Swain S, Modabber F, Coons A H
J Immunol. 1976 Apr;116(4):915-22.
The results reported in this paper demonstrate that the enumeration of cells binding beta-galactosidase (Z) as an antigen, revealed by subsequent substrate hydrolysis, is an excellent method for the detection and study of antigen-binding cells (ZBC). The binding found is specific and is restricted to a small number of lymphocytes that bind a large number of Z molecules via surface receptors. Such ZBC were found at mean frequencies of 150 per 10(6) in the thymus and 200 to 300 per 10(6) in the spleen. The binding cells of both organs were heterogenous with individual ZBC binding from 10(5) to 10(6) molecules of enzyme as determined by substrate hydrolysis, although this might well be an overestimate of the number of actual receptors. The profiles for the frequency of ZBC binding different numbers of molecules were nearly identical for thymus and spleen, in contrast to descriptions of the binding of many other antigens. Receptors responsible for Z binding appear to be superficially located on the cell since they are trypsin-sensitive to a large extent and are not increased by fixation.
本文报道的结果表明,通过随后的底物水解来计数结合β-半乳糖苷酶(Z)作为抗原的细胞,是检测和研究抗原结合细胞(ZBC)的一种极佳方法。所发现的结合是特异性的,并且仅限于通过表面受体结合大量Z分子的少数淋巴细胞。在胸腺中,此类ZBC的平均频率为每10^6个细胞中有150个,在脾脏中为每10^6个细胞中有200至300个。通过底物水解测定,两个器官中的结合细胞都是异质性的,单个ZBC结合10^5至10^6个酶分子,尽管这很可能高估了实际受体的数量。与许多其他抗原结合的描述相反,胸腺和脾脏中结合不同数量分子的ZBC频率分布几乎相同。负责Z结合的受体似乎位于细胞表面,因为它们在很大程度上对胰蛋白酶敏感,并且不会因固定而增加。