Emerson S G, Cone R E
J Immunol. 1979 Mar;122(3):892-9.
Lactoperoxidase-catalyzed radioiodination was used to examine the metabolic fate of surface Ia antigens on murine spleen cells in culture. Ia antigens, detected predominately on splenic B lymphocytes, were lost from the cultured cells with biphasic kinetics: a 4 to 6 hr rapid phase, t 1/2 = 5 hr followed by slow release through 20 hr, t 1/2 = 30 hr. The rapid loss of Ia antigens observed was abolished by both harsh iodination conditions and nonphysiologic incubation conditions. The rapid decline in Ia activity was shown to be due to shedding of intact Ia antigens from the cell and to predominant release of IA subregion-coded proteins. Release of Ia antigens from the cell was accomplished by replacement at the cell surface, and thus reflected net membrane Ia turnover. Ia shedding was shown to be extremely temperature dependent, reflecting both a comparatively high activation enthalpy and entropy requirement for turnover.
乳过氧化物酶催化的放射性碘化用于检测培养的小鼠脾细胞表面Ia抗原的代谢命运。Ia抗原主要在脾脏B淋巴细胞上检测到,其在培养细胞中以双相动力学方式丢失:4至6小时的快速相,t1/2 = 5小时,随后在20小时内缓慢释放,t1/2 = 30小时。观察到的Ia抗原的快速丢失在苛刻的碘化条件和非生理孵育条件下均被消除。Ia活性的快速下降被证明是由于完整的Ia抗原从细胞上脱落以及IA亚区域编码蛋白的主要释放。Ia抗原从细胞中的释放是通过细胞表面的置换完成的,因此反映了细胞膜Ia的净周转。Ia脱落被证明极度依赖温度,反映了周转相对较高的活化焓和熵需求。