DeBoy Cynthia A, Byram Susanna C, Serpe Craig J, Wisuri Danielle, Sanders Virginia M, Jones Kathryn J
Department of Cell Biology, Neurobiology, and Anatomy, Loyola University Chicago, Maywood, IL 60153, and Research and Development Service, Hines VA Hospital 60141, USA.
J Neuroimmunol. 2006 Jul;176(1-2):34-8. doi: 10.1016/j.jneuroim.2006.04.006.
CD4+ T cells rescue facial motoneurons (FMN) from axotomy-induced cell death. The objective of this study is to determine if the CD4+ T regulatory subsets, CD4+CD25+ T or CD1d-restricted NKT cells are critical for FMN survival after facial nerve axotomy. Surviving FMN within facial motor nuclei from axotomized and control sides 4 weeks after axotomy were counted to determine percent FMN survival. Data generated by applying this paradigm to recombination activating gene-2-deficient mice reconstituted with CD4+ T cells depleted of CD4+CD25+ T cells and to CD1-/- mice, deficient in CD1d-restricted NKT cells, suggest that neither regulatory CD4+ T subset is critical for FMN survival.
CD4+ T细胞可挽救因轴突切断诱导的面运动神经元(FMN)死亡。本研究的目的是确定CD4+ T调节亚群,即CD4+CD25+ T细胞或CD1d限制性自然杀伤T(NKT)细胞,对面神经轴突切断后FMN存活是否至关重要。在轴突切断4周后,对切断侧和对照侧面部运动核内存活的FMN进行计数,以确定FMN存活百分比。通过将该范式应用于用耗尽CD4+CD25+ T细胞的CD4+ T细胞重建的重组激活基因2缺陷小鼠以及缺乏CD1d限制性NKT细胞的CD1-/-小鼠所产生的数据表明,这两种调节性CD4+ T亚群对FMN存活均无关键作用。