Katsuta H, Ashikawa K, Takaoka T
Jpn J Exp Med. 1975 Jun;45(3):223-9.
MM2 cells, ascitic tumor originated from spontaneous mammary carcinoma of C3H/He mouse, were mix-cultured with lymphoid cells of thymus or mesenteric lymph nodes from isologous animals of the same sex. The interaction in culture between these cells was examined by time-lapse cinemicrography. In single culture, thymocytes, mesenteric lymph node lymphocytes and MM2 cells were kept for 7 days with little change in cell population. Lymphocytes of both sources showed a marked decrease in cell number when cultured together with MM2 cells, being evidently phagocytosed by MM2 cells. Lymphocytes from MM2-bearing mice or mice sensitized with deoxycholate-extracted MM2 antigen were also all phagocytosed. MM2 cells exhibited no sign of damage or degeneration due to the phagocytosis. Thymocytes were not phagocytosed by histiocytes obtained from ascitic fluid 3 days after i.p. injection of 5% starch suspension. Phagocytosis of erythrocytes or lymphoid cells from spleen by MM2 cells was not detected.
MM2细胞是源自C3H/He小鼠自发性乳腺癌的腹水瘤细胞,将其与来自同性同系动物的胸腺或肠系膜淋巴结的淋巴细胞进行混合培养。通过延时显微电影摄影术检测这些细胞在培养中的相互作用。在单一培养中,胸腺细胞、肠系膜淋巴结淋巴细胞和MM2细胞培养7天,细胞数量变化不大。当与MM2细胞一起培养时,两种来源的淋巴细胞数量均显著减少,明显被MM2细胞吞噬。来自携带MM2肿瘤的小鼠或用脱氧胆酸盐提取的MM2抗原致敏的小鼠的淋巴细胞也全部被吞噬。MM2细胞未表现出因吞噬作用而受损或退化的迹象。腹腔注射5%淀粉悬液3天后,从腹水中获得的组织细胞未吞噬胸腺细胞。未检测到MM2细胞对红细胞或脾淋巴细胞的吞噬作用。