence imaging with Fura-2/AM. Using confocal microscopy, changes in cell volume were observed accompanied by changes of [Ca] in astrocytes and ECs.
Exposure of astrocytes and ECs to 1 - 20 mM NHCl resulted in rapid concentration-dependent alkalinization of cytoplasm followed by slow recovery. Removal of the NHCl led to rapid concentration-dependent acidification, again followed by slow recovery. Following the application of NHCl, a transient, concentration-dependent rise in [Ca] in astrocytes was observed. This was due to the release of Ca from intracellular stores, since the response was abolished by emptying intracellular stores with thapsigargin and ATP, and was still present in the Ca-free bathing solution. The removal of NHCl also led to a transient concentration-dependent rise in [Ca] that resulted from Ca release from cytoplasmic proteins, since removing Ca from the bathing solution and emptying intracellular Ca stores did not eliminate the rise. Similar results were obtained from experiments on ECs. Following acute application and removal of NHCl no significant changes in astrocyte volume were detected; however, an increase of EC volume was observed after the administration of NHCl, and EC shrinkage was demonstrated after the acute removal of NHCl.
This study reveals new data which may give a more complete insight into the mechanism of development and treatment of HE.
肝性脑病(HE)是一种与脑内氨水平升高相关的复杂疾病。尽管星形胶质细胞被认为是高氨血症(HA)中受影响的主要细胞,但内皮细胞(ECs)也可能通过促成HA的血管源性效应而发挥重要作用。
在对星形胶质细胞和内皮细胞急性施加和去除氯化铵后,我们使用BCECF/AM荧光成像分析pH变化,并使用Fura-2/AM荧光成像分析细胞内钙浓度([Ca])的变化。利用共聚焦显微镜,观察到星形胶质细胞和内皮细胞中伴随着[Ca]变化的细胞体积变化。
将星形胶质细胞和内皮细胞暴露于1 - 20 mM氯化铵会导致细胞质迅速出现浓度依赖性碱化,随后缓慢恢复。去除氯化铵会导致迅速的浓度依赖性酸化,同样随后缓慢恢复。施加氯化铵后,观察到星形胶质细胞中[Ca]出现短暂的、浓度依赖性升高。这是由于细胞内储存的钙释放,因为用毒胡萝卜素和ATP排空细胞内储存会消除该反应,并且在无钙的浴液中该反应仍然存在。去除氯化铵也会导致[Ca]出现短暂的浓度依赖性升高,这是由细胞质蛋白释放钙引起的,因为从浴液中去除钙并排空细胞内钙储存并不能消除该升高。在内皮细胞实验中获得了类似结果。急性施加和去除氯化铵后,未检测到星形胶质细胞体积有显著变化;然而,施加氯化铵后观察到内皮细胞体积增加,急性去除氯化铵后证明内皮细胞收缩。
本研究揭示了新的数据,可能会更全面地洞察肝性脑病的发生发展机制和治疗方法。