Grant E P, Rock K L
Dana-Farber Cancer Institute, Division of Lymphocyte Biology, Boston, MA 02115.
J Immunol. 1992 Jan 1;148(1):13-8.
We have used a T-T hybridoma, RF33.70, to detect the MHC class I-restricted presentation of exogenous native OVA by thymic APC in vitro. Presentation of OVA with class I molecules by thymic APC requires intracellular processing. Phenotypic analyses indicated that low bouyant density, MHC class II+, FcR+ cells are capable of using this presentation pathway. In order to determine whether thymic APC have this function in vivo, thymic APC were isolated from mice after i.v. injection of native OVA. We find that OVA is presented in association with MHC class I, but not class II, molecules in the thymus. This is in contrast to splenic APC, which present exogenous OVA with both class I and class II molecules under these conditions. Our findings have implications for the repertoire of self-peptides that might be presented by thymic APC to developing T lymphocytes.
我们使用了一种T-T杂交瘤RF33.70,来检测胸腺抗原呈递细胞(APC)在体外对天然外源性卵清蛋白(OVA)的MHC I类限制性呈递。胸腺APC通过I类分子呈递OVA需要细胞内加工。表型分析表明,低浮力密度、MHC II类阳性、FcR阳性细胞能够利用这种呈递途径。为了确定胸腺APC在体内是否具有这种功能,在静脉注射天然OVA后从小鼠中分离出胸腺APC。我们发现,OVA在胸腺中与MHC I类分子而非II类分子结合呈递。这与脾APC形成对比,在这些条件下,脾APC会同时通过I类和II类分子呈递外源性OVA。我们的研究结果对胸腺APC可能呈递给发育中的T淋巴细胞的自身肽库具有启示意义。