Novogrodsky A
J Immunol. 1975 Mar;114(3):1089-93.
Treatment of mouse spleen cells with periodate (NaIO4) or with neuraminidase and galactose oxidase (NAGO) induces blastogenesis and renders the cells cytotoxic to mastocytoma (P815) target cells. Treatment of target cells (P815 cells and turkey erythrocytes) with NaIO4 or with NAGO renders them susceptible to cytolysis by untreated mouse spleen cells. The cytotoxicity induced by NaIO4 is reduced upon reacting the NaIO4-treated, effector or target cells with borohydride or hydroxylamine. Thus the formation of free surface aldehydes on either the effector or target cell induced a cytotoxic effect. It is postulated that cross-linkage via a Schiff base between effector and target cell initiates the cytotoxic effect. Cytotoxicity induced by NaIO4 or NAGO is immunologically nonspecific and is independent of major antigenic differences between effector and target cells. Phagocytic cells are not involved in NaIO4-or NAGO-induced cytotoxicity toward P815 target cells.
用高碘酸盐(NaIO4)或神经氨酸酶和半乳糖氧化酶(NAGO)处理小鼠脾细胞可诱导细胞增殖,并使细胞对肥大细胞瘤(P815)靶细胞产生细胞毒性。用NaIO4或NAGO处理靶细胞(P815细胞和火鸡红细胞)会使它们易被未处理的小鼠脾细胞溶解。在用硼氢化钠或羟胺处理经NaIO4处理的效应细胞或靶细胞后,NaIO4诱导的细胞毒性会降低。因此,效应细胞或靶细胞上自由表面醛的形成会诱导细胞毒性作用。据推测,效应细胞和靶细胞之间通过席夫碱的交联引发了细胞毒性作用。NaIO4或NAGO诱导的细胞毒性在免疫上是非特异性的,并且与效应细胞和靶细胞之间的主要抗原差异无关。吞噬细胞不参与NaIO4或NAGO诱导的对P815靶细胞的细胞毒性作用。