Messner Maria C, Albert Carolyn J, Hsu Fong-Fu, Ford David A
Department of Biochemistry and Molecular Biology, St. Louis University Health Sciences Center, St. Louis, MO 63104, USA.
Chem Phys Lipids. 2006 Oct;144(1):34-44. doi: 10.1016/j.chemphyslip.2006.06.003. Epub 2006 Jul 3.
The plasmalogen sn-1 vinyl ether bond is targeted by hypochlorous acid (HOCl) produced by activated phagocytes. In the present study, the attack of the plasmalogen sn-1 vinyl ether bond by HOCl is shown to be preferred compared to the attack of double bonds present in the sn-2 position aliphatic chain (sn-2 alkenes) of both plasmenylcholine and phosphatidylcholine. Lysophosphatidylcholine (LPC) is a product from the initial HOCl attack of plasmenylcholine and the sn-2 alkene bonds present in this LPC product are secondary targets of HOCl leading to the production of LPC-chlorohydrins (ClOH). The aliphatic ClOH was demonstrated in both the positive and negative ion mode using collisionally-activated dissociation (CAD) of the molecular ion of LPC-ClOH. Furthermore, HOCl treatment of endothelial cells led to the preferential attack of plasmalogens in comparison to that of diacyl choline glycerophospholipids. Taken together, plasmenylcholine is oxidized preferentially over phosphatidylcholine and leads to the production of LPC-ClOH.
缩醛磷脂的sn-1乙烯基醚键会被活化吞噬细胞产生的次氯酸(HOCl)攻击。在本研究中,与HOCl对缩醛磷脂酰胆碱和磷脂酰胆碱的sn-2位脂肪链(sn-2烯烃)中双键的攻击相比,HOCl对缩醛磷脂sn-1乙烯基醚键的攻击更为优先。溶血磷脂酰胆碱(LPC)是HOCl最初攻击缩醛磷脂酰胆碱的产物,该LPC产物中存在的sn-2烯烃键是HOCl的次要攻击目标,会导致产生LPC-氯醇(ClOH)。利用LPC-ClOH分子离子的碰撞活化解离(CAD),在正离子和负离子模式下均证实了脂肪族ClOH的存在。此外,与二酰基胆碱甘油磷脂相比,HOCl处理内皮细胞会导致缩醛磷脂受到优先攻击。综上所述,缩醛磷脂酰胆碱比磷脂酰胆碱更易被氧化,并导致产生LPC-ClOH。