Hamilton T A, Fishman M
J Immunol. 1981 Oct;127(4):1702-6.
The interaction between tumoricidal rat peritoneal exudate macrophages and normal or neoplastic target cells has been examined both with respect to the sensitivity of the target cells to macrophage-mediated cytolysis and the ability of such targets to compete with one another for the lytic activity of macrophages. The results demonstrate that, in confirmation of earlier work from other laboratories, target cells are either sensitive or largely resistant to lysis, and such sensitivity correlates well with the neoplastic phenotype of the target cell. However, in target cell competition experiments all cultured cells as well as Con A-stimulated splenocytes and freshly isolated thymocytes exhibit the capacity to block cytolysis of sensitive indicator targets. In contrast, freshly prepared non-mitogen-stimulated splenic or lymph node lymphocytes are completely devoid of competitive activity. These results show that macrophages can recognize and interact with both normal and tumorigenic cells and that such target recognition can be distinguished from target cytolysis. Furthermore, the evidence suggests that at least 1 target cell feature that correlates with recognition is cell cycle traverse.
已针对肿瘤细胞杀伤性大鼠腹膜渗出巨噬细胞与正常或肿瘤靶细胞之间的相互作用,从靶细胞对巨噬细胞介导的细胞溶解的敏感性以及此类靶细胞相互竞争巨噬细胞裂解活性的能力两方面进行了研究。结果表明,正如其他实验室早期研究证实的那样,靶细胞对裂解要么敏感,要么基本具有抗性,且这种敏感性与靶细胞的肿瘤表型密切相关。然而,在靶细胞竞争实验中,所有培养细胞以及伴刀豆球蛋白A刺激的脾细胞和新鲜分离的胸腺细胞均表现出阻断敏感指示靶细胞细胞溶解的能力。相比之下,新鲜制备的未受丝裂原刺激的脾淋巴细胞或淋巴结淋巴细胞则完全没有竞争活性。这些结果表明,巨噬细胞能够识别正常细胞和致瘤细胞并与之相互作用,且这种靶细胞识别可与靶细胞溶解区分开来。此外,有证据表明,至少一种与识别相关的靶细胞特征是细胞周期进程。