Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany; Center for Systems Neuroscience, Hannover, Germany.
Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany.
Neurobiol Dis. 2018 Feb;110:192-205. doi: 10.1016/j.nbd.2017.12.001. Epub 2017 Dec 5.
Viral encephalitis is a major risk factor for the development of seizures and epilepsy, but the underlying mechanisms are only poorly understood. Mouse models such as viral encephalitis induced by intracerebral infection with Theiler's virus in C57BL/6 (B6) mice allow advancing our understanding of the immunological and virological aspects of infection-induced seizures and their treatment. Previous studies using the Theiler's virus model in B6 mice have indicated that brain-infiltrating inflammatory macrophages and the cytokines released by these cells are key to the development of acute seizures and hippocampal damage in this model. However, approaches used to prevent or reduce macrophage infiltration were not specific, so contribution of other mechanisms could not be excluded. In the present study, we used a more selective and widely used approach for macrophage depletion, i.e., systemic administration of clodronate liposomes, to study the contribution of macrophage infiltration to development of seizures and hippocampal damage. By this approach, almost complete depletion of monocytic cells was achieved in spleen and blood of Theiler's virus infected B6 mice, which was associated with a 70% decrease in the number of brain infiltrating macrophages as assessed by flow cytometry. Significantly less clodronate liposome-treated mice exhibited seizures than liposome controls (P<0.01), but the development of hippocampal damage was not prevented or reduced. Clodronate liposome treatment did not reduce the increased Iba1 and Mac3 labeling in the hippocampus of infected mice, indicating that activated microglia may contribute to hippocampal damage. The unexpected mismatch between occurrence of seizures and hippocampal damage is thought-provoking and suggests that the mechanisms involved in degeneration of specific populations of hippocampal neurons in encephalitis-induced epilepsy are more complex than previously thought.
病毒性脑炎是癫痫发作和癫痫的主要危险因素,但潜在机制仍知之甚少。通过向 C57BL/6(B6)小鼠的脑内感染 Theiler 病毒诱导病毒性脑炎的小鼠模型,如 Theiler 病毒诱导的病毒性脑炎模型,使我们能够深入了解感染诱导的癫痫发作及其治疗的免疫学和病毒学方面。先前使用 B6 小鼠中的 Theiler 病毒模型的研究表明,脑内浸润的炎症性巨噬细胞和这些细胞释放的细胞因子是该模型中急性癫痫发作和海马损伤发展的关键。然而,用于预防或减少巨噬细胞浸润的方法并不具有特异性,因此不能排除其他机制的贡献。在本研究中,我们使用了一种更具选择性和广泛使用的巨噬细胞耗竭方法,即系统给予氯膦酸盐脂质体,以研究巨噬细胞浸润对癫痫发作和海马损伤发展的贡献。通过这种方法,在 Theiler 病毒感染的 B6 小鼠的脾脏和血液中几乎完全耗尽了单核细胞,这与通过流式细胞术评估的脑内浸润巨噬细胞数量减少了 70%相关。与脂质体对照相比,接受氯膦酸盐脂质体治疗的小鼠明显更少发生癫痫发作(P<0.01),但未预防或减轻海马损伤的发展。氯膦酸盐脂质体治疗并未减少感染小鼠海马中 Iba1 和 Mac3 标记的增加,表明活化的小胶质细胞可能有助于海马损伤。癫痫发作和海马损伤的发生之间出乎意料的不匹配令人深思,这表明在脑炎诱导的癫痫中特定海马神经元群体退化所涉及的机制比以前认为的更为复杂。