Molnár Eszter, Prechl József, Erdei Anna
Department of Immunology, Loránd Eötvös University, Pázmány Péter s. 1/C, 1117 Budapest, Hungary.
Immunol Lett. 2008 Mar 15;116(2):163-7. doi: 10.1016/j.imlet.2007.12.010. Epub 2008 Jan 18.
In mice CR1 and CR2 are encoded at a single locus and the two alternatively spliced RNA transcripts of the CD21 gene generate murine CR1 and CR2 (CR1/2). While the function of CD21 has been extensively studied on murine B lymphocytes, much less is known about its appearance and role on T cells. Earlier we had demonstrated the expression of CR1/2 on activated murine T cells by cytofluorymetry and immunoprecipitation and proposed its role in the enhancement of antigen presentation by B cells and macrophages bearing C3-fragments. In this study we analyze the expression-profile and further possible roles of CR1/2 on T lymphocytes. We describe a CR1/2 expressing CD4+ T cell subpopulation present in the mesenteric lymph nodes of mice. We show that these cells can be activated by the CD21-specific 7G6 single chain antibody, and demonstrate that activation via this complement receptor results in the translocation of NF-kappaB to the nucleus. Interestingly we found a substantial elevation of CD21+ T cells during both spontaneous and ceramide-induced apoptosis.
在小鼠中,CR1和CR2由单个基因座编码,CD21基因的两种可变剪接RNA转录本产生小鼠CR1和CR2(CR1/2)。虽然CD21的功能已在小鼠B淋巴细胞上得到广泛研究,但对其在T细胞上的出现和作用了解较少。此前我们通过细胞荧光分析和免疫沉淀证明了CR1/2在活化的小鼠T细胞上的表达,并提出其在增强携带C3片段的B细胞和巨噬细胞的抗原呈递中的作用。在本研究中,我们分析了CR1/2在T淋巴细胞上的表达谱及其进一步可能的作用。我们描述了存在于小鼠肠系膜淋巴结中的表达CR1/2的CD4+ T细胞亚群。我们表明这些细胞可被CD21特异性7G6单链抗体激活,并证明通过这种补体受体的激活导致NF-κB易位至细胞核。有趣的是,我们发现在自发凋亡和神经酰胺诱导的凋亡过程中,CD21+ T细胞均有显著增加。