Tanigawa T, Takayama H, Osatake H, Tanaka K, Kasagi N, Tanaka Y
Department of Bacteriology, Faculty of Medicine, Tottori University, Yonago, Japan.
Cytotechnology. 1992;10(1):43-51. doi: 10.1007/BF00376099.
Characteristics of mouse macrophage (MP) cell lines A640-BB-2, J774.1 and P388D1 and mouse peritoneal exudate MPs were studied and compared in cell morphology, ability to recognize tumor cells in the presence and absence of OK-432 known to activate MPs, and in lysosomal enzyme activity. In A640-BB-2 cells and exudate MPs, cell surfaces showed a few ridge-like processes and microvilli; spontaneous cytotoxicity was moderate against tumor target L929, and little or absent against targets SV3T3, B-16 and U937; and lysosomal enzyme activity of nonspecific esterase, acid phosphatase, and beta-glucuronidase was high. After culture in the presence of OK-432, A640-BB-2 cells and exudate MPs showed more extensive spreading with larger surface areas and with increased numbers of ridge-like processes and microvilli, and their cytotoxicity against target L929 became more extensive. The stable soluble factor did not participate in the mechanism of cytotoxicity against target L929 mediated by A640-BB-2 cells and exudate MPs. J774.1 and P388D1 cells were different from exudate MPs in cell morphology and ability to recognize tumor cells when cultured either with or without OK-432, and in lysosomal enzyme activity. A640-BB-2 cells seem to be useful in studying MP-tumor cell interaction and MP activation, and in detecting the trace biological activating factor of MPs.
对小鼠巨噬细胞(MP)细胞系A640 - BB - 2、J774.1和P388D1以及小鼠腹腔渗出液巨噬细胞的特性进行了研究,并在细胞形态、在存在和不存在已知可激活巨噬细胞的OK - 432的情况下识别肿瘤细胞的能力以及溶酶体酶活性方面进行了比较。在A640 - BB - 2细胞和渗出液巨噬细胞中,细胞表面显示出一些脊状突起和微绒毛;对肿瘤靶细胞L929的自发细胞毒性中等,对靶细胞SV3T3、B - 16和U937的细胞毒性很小或不存在;非特异性酯酶、酸性磷酸酶和β - 葡萄糖醛酸酶的溶酶体酶活性较高。在OK - 432存在下培养后,A640 - BB - 2细胞和渗出液巨噬细胞显示出更广泛的铺展,表面积更大,脊状突起和微绒毛数量增加,并且它们对靶细胞L929的细胞毒性变得更广泛。稳定的可溶性因子不参与A640 - BB - 2细胞和渗出液巨噬细胞介导的对靶细胞L929的细胞毒性机制。J774.1和P388D1细胞在细胞形态、在有或没有OK - 432培养时识别肿瘤细胞的能力以及溶酶体酶活性方面与渗出液巨噬细胞不同。A640 - BB - 2细胞似乎有助于研究巨噬细胞 - 肿瘤细胞相互作用和巨噬细胞激活,以及检测巨噬细胞的微量生物激活因子。