Canh Minh-Y, Serpe Craig J, Sanders Virginia, Jones Kathryn J
Department of Cell Biology, Neurobiology and Anatomy Loyola University Chicago, Maywood, IL 60153, USA.
J Neuroimmunol. 2006 Dec;181(1-2):93-9. doi: 10.1016/j.jneuroim.2006.08.006. Epub 2006 Oct 11.
We have previously demonstrated that CD4(+) T cells transiently rescue facial motoneurons (FMN) from axotomy-induced death in immunodeficient mice. Three subpopulations of motoneurons have been observed within the facial motor nucleus following axotomy: one that always survives axotomy (50%), one that is amenable to rescue from axotomy-induced death through the addition of neurotrophic factors or CD4(+) T cells (30-40%), and one that always dies after axotomy (10-15%). The objective of this study was to anatomically map the extent of axotomy-induced cell death and immune cell rescue in the facial nucleus to study the differential survival capabilities of each subpopulation. Wild-type (WT) mice, recombinase activating gene 2 knockout (RAG-2 KO) mice, and RAG-2 KO mice reconstituted with CD4(+) T cells were subjected to right facial nerve axotomy. At 4 weeks post-axotomy, topographical mapping of axotomy-induced cell death throughout the rostro-caudal extent of the facial nucleus was accomplished in accordance with previously published maps of the subnuclear arrangement of the facial neurons. The results indicate that all 3 subpopulations of FMN can be found in each of the subnuclear groups throughout the entire rostro-caudal extent of the facial nucleus. These data are discussed in context of recent work in amyotrophic lateral sclerosis, a fatal motoneuron disease.
我们之前已经证明,在免疫缺陷小鼠中,CD4(+) T细胞可短暂挽救因轴突切断诱导死亡的面神经运动神经元(FMN)。轴突切断后,在面神经运动核内观察到了三类运动神经元:一类在轴突切断后始终存活(50%),一类可通过添加神经营养因子或CD4(+) T细胞挽救免于轴突切断诱导的死亡(30 - 40%),还有一类在轴突切断后总是死亡(10 - 15%)。本研究的目的是通过解剖学方法描绘面神经核内轴突切断诱导的细胞死亡范围和免疫细胞挽救情况,以研究每个亚群不同的存活能力。对野生型(WT)小鼠、重组激活基因2敲除(RAG - 2 KO)小鼠以及用CD4(+) T细胞重建的RAG - 2 KO小鼠进行右侧面神经轴突切断。在轴突切断后4周,根据先前发表的面神经神经元亚核排列图谱,完成了面神经核整个前后范围轴突切断诱导细胞死亡的地形图绘制。结果表明,在面神经核整个前后范围内的每个亚核组中都能找到所有这三类FMN亚群。本文结合肌萎缩侧索硬化症(一种致命的运动神经元疾病)的最新研究成果对这些数据进行了讨论。