Ruschmeyer D, Thude H, Mühlradt P F
Immunology Research Group, Gesellschaft für Biotechnologische Forschung, Braunschweig, FRG.
FEMS Immunol Med Microbiol. 1993 Oct;7(3):223-9. doi: 10.1111/j.1574-695X.1993.tb00402.x.
In continuation of previous work on macrophage activation by a Mycoplasma fermentans-derived product, originally named "mycoplasma-derived high mol. wt. material" (MDHM), we have investigated whether MDHM was capable of inducing synthesis of the reactive nitrogen intermediate nitric oxide (NO), thus rendering macrophages cytocidal. Mycoplasmas were first delipidated with acetone, and MDHM activity was then extracted with 50 mM 1-O-octyl-beta-D-glucopyranoside to yield a particularly active new preparation of MDHM which we have named MDHM-D (D for detergent). In combination with IFN-gamma, MDHM-D activated macrophages to produce reactive nitrogen intermediates and kill P815 mastocytoma cells in co-culture. P815 target cells were chosen because they are TNF-resistant. Macrophages from the LPS-low responder strain C3H/HeJ were used to minimize interference from possible LPS contamination. MDHM-D activity in this system was strictly IFN-gamma-dependent. In the presence of 25 U/ml IFN-gamma MDHM-D gave a half maximal response at a dilution of 1/100,000, showing a parallel concentration dependency for nitrite production and cytocidal activity.
在先前关于发酵支原体衍生产品激活巨噬细胞的工作基础上继续开展研究,该产品最初命名为“支原体衍生高分子量物质”(MDHM),我们研究了MDHM是否能够诱导活性氮中间体一氧化氮(NO)的合成,从而使巨噬细胞具有杀细胞作用。支原体先用丙酮脱脂,然后用50 mM 1-O-辛基-β-D-吡喃葡萄糖苷提取MDHM活性,得到一种特别活跃的MDHM新制剂,我们将其命名为MDHM-D(D代表去污剂)。与IFN-γ联合使用时,MDHM-D可激活巨噬细胞产生活性氮中间体,并在共培养中杀死P815肥大细胞瘤细胞。选择P815靶细胞是因为它们对TNF有抗性。使用来自LPS低反应性品系C3H/HeJ的巨噬细胞,以尽量减少可能的LPS污染带来的干扰。该系统中MDHM-D的活性严格依赖于IFN-γ。在存在25 U/ml IFN-γ的情况下,MDHM-D在1/100,000的稀释度下产生半数最大反应,表明亚硝酸盐产生和杀细胞活性具有平行的浓度依赖性。