Brouwers J F, Van Hellemond J J, van Golde L M, Tielens A G
Laboratory of Veterinary Biochemistry and Institute of Biomembranes, Utrecht University, The Netherlands.
Mol Biochem Parasitol. 1998 Oct 30;96(1-2):49-58. doi: 10.1016/s0166-6851(98)00103-0.
Schistosomes have lost the capability to synthesize fatty acids de novo, but they can modify fatty acids by chain elongation. This has a profound effect on the molecular species composition of the two main phospholipid fractions of schistosomes, phosphatidylcholine (PC) and phosphatidylethanolamine (PE). Molecular species of phospholipids are increasingly recognized as important mediators, or precursors thereof, in signal transduction, immune response modulation, and events like membrane fusion. As these are all important aspects of schistosome membranes and of the tegumental membranes in particular, we analysed the PE and PC molecular species of the tegumental membranes, the worm body and the blood of the host. With the aid of on-line mass spectrometry, we unequivocally identified a large number of PC and PE species in schistosomes, among which considerable amounts of plasmalogen species. This was unexpected, as this lipid subclass has been assumed to be absent in the parasite. Species, like (20:1-16:0) diacyl PC and (16:0-20:1) plasmalogen PE, found to be main constituents in schistosomes, were absent from the blood of the host. Large differences were also found between the molecular species composition of the tegumental membranes and the membranes of the worm body. In the tegumental membranes, 1-hexadecyl 2-palmitoyl PC was detected, which could possibly function as a precursor for platelet activating factor (PAF).
血吸虫已经失去了从头合成脂肪酸的能力,但它们可以通过链延长来修饰脂肪酸。这对血吸虫的两种主要磷脂组分,即磷脂酰胆碱(PC)和磷脂酰乙醇胺(PE)的分子种类组成产生了深远影响。磷脂的分子种类越来越被认为是信号转导、免疫反应调节以及膜融合等过程中的重要介质或其前体。由于这些都是血吸虫膜尤其是皮层膜的重要方面,我们分析了皮层膜、虫体和宿主血液中的PE和PC分子种类。借助在线质谱分析,我们明确鉴定出了血吸虫中大量的PC和PE种类,其中有相当数量的缩醛磷脂种类。这是出乎意料的,因为一直认为这种脂质亚类在寄生虫中不存在。像(20:1-16:0)二酰基PC和(16:0-20:1)缩醛磷脂PE这样被发现是血吸虫主要成分的种类,在宿主血液中并不存在。皮层膜和虫体膜的分子种类组成之间也存在很大差异。在皮层膜中检测到了1-十六烷基2-棕榈酰PC,它可能作为血小板活化因子(PAF)的前体发挥作用。