Quinn M T, Kondratenko N, Parthasarathy S
Department of Medicine, University of California, San Diego, La Jolla 92093-0613.
Biochim Biophys Acta. 1991 Apr 3;1082(3):293-302. doi: 10.1016/0005-2760(91)90205-v.
Previously, we reported that lysophosphatidylcholine (lyso-PtdCho), a component of oxidized low-density lipoprotein, was a monocyte chemoattractant (M.T. Quinn et al. (1988) Proc. Natl. Acad. Sci. USA 85, 2805-2809). Monocyte chemotaxis was also stimulated by lyso-platelet activating factor but not by platelet activating factor itself. In the present studies, we used other analogs of lyso-PtdCho to determine structural and metabolic features required for chemotactic activity. Although both D- and L-lyso-PtdCho stimulated chemotaxis, suggesting a lack of stereospecificity, studies using propanediol and ethanediol analogs of lyso-PtdCho suggested that a free hydroxyl moiety or an ester-linked fatty acid vicinal to the phosphocholine group of the lysophospholipid was required for the expression of activity. Incubation of [3H]choline-labeled lyso-PtdCho with monocytes resulted in the formation of labeled PtdCho, glycerophosphocholine (GPC), phosphocholine, and free choline, while resident peritoneal macrophages, cells which we show do not respond chemotactically to lyso-PtdCho, metabolized the labeled substrate to generate only labeled PtdCho and GPC; no labeled phosphocholine was found, suggesting a possible role for lysophospholipase C activity in the monocyte chemotactic response. Although monoacylglycerol, the product of lysophospholipase C hydrolysis of lyso-PtdCho, was not chemotactic for monocytes, diacylglycerol demonstrated chemotactic activity, suggesting that the subsequent acylation to diacylglycerol may be involved in the monocyte chemotactic response to lyso-PtdCho. Indeed, monocytes incorporated [3H]glycerol from [3H]glycerol-labeled lyso-PtdCho into di- and triacylglycerol. Based on these results, a model is proposed whereby the monocyte chemotactic response to lyso-PtdCho involves a sequence of metabolic steps which includes hydrolysis of lyso-PtdCho to monoacylglycerol and phosphocholine by lysophospholipase C followed by acylation of monoacylglycerol to diacylglycerol. Diacylglycerol would then act as an intracellular second messenger that could activate or facilitate the chemotactic response.
此前,我们报道过氧化型低密度脂蛋白的一种成分溶血磷脂酰胆碱(lyso - PtdCho)是一种单核细胞趋化剂(M.T. 奎因等人(1988年)《美国国家科学院院刊》85卷,2805 - 2809页)。溶血血小板活化因子也能刺激单核细胞趋化,但血小板活化因子本身却不能。在本研究中,我们使用溶血磷脂酰胆碱的其他类似物来确定趋化活性所需的结构和代谢特征。尽管D型和L型溶血磷脂酰胆碱都能刺激趋化,这表明缺乏立体特异性,但使用溶血磷脂酰胆碱的丙二醇和乙二醇类似物的研究表明,溶血磷脂的磷酸胆碱基团附近的游离羟基部分或酯连接的脂肪酸对于活性表达是必需的。用[³H]胆碱标记的溶血磷脂酰胆碱与单核细胞一起孵育会导致标记的磷脂酰胆碱(PtdCho)、甘油磷酸胆碱(GPC)、磷酸胆碱和游离胆碱的形成,而我们发现驻留腹膜巨噬细胞对溶血磷脂酰胆碱没有趋化反应,它们将标记的底物代谢仅生成标记的磷脂酰胆碱和甘油磷酸胆碱;未发现标记的磷酸胆碱,这表明溶血磷脂酶C活性在单核细胞趋化反应中可能起作用。尽管溶血磷脂酰胆碱经溶血磷脂酶C水解产生的单酰甘油对单核细胞没有趋化作用,但二酰甘油表现出趋化活性,这表明随后向二酰甘油的酰化可能参与单核细胞对溶血磷脂酰胆碱的趋化反应。实际上,单核细胞将[³H]甘油标记的溶血磷脂酰胆碱中的[³H]甘油掺入二酰甘油和三酰甘油中。基于这些结果,提出了一个模型,据此单核细胞对溶血磷脂酰胆碱的趋化反应涉及一系列代谢步骤,包括溶血磷脂酶C将溶血磷脂酰胆碱水解为单酰甘油和磷酸胆碱,随后单酰甘油酰化为二酰甘油。然后二酰甘油将作为一种细胞内第二信使,可激活或促进趋化反应。