Nakao J, Ooyama T, Ito H, Chang W C, Murota S
Atherosclerosis. 1982 Sep;44(3):339-42. doi: 10.1016/0021-9150(82)90008-9.
We investigated the effects of mono-hydroxyeicosatetraenoic acids (HETEs) and N-formyl-methionyl-leucyl-phenylalanine (F-Met-Leu-Phe) on rat aortic smooth muscle cell migration in modified Boyden chambers. 12-HETE showed the most potent stimulatory effect on smooth muscle cell migration among the mono-HETEs tested. The optimal concentrations for cell migration were 3 X 10(-15) and 3 X 10(-13) g/ml for 12-HETE and 10(-8) g/ml for 15-HETE, 5-HETE and F-Met-Leu-Phe were inactive with these cells. As 12-HETE is biosynthesized from arachidonic acid by the 12-lipoxygenase pathway in platelets and macrophages, and 15-HETE by the 15-lipoxygenase pathway in granulocytes, the present results indicate an important role for such cells in the early phase of atherosclerosis.
我们在改良的博伊登小室中研究了单羟基二十碳四烯酸(HETEs)和N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(F-Met-Leu-Phe)对大鼠主动脉平滑肌细胞迁移的影响。在所测试的单羟基HETEs中,12-HETE对平滑肌细胞迁移显示出最有效的刺激作用。12-HETE促进细胞迁移的最佳浓度为3×10⁻¹⁵和3×10⁻¹³g/ml,15-HETE、5-HETE和F-Met-Leu-Phe的最佳浓度为10⁻⁸g/ml,5-HETE和F-Met-Leu-Phe对这些细胞无活性。由于12-HETE是由血小板和巨噬细胞中的花生四烯酸通过12-脂氧合酶途径生物合成的,而15-HETE是由粒细胞中的15-脂氧合酶途径生物合成的,目前的结果表明这些细胞在动脉粥样硬化早期阶段具有重要作用。