Field W E, Ferguson F G, Reddanna P, Reddy C C
Pennsylvania State University, Department of Veterinary Science, University Park 16802.
Prostaglandins. 1988 Oct;36(4):411-9. doi: 10.1016/0090-6980(88)90039-1.
The effect of arachidonic acid (AA) metabolites of lipoxygenase(s) was evaluated on natural killer (NK) cell activity in Fischer F344 rat splenic lymphocytes and compared with prostaglandin E2 (PGE2), a known inhibitor of NK cell lytic activity. It was observed that 5(S),12(S)-dihydroxy-6,10-trans-8,14-cis-eicosatetraenoic acid (5(S),12(S)-diHETE, EZEZ) inhibited NK cell activity to a degree comparable to the inhibitory effects of PGE2. This compound maximally inhibited NK cell activity at concentrations of 10(-6) and 10(-8) M. PGE2 and 5(S),12(S)-diHETE (EZEZ) inhibited NK activity to an identical degree at all concentrations and effector:target (E:T) cell ratios tested. Of the other lipoxygenase pathway metabolites screened, 8(S),15(S)-all trans-diHETE and 8(S),15(S)-diHETE (EZEZ) also inhibited NK activity, but only at 10(-6) M and a 50:1 E:T cell ratio. These findings provide further evidence that the lipoxygenase and cyclooxygenase pathways produce metabolites which can modulate NK cell function, and that 5(S),12(S)-diHETE (EZEZ), which has not been previously tested for effects on NK cells, may have a significant immunoregulatory role.
评估了脂氧合酶的花生四烯酸(AA)代谢产物对Fischer F344大鼠脾淋巴细胞中自然杀伤(NK)细胞活性的影响,并与已知的NK细胞裂解活性抑制剂前列腺素E2(PGE2)进行了比较。观察到5(S),12(S)-二羟基-6,10-反式-8,14-顺式-二十碳四烯酸(5(S),12(S)-二氢二十碳四烯酸,EZEZ)对NK细胞活性的抑制程度与PGE2的抑制作用相当。该化合物在浓度为10^(-6)和10^(-8) M时最大程度地抑制了NK细胞活性。在所有测试的浓度和效应细胞:靶细胞(E:T)比例下,PGE2和5(S),12(S)-二氢二十碳四烯酸(EZEZ)对NK活性的抑制程度相同。在筛选的其他脂氧合酶途径代谢产物中,8(S),15(S)-全反式-二氢二十碳四烯酸和8(S),15(S)-二氢二十碳四烯酸(EZEZ)也抑制了NK活性,但仅在10^(-6) M和50:1的E:T细胞比例下。这些发现进一步证明脂氧合酶和环氧化酶途径产生的代谢产物可以调节NK细胞功能,并且之前未测试过对NK细胞影响的5(S),12(S)-二氢二十碳四烯酸(EZEZ)可能具有重要的免疫调节作用。