Department of Neurology, Section of Developmental Neurobiology, University of Wuerzburg, Josef-Schneider Str. 11, D-97080 Wuerzburg, Germany.
Am J Pathol. 2010 Feb;176(2):549-55. doi: 10.2353/ajpath.2010.090722. Epub 2009 Dec 30.
In transgenic mice overexpressing the major myelin protein of the central nervous system, proteolipid protein, CD8+ T-lymphocytes mediate the primarily genetically caused myelin and axon damage. In the present study, we investigated the cellular and molecular mechanisms underlying this immune-related neural injury. At first, we investigated whether T-cell receptors (TCRs) are involved in these processes. For this purpose, we transferred bone marrow from mutants carrying TCRs with an ectopic specificity to ovalbumin into myelin mutant mice that also lacked normal intrinsic T-cells. T-lymphocytes with ovalbumin-specific TCRs entered the mutant central nervous system to a similar extent as T-lymphocytes from wild-type mice. However, as revealed by histology, electron microscopy and axon- and myelin-related immunocytochemistry, these T-cells did not cause neural damage in the myelin mutants, reflecting the need for specific antigen recognition by cytotoxic CD8+ T-cells. By chimerization with bone marrow from perforin- or granzyme B (Gzmb)-deficient mice, we demonstrated that absence of these cytotoxic molecules resulted in reduced neural damage in myelin mutant mice. Our study strongly suggests that pathogenetically relevant immune reactions in proteolipid protein-overexpressing mice are TCR-dependent and mediated by the classical components of CD8+ T-cell cytotoxicity, perforin, and Gzmb. These findings have high relevance with regard to our understanding of the pathogenesis of disorders primarily caused by genetically mediated oligodendropathy.
在过表达中枢神经系统主要髓鞘蛋白(即蛋白脂质蛋白)的转基因小鼠中,CD8+T 淋巴细胞介导了主要由遗传原因引起的髓鞘和轴突损伤。在本研究中,我们研究了这种免疫相关的神经损伤的细胞和分子机制。首先,我们研究了 T 细胞受体(TCRs)是否参与了这些过程。为此,我们将携带异常特异性 TCR 的骨髓从突变体转移到缺乏正常内在 T 细胞的髓鞘突变体小鼠中。具有卵清蛋白特异性 TCR 的 T 淋巴细胞进入突变体中枢神经系统的程度与野生型小鼠的 T 淋巴细胞相似。然而,正如组织学、电子显微镜和轴突和髓鞘相关免疫细胞化学所揭示的那样,这些 T 细胞在髓鞘突变体中没有引起神经损伤,这反映了细胞毒性 CD8+T 细胞需要特异性抗原识别。通过与穿孔素或颗粒酶 B(Gzmb)缺陷型小鼠的嵌合,我们证明了这些细胞毒性分子的缺失导致髓鞘突变体小鼠的神经损伤减少。我们的研究强烈表明,在过表达蛋白脂质蛋白的小鼠中,与病原体相关的免疫反应是 TCR 依赖性的,并由 CD8+T 细胞细胞毒性的经典成分、穿孔素和 Gzmb 介导。这些发现对于我们理解主要由遗传介导的少突胶质细胞病变引起的疾病的发病机制具有重要意义。