Fonteh A N, Chilton F H
Division of Pulmonary and Critical Care Medicine, Bowman Gray School of Medicine, Winston-Salem, NC 27157.
J Immunol. 1992 Mar 15;148(6):1784-91.
The objective of the present study was to better understand the remodeling of arachidonic acid (AA) in phospholipids of the mouse bone marrow-derived mast cell (BMMC) during Ag and ionophore A23187 activation. Initial studies were designed to understand the movement of AA in phospholipid classes under resting conditions. BMMC pulse labeled with AA incorporated greater than 95% of the label into the major phospholipid classes. Phosphatidylcholine (PC) subclasses, 1-acyl-2-arachidonoyl-(sn-glycero-3-phosphocholine (GPC)) in particular, initially accounted for most of the label incorporated into the cells with phosphatidylinositol/phosphatidylserine (PI/PS) and phosphatidylethanolamine (PE) subclasses containing much smaller quantities. Prolonged incubation of labeled BMMC resulted in a decrease in the radioactivity in PC with a concomitant increase in PE such that 1-alk-1-enyl-2-arachidonoyl-(sn-glycero-3-phosphoethanolamine (GPE)) became the single largest labeled AA pool by 24 h. Further experiments indicated that 24 h was the time required to reach isotopic equilibrium among AA-containing phospholipids of the BMMC. In the next series of experiments, BMMC phospholipids were labeled to different specific activities by either labeling the cells for 0.5 h or for 24 h followed by stimulation. Under isotopic equilibrium conditions (24 h), stimulation resulted in AA release from PE greater than PC much greater than PI/PS with 1-alk-1-enyl-2-arachidonoyl-GPE providing the bulk of AA released from the BMMC. By contrast, cells labeled for 0.5 h released AA from PC much greater than PI/PS, with 1-acyl-2-arachidonoyl-GPC accounting for most of the AA released from BMMC phospholipids. Label associated with PE subclasses under nonequilibrium conditions remained unchanged or slightly increased throughout a 10-min stimulation period. Finally, BMMC were double labeled with [14C]-AA for 24 h and then with [3H]-AA for 0.5 h. Cell stimulation resulted in a decrease in the [3H]/[14C] ratio in PC and PI and an increase in the ratio in PE. The decrease in [3H]/[14C] ratio in PC was mainly in 1-acyl-2-arachidonoyl-GPC, whereas the increase in PE subclasses was primarily in 1-alk-1-enyl-2-arachidonoyl-GPE. The [3H]/[14C] ratio in cellular neutral lipids and in supernatant fluid products were at values between PC and PE subclasses. Taken together, these data suggest that during Ag activation, the release of free arachidonic acid is from predominantly PE subclasses. Concomitant with the release of AA, there is a rapid remodeling of AA from PC subclasses into PE subclasses (1-alk-1-enyl-2-acyl-GPE).
本研究的目的是更好地了解在抗原和离子载体A23187激活过程中小鼠骨髓来源肥大细胞(BMMC)磷脂中花生四烯酸(AA)的重塑情况。最初的研究旨在了解静息条件下AA在磷脂类别中的移动情况。用AA脉冲标记的BMMC将超过95%的标记物掺入主要磷脂类别中。磷脂酰胆碱(PC)亚类,特别是1-酰基-2-花生四烯酰基-(sn-甘油-3-磷酸胆碱(GPC)),最初占掺入细胞的大部分标记物,而磷脂酰肌醇/磷脂酰丝氨酸(PI/PS)和磷脂酰乙醇胺(PE)亚类含有的量要少得多。标记的BMMC长时间孵育导致PC中的放射性降低,同时PE增加,以至于到24小时时,1-烯基-2-花生四烯酰基-(sn-甘油-3-磷酸乙醇胺(GPE))成为单个最大的标记AA池。进一步的实验表明,24小时是BMMC含AA磷脂达到同位素平衡所需的时间。在接下来的一系列实验中,通过将细胞标记0.5小时或24小时然后进行刺激,使BMMC磷脂标记到不同的比活度。在同位素平衡条件下(24小时),刺激导致AA从PE释放的量大于PC,远大于PI/PS,1-烯基-2-花生四烯酰基-GPE提供了从BMMC释放的大部分AA。相比之下,标记0.5小时的细胞从PC释放的AA远大于PI/PS,1-酰基-2-花生四烯酰基-GPC占从BMMC磷脂释放的大部分AA。在非平衡条件下与PE亚类相关的标记在整个10分钟刺激期内保持不变或略有增加。最后,BMMC先用[14C]-AA双标记24小时,然后用[3H]-AA标记0.5小时。细胞刺激导致PC和PI中的[3H]/[14C]比值降低,而PE中的比值增加。PC中[3H]/[14C]比值的降低主要发生在1-酰基-2-花生四烯酰基-GPC中,而PE亚类中的增加主要发生在1-烯基-2-花生四烯酰基-GPE中。细胞中性脂质和上清液产物中的[3H]/[14C]比值介于PC和PE亚类之间。综上所述,这些数据表明在抗原激活过程中,游离花生四烯酸的释放主要来自PE亚类。伴随着AA的释放,AA从PC亚类快速重塑为PE亚类(1-烯基-2-酰基-GPE)。