出版社：American Society for Biochemistry and Molecular Biology
摘要：12( S )-hydroxyheptadeca-5 Z ,8 E ,10 E -trienoic acid (12-HHT) has long been considered a by-product of thromboxane A2 (TxA2) biosynthesis with no biological activity. Recently, we reported 12-HHT to be an endogenous ligand for BLT2, a low-affinity leukotriene B4 receptor. To delineate the biosynthetic pathway of 12-HHT, we established a method that enables us to quantify various eicosanoids and 12-HHT using LC-MS/MS analysis. During blood coagulation, 12-HHT levels increased in a time-dependent manner and were relatively higher than those of TxB2, a stable metabolite of TxA2. TxB2 production was almost completely inhibited by treatment with ozagrel, an inhibitor of TxA synthase (TxAS), while 12-HHT production was inhibited by 80–90%. Ozagrel-treated blood also exhibited accumulation of PGD2 and PGE2, possibly resulting from the shunting of PGH2 into synthetic pathways for these prostaglandins. In TxAS-deficient mice, TxB2 production during blood coagulation was completely lost, but 12-HHT production was reduced by 80–85%. HEK293 cells transiently expressing TxAS together with cyclooxygenase (COX)-1 or COX-2 produced both TxB2 and 12-HHT from arachidonic acid, while HEK293 cells expressing only COX-1 or COX-2 produced significant amounts of 12-HHT but no TxB2. These results clearly demonstrate that 12-HHT is produced by both TxAS-dependent and TxAS-independent pathways in vitro and in vivo.
关键词：12-HHT ; cyclooxygenase ; TxAS ; mass spectrometry ; eicosanoid
