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1-O-烷基-SN-甘油-3-磷酸胆碱(溶血血小板活化因子)和1-O-烯基-SN-甘油-3-磷酸乙醇胺与二十二碳六烯酸(22:6 ω-3)的转酰基作用

Transacylation of 1-O-alkyl-SN-glycero-3-phosphocholine (lyso platelet-activating factor) and 1-O-alkenyl-SN-glycero-3-phosphoethanolamine with docosahexaenoic acid (22:6 omega 3).

作者信息

Sugiura T, Masuzawa Y, Waku K

出版信息

Biochem Biophys Res Commun. 1985 Dec 17;133(2):574-80. doi: 10.1016/0006-291x(85)90944-1.

Abstract

[14C]22:6 (docosahexaenoic acid) was rapidly incorporated into cellular lipids in rabbit alveolar macrophages. After removal of free [14C]22:6, the radioactivity in diacyl-glycerophosphocholine (GPC) gradually decreased with a concomitant increase in [14C]22:6 in alkylacyl-GPC and alkenylacyl-glycerophosphoethanolamine (GPE), indicating that [14C]22:6 was transferred from diacyl-GPC to these ether lipid fractions. In fact, macrophage microsomes were shown to catalyze the transfer of [14C]22:6 from exogenously added diacyl-GPC to 1-alkyl-GPC (lyso platelet-activating factor) and 1-alkenyl-GPE. These results are the first evidence for the involvement of the transacylation system in the metabolism of C22 polyunsaturated fatty acids and lyso platelet-activating factor.

摘要

[14C]22:6(二十二碳六烯酸)迅速掺入兔肺泡巨噬细胞的细胞脂质中。去除游离的[14C]22:6后,二酰基甘油磷酸胆碱(GPC)中的放射性逐渐降低,同时烷基酰基-GPC和烯基酰基甘油磷酸乙醇胺(GPE)中[14C]22:6增加,这表明[14C]22:6从二酰基-GPC转移到了这些醚脂组分中。事实上,巨噬细胞微粒体被证明能催化[14C]22:6从外源添加的二酰基-GPC转移到1-烷基-GPC(溶血血小板活化因子)和1-烯基-GPE。这些结果首次证明了转酰基系统参与C22多不饱和脂肪酸和溶血血小板活化因子的代谢。

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