Nolfo R, Rankin J A
Department of Medicine, West Haven Veterans Administration Hospital, Connecticut.
Prostaglandins. 1990 Feb;39(2):157-65. doi: 10.1016/0090-6980(90)90072-4.
U937 and THP-1 cells possess some characteristics of human mononuclear phagocytes, cells which synthesize and release LTB4, LTC4, and LTD4. Incubation of these cells with recombinant human interferon-gamma (IFN-gamma) or Phorbol Myristate Acetate (PMA) induces a more differentiated cell state. We hypothesized that U937 and THP-1 cells would release LTB4, LTC4, and LTD4 in response to stimulation with the non-physiologic agonist, calcium ionophore A23187 and that preincubation with IFN-gamma or PMA might alter leukotriene release by these cells. We cultured both cell lines for 48 hours in the presence and absence of IFN-gamma (1000 units/ml) and for 120 hours in the presence and absence of PMA (160 nM) and then challenged them with A23187 (5uM) for 30 minutes at 37 degrees C. The supernatants were deproteinated and assayed by RIA for LTB4 and LTC4 and by RP-HPLC for LTB4, LTC4, and LTD4. Neither U937 nor THP-1 cells released quantities of leukotrienes detectable by RIA, less than 0.3ng/5 X 10(6) cells. Peripheral blood mononuclear phagocytes from normal volunteers, cultured and challenged in vitro at under identical conditions, released 11.3 +/- 2.9 ng LTB4 and 2.0 +/- 1.5 ng LTC4/10(6) viable monocytes. The lack of leukotriene production by U937 and THP-1 cells was not altered by preincubation for 48 hours with IFN-gamma (n = 3) nor by preincubation with PMA for 120 hours (n = 3). We conclude 1) U937 and THP-1 cells do not appear to be appropriate in vitro models for the examination of leukotriene release from normal mononuclear phagocytes. 2) Pre-incubation of U937 and THP-1 cells with IFN-gamma or PMA under the conditions tested, does not induce the ability of these cell lines to release leukotrienes.
U937和THP-1细胞具有人类单核吞噬细胞的一些特性,这类细胞能合成并释放白三烯B4(LTB4)、白三烯C4(LTC4)和白三烯D4(LTD4)。用重组人干扰素-γ(IFN-γ)或佛波酯(PMA)孵育这些细胞会诱导其进入更分化的细胞状态。我们推测,U937和THP-1细胞会在非生理性激动剂钙离子载体A23187的刺激下释放LTB4、LTC4和LTD4,并且用IFN-γ或PMA预孵育可能会改变这些细胞的白三烯释放情况。我们在有和没有IFN-γ(1000单位/毫升)的情况下将两种细胞系培养48小时,在有和没有PMA(160纳摩尔)的情况下培养120小时,然后在37℃用A23187(5微摩尔)刺激它们30分钟。将上清液进行脱蛋白处理,并用放射免疫分析法(RIA)检测LTB4和LTC4,用反相高效液相色谱法(RP-HPLC)检测LTB4、LTC4和LTD4。U937和THP-1细胞释放的白三烯量均无法通过RIA检测到,每5×10⁶个细胞释放量少于0.3纳克。来自正常志愿者的外周血单核吞噬细胞在相同条件下进行体外培养和刺激,每10⁶个存活单核细胞释放11.3±2.9纳克LTB4和2.0±1.5纳克LTC4。U937和THP-1细胞缺乏白三烯生成的情况,在与IFN-γ预孵育48小时(n = 3)或与PMA预孵育120小时(n = 3)后均未改变。我们得出结论:1)U937和THP-1细胞似乎不是用于研究正常单核吞噬细胞释放白三烯的合适体外模型。2)在测试条件下,用IFN-γ或PMA对U937和THP-1细胞进行预孵育,不会诱导这些细胞系释放白三烯的能力。