Hoffmann Olaf, Mahrhofer Cordula, Rueter Nina, Freyer Dorette, Bert Bettina, Fink Heidrun, Weber Joerg R
Department of Cell Biology, Center for Anatomy, Charité--Universitaetsmedizin Berlin, Schumannstr. 20/21, 10117 Berlin, Germany.
Infect Immun. 2007 Sep;75(9):4289-97. doi: 10.1128/IAI.01679-06. Epub 2007 Jun 25.
Bacterial meningitis is a major infectious cause of neuronal degeneration in the hippocampus. Neurogenesis, a continuous process in the adult hippocampus, could ameliorate such loss. Yet the high rate of sequelae from meningitis suggests that this repair mechanism is inefficient. Here we used a mouse model of nonreplicative bacterial meningitis to determine the impact of transient intracranial inflammation on adult neurogenesis. Experimental meningitis resulted in a net loss of neurons, diminished volume, and impaired neurogenesis in the dentate gyrus for weeks following recovery from the insult. Inducible nitric oxide synthase (iNOS) immunoreactivity was prominent in microglia in nonproliferating areas of the dentate gyrus and hilus region after meningitis induction. Treatment with the specific iNOS inhibitor N6-(1-iminoethyl)-L-lysine restored neurogenesis in experimental meningitis. These data suggest that local central nervous system inflammation in and of itself suppresses adult neurogenesis by affecting both proliferation and neuronal differentiation. Repair of cognitive dysfunction following meningitis could be improved by intervention to interrupt these actively suppressive effects.
细菌性脑膜炎是海马体神经元变性的主要感染性病因。神经发生是成年海马体中的一个持续过程,可改善这种损失。然而,脑膜炎后遗症的高发生率表明这种修复机制效率低下。在这里,我们使用非复制性细菌性脑膜炎小鼠模型来确定短暂性颅内炎症对成年神经发生的影响。实验性脑膜炎导致神经元净损失、体积减小,并且在损伤恢复后的数周内齿状回的神经发生受损。诱导型一氧化氮合酶(iNOS)免疫反应在脑膜炎诱导后齿状回和门区非增殖区域的小胶质细胞中显著。用特异性iNOS抑制剂N6-(1-亚氨基乙基)-L-赖氨酸治疗可恢复实验性脑膜炎中的神经发生。这些数据表明,局部中枢神经系统炎症本身通过影响增殖和神经元分化来抑制成年神经发生。通过干预中断这些积极的抑制作用,可以改善脑膜炎后认知功能障碍的修复。