Scott W A, Zrike J M, Hamill A L, Kempe J, Cohn Z A
J Exp Med. 1980 Aug 1;152(2):324-35. doi: 10.1084/jem.152.2.324.
The lipids of mouse peritoneal macrophages contain high levels (25 mole percent) of esterified arachidonic acid (20:4). Following in vitro exposure to unopsonized zymosan, these cells synthesize and release oxygenated products of 20:4. Maximal levels of zymosan ingestion promote the release of 40-50% of the 20:4 content of cultures without loss of viabilitiy. Release of radiolabel from macrophages prelabeled with [3H]20:4 provides a quantitative measure for the synthesis of 20:4-derived products. Approximately 67% of the released 20:4 is recovered as prostaglandins (PG) (51% PGE and 16% 6-oxo-PGF1 alpha) and the remainder as apolar products tentatively identified as hydroxy-eicosatetraenoic acids. The kinetics of synthesis are comparable for both sets of products. A detailed examination of PGE synthesis indicated the PGE levels rise in parallel with phagocytosis during a continuous exposure of macrophages to zymosan. The concentration of particles determines the initial rate of PGE release, but the time-course of synthesis is finite (approximately 60 min), regardless of the zymosan dose. These observations are compatible with the notion that phagocytosis results in a burst of PG synthesis, the size of which is determined by the phagocytic stimulus. This is supported by the finding that secondary challenges of zymosan promote new rounds of PG synthesis by macrophages.
小鼠腹腔巨噬细胞的脂质含有高水平(25摩尔百分比)的酯化花生四烯酸(20:4)。在体外暴露于未调理的酵母聚糖后,这些细胞合成并释放20:4的氧化产物。酵母聚糖摄取的最大水平促进了培养物中20:4含量的40 - 50%的释放,而不会丧失活力。用[3H]20:4预标记的巨噬细胞释放放射性标记物为20:4衍生产物的合成提供了一种定量测量方法。释放的20:4中约67%以前列腺素(PG)形式回收(51%为PGE,16%为6-氧代-PGF1α),其余为暂定为羟基二十碳四烯酸的非极性产物。两组产物的合成动力学相当。对PGE合成的详细检查表明,在巨噬细胞持续暴露于酵母聚糖期间,PGE水平与吞噬作用平行升高。颗粒浓度决定了PGE释放的初始速率,但合成的时间进程是有限的(约60分钟),与酵母聚糖剂量无关。这些观察结果与吞噬作用导致PG合成爆发的观点一致,其大小由吞噬刺激决定。酵母聚糖的二次刺激促进巨噬细胞新一轮PG合成的发现支持了这一点。