Forni L, Coutinho A
Eur J Immunol. 1978 Jan;8(1):56-62. doi: 10.1002/eji.1830080112.
Rabbit antisera have been prepared against spleen B cells from C3H/Tif mice, high responders to lipopolysaccharide (LPS). After complete absorption on tissues of C3H/Hej mice (LPS nonresponders), such antisera specifically stain and kill (in the presence of complement) a fraction of the B cells from a number of LPS high responder strains, and fail to recognize any cells in two different LPS nonresponder strains, C3H/HeJ and C57B1/10.Sc.Cr. The ontogeny, organ and strain distribution of this B cell marker parallels LPS reactivity. Frequencies of cells stained by this antiserum correspond to the frequencies of LPS-reactive B cell precursors recently determined. This antigent(s) is expressed by LPS-activated B cell blasts but not by cells which remain small after 48 h in the presence of LPS. Removal of the cells recognized by the antisera leads to depletion of LPS-reactive cells, while enriching for reactivity to another B cell mitogen, e.g. lipoprotein.
已制备出针对C3H/Tif小鼠脾脏B细胞的兔抗血清,C3H/Tif小鼠对脂多糖(LPS)反应强烈。在C3H/Hej小鼠(LPS无反应者)的组织上完全吸收后,这种抗血清能特异性地染色并(在补体存在的情况下)杀死来自多种LPS高反应性品系的一部分B细胞,并且无法识别两种不同的LPS无反应性品系C3H/HeJ和C57B1/10.Sc.Cr中的任何细胞。这种B细胞标志物的个体发生、器官和品系分布与LPS反应性相似。被这种抗血清染色的细胞频率与最近确定的LPS反应性B细胞前体频率相对应。这种抗原由LPS激活的B细胞母细胞表达,但不由在LPS存在下48小时后仍保持小细胞状态的细胞表达。去除被抗血清识别的细胞会导致LPS反应性细胞的耗竭,同时增强对另一种B细胞有丝分裂原(如脂蛋白)的反应性。