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凝集素诱导的人血小板氧化应激。

Lectin-induced oxidative stress in human platelets.

机构信息

Department of Pharmacy, Biochemistry Lab, University of Genoa, Genova, 16132, Italy.

Department of Experimental Medicine, University of Genoa, Genova, 16132, Italy.

出版信息

Redox Biol. 2020 May;32:101456. doi: 10.1016/j.redox.2020.101456. Epub 2020 Feb 8.

DOI:10.1016/j.redox.2020.101456
PMID:32063518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7264469/
Abstract

Previously we have shown that wheat germ agglutinin (WGA) and, with minor potency, Phaseolus vulgaris agglutinin (PHA), but not lens culinarian agglutinin (LCA), induce platelet aggregation, through the PLCƴ2 activation by the concerted action of src/syk and PI3K/BTK pathways. In this study, we have investigated platelet oxidative stress induced by lectins. Several parameters indicative of oxidative stress, such as reactive oxygen species (ROS), superoxide anion, lipid peroxidation and the efficiency of the aerobic metabolism, have been measured. It was found that ROS, superoxide anion formation and lipid peroxidation are significantly increased upon platelet treatment with WGA and PHA while LCA is ineffective. WGA is always more effective than PHA in all experimental conditions tested. In addition, the involvement of NADPH oxidase 1, syk and PI3K in oxidative stress induced by WGA and PHA has been shown. Concerning the lectins effect on aerobic metabolism, WGA and PHA, but not LCA, act as uncoupling agents, determining an increase of oxygen consumption and a decrease of ATP synthesis, with a consequent decrease of P/O value. These results are confirmed by the impairment of platelets proton gradient formation, evaluated by membrane potential, in platelets treated with WGA and PHA. In conclusion lectins, especially WGA, induce oxidative stress in platelets and decrease energy availability through modifications of membrane structure leading to the inefficiency of the aerobic machinery that steers platelets toward death as suggested by the decreased metabolic activity of platelets and the increased lactic dehydrogenase release.

摘要

先前我们已经证明,麦胚凝集素(WGA)和菜豆凝集素(PHA),虽然效力较小,但不会引起晶状体凝集素(LCA),能够通过 src/syk 和 PI3K/BTK 通路的协同作用激活 PLCγ2 诱导血小板聚集。在这项研究中,我们研究了凝集素诱导的血小板氧化应激。已经测量了几个指示氧化应激的参数,如活性氧(ROS)、超氧阴离子、脂质过氧化和有氧代谢的效率。结果发现,WGA 和 PHA 处理血小板会显著增加 ROS、超氧阴离子形成和脂质过氧化,而 LCA 则无效。在所有测试的实验条件下,WGA 始终比 PHA 更有效。此外,还表明 NADPH 氧化酶 1、syk 和 PI3K 参与了 WGA 和 PHA 诱导的氧化应激。关于凝集素对有氧代谢的影响,WGA 和 PHA,但不是 LCA,作为解偶联剂,导致耗氧量增加和 ATP 合成减少,从而导致 P/O 值降低。这些结果通过膜电位评估 WGA 和 PHA 处理的血小板中质子梯度形成的损伤得到证实。总之,凝集素,特别是 WGA,会诱导血小板发生氧化应激,并通过改变膜结构降低能量供应,从而导致有氧代谢机制效率降低,使血小板走向死亡,正如血小板代谢活性降低和乳酸脱氢酶释放增加所表明的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/d28bc945a8a5/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/b8adc0c6490b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/4ed73227fae0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/196ee56ff14f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/df83b6bfb3d4/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/93b9656c0198/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/f92c9cc4b454/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/fa5bde17ab50/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/bb69356c6c46/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/37b88b530758/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/d28bc945a8a5/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/b8adc0c6490b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/4ed73227fae0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/196ee56ff14f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/df83b6bfb3d4/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/93b9656c0198/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/f92c9cc4b454/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/fa5bde17ab50/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/bb69356c6c46/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/37b88b530758/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/7264469/d28bc945a8a5/gr10.jpg

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