Vitetta E S, Uhr J W
J Immunol. 1975 Aug;115(2):374-81.
The synthesis and turnover of cell surface H-2 alloantigens were studied in murine splenocytes by the anti-H-2-bind method to separate precursor-labeled surface from intracellular molecules. Results indicate that newly synthesized H-2 antigen, labeled in either its peptide or carbohydrate portion enters a relatively small pool of intracellular H-2 antigen and then is rapidly transported to the plasma membrane which represents a larger compartment. The simplest interpretation of these findings is that H-2 antigen is synthesized and transported along a conventional secretory pathway. Pulse-chase experiments indicate that H-2 antigens are not readily chased from the plasma membrane and are not shed or internalized during short-term culture. The aforementioned observations are discussed in terms of a cellular heterogeneity.
采用抗H-2结合法研究了小鼠脾细胞中细胞表面H-2同种抗原的合成与周转,以将前体标记的表面分子与细胞内分子分离。结果表明,新合成的H-2抗原,无论是其肽段还是糖部分被标记,都会进入一个相对较小的细胞内H-2抗原池,然后迅速转运到代表更大区室的质膜。这些发现最简单的解释是,H-2抗原是沿着传统分泌途径合成和转运的。脉冲追踪实验表明,H-2抗原不易从质膜上被追踪,并且在短期培养过程中不会脱落或内化。上述观察结果将根据细胞异质性进行讨论。