Fritz R B, Zhao M L
Department of Microbiology, Medical College of Wisconsin, Milwaukee 53226, USA.
J Immunol. 1996 Dec 15;157(12):5249-53.
Previous studies have shown golli-myelin basic protein (MBP) mRNA to be expressed in the thymus of normal SJL mice, but translation of the mRNA was not assessed. To test for the presence of immunoreactive protein, single cell suspensions were prepared from adult SJL thymus and cultured with syngeneic MBP-specific T cells. After 48 h [3H]thymidine was added to the microcultures to assess T cell proliferation. MBP-specific T cell lines proliferated strongly (stimulation index range, 13-31). T cell lines specific for MBP exon 2, MBP peptide 89-101, proteolipid protein peptide 139-151, and OVA gave stimulation indices of 10-13, 5-6, 2-3, and 2-3, respectively. Stimulatory activity could be abrogated by irradiation of either the thymic cells or the MBP-specific T cells. Stimulatory activity was a property of a minor population of plastic-adherent thymic cells. Monoclonal anti-I-As Ab added to the microcultures inhibited the reaction by 77%. MBP-specific T cells cultured with syngeneic nonirradiated thymus cells in the absence of added MBP transferred experimental autoimmune encephalomyelitis adoptively to syngeneic recipients. These findings indicate that golli-MBP mRNA is translated in normal SJL thymus, and that peptides reactive with MBP-specific T cells in the context of class II MHC molecules are expressed.
以往研究表明,golli-髓鞘碱性蛋白(MBP)mRNA在正常SJL小鼠的胸腺中表达,但未评估该mRNA的翻译情况。为检测免疫反应性蛋白的存在,从成年SJL小鼠胸腺制备单细胞悬液,并与同基因MBP特异性T细胞共培养。48小时后,向微量培养物中加入[³H]胸腺嘧啶核苷以评估T细胞增殖。MBP特异性T细胞系强烈增殖(刺激指数范围为13 - 31)。针对MBP外显子2、MBP肽89 - 101、蛋白脂质蛋白肽139 - 151和OVA的T细胞系的刺激指数分别为10 - 13、5 - 6、2 - 3和2 - 3。胸腺细胞或MBP特异性T细胞的照射可消除刺激活性。刺激活性是少数塑料贴壁胸腺细胞群体的特性。添加到微量培养物中的单克隆抗I-Ab抗体可使反应抑制77%。在不添加MBP的情况下,将同基因未照射的胸腺细胞与MBP特异性T细胞共培养,可将实验性自身免疫性脑脊髓炎过继转移给同基因受体。这些发现表明,golli-MBP mRNA在正常SJL胸腺中被翻译,并且在II类MHC分子背景下与MBP特异性T细胞反应的肽被表达。