Natural killer cells do not mediate facial motoneuron survival after facial nerve transection

被引:22
作者
Byram, SC
Serpe, CJ
Pruett, SB
Sanders, VM
Jones, KJ
机构
[1] Loyola Univ, Med Ctr, Dept Cell Biol Neurobiol & Anat, Maywood, IL 60153 USA
[2] Edward Hines Jr VA Hosp, Res & Dev Serv, Hines, IL 60141 USA
[3] Louisiana State Univ, Dept Cellular Biol & Anat, Shreveport, LA 71130 USA
[4] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
关键词
natural killer cells; NK cells; neuro-immune interactions; neuroimmunology; facial nerve; FMN; innate immunity; reconstitution; neuronal survival; peripheral nerve injury;
D O I
10.1016/S0889-1591(03)00089-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The goal of the current study was to determine if natural killer (NK) cells mediate facial motoneuron (FMN) survival following injury. Wild-type (WT), perforin/recombinase activating gene-2 knockout (pfp/RAG-2 KO), and common gamma-chain (gammac)/RAG-2 KO mice received a right facial nerve axotomy. In WT mice, FMN survival was 86 +/- 1.0% relative to the contralateral control side. In contrast, pfp/RAG-2 and gammac/RAG-2 KO mice exhibited significant decreases in FMN survival (similar to20% and similar to30%, respectively), relative to WT. Reconstitution of pfplRAG-2 and gammac/RAG-2 KO mice with normal NK cells alone, failed to restore FMN survival levels to those of WT, but did restore functional lytic activity against YAG-1 cells. Reconstitution of pfp/RAG-2 and gammac/RAG-2 KO mice with splenocytes, and pfp/RAG-2 KO mice with CD4(+) T-lymphocytes alone or in combination with NK cells, restored FMN survival levels to those of WT. Thus, NK cells appear to not be a component of immune cell-mediated rescue of motoneurons from axotomy induced cell death. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:417 / 425
页数:9
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