Kondomerkos Dimitrios J, Kalamidas Stefanos A, Michalis Lampros K, Kanavaros Panagiotis
Department of Anatomy, Histology and Embryology, Medical School, University of Ioannina, 45110 Ioannina, Greece.
In Vivo. 2004 Sep-Oct;18(5):653-9.
Macrophages that uptake modified lipoproteins are activated and may initially behave as endotoxin-stimulated macrophages. This study was undertaken in order to determine whether signal transduction pathways controlling endotoxin-mediated activation may also influence the lipoprotein-mediated activation of macrophages.
Rat peritoneal macrophages were incubated for 16 hours with acetylated low-density lipoprotein and certain agents that modify the phosphoinositide/calcium- and cyclic AMP-mediated pathways, such as 2-[4-morpholinyl]-8-phenyl-1[4H]-benzopyran-4-one (LY-294002), autocamtide 2-related inhibitory peptide (AIP), N-(2-[p-bromocinnamylamino]-ethyl)-5-isoquinolinesulfonamide hydrochloride (H-89) and actinomycin D. The production of nitric oxide and the intracellular and extracellular activities of acid phosphatase were assayed.
Macrophages incubated with acetylated low-density lipoprotein showed an increased production of nitric oxide and intracellular acid phosphatase activity as compared to their controls. LY-294002, AIP and H-89 caused a significant decrease in nitric oxide production and intracellular acid phosphatase activity. Actinomycin D had similar effects. AIP and actinomycin also significantly increased extracellular acid phosphatase activity.
The activation of peritoneal macrophages by acetylated low-density lipoprotein was similar to the activation by endotoxin, as expressed by the nitric oxide production and acid phosphatase intracellular activity; agents controlling the phosphoinositide/calcium- and cyclic AMP-mediated pathways in endotoxin-activated macrophages also influence the acetylated low-density lipoprotein-activated macrophages.
摄取修饰脂蛋白的巨噬细胞被激活,最初可能表现为内毒素刺激的巨噬细胞。进行本研究以确定控制内毒素介导激活的信号转导途径是否也会影响脂蛋白介导的巨噬细胞激活。
将大鼠腹腔巨噬细胞与乙酰化低密度脂蛋白及某些修饰磷酸肌醇/钙和环磷酸腺苷介导途径的试剂一起孵育16小时,这些试剂如2-[4-吗啉基]-8-苯基-1[4H]-苯并吡喃-4-酮(LY-294002)、自抑制肽2相关抑制肽(AIP)、N-(2-[对溴肉桂氨基]乙基)-5-异喹啉磺酰胺盐酸盐(H-89)和放线菌素D。检测一氧化氮的产生以及酸性磷酸酶的细胞内和细胞外活性。
与对照组相比,用乙酰化低密度脂蛋白孵育的巨噬细胞一氧化氮产生增加,细胞内酸性磷酸酶活性增强。LY-294002、AIP和H-89使一氧化氮产生和细胞内酸性磷酸酶活性显著降低。放线菌素D有类似作用。AIP和放线菌素也显著增加细胞外酸性磷酸酶活性。
乙酰化低密度脂蛋白对腹腔巨噬细胞的激活与内毒素激活相似,以一氧化氮产生和酸性磷酸酶细胞内活性表示;在内毒素激活的巨噬细胞中控制磷酸肌醇/钙和环磷酸腺苷介导途径的试剂也会影响乙酰化低密度脂蛋白激活的巨噬细胞。