Müller K, Hardwick S J, Marchant C E, Law N S, Waeg G, Esterbauer H, Carpenter K L, Mitchinson M J
Division of Cellular Pathology, University of Cambridge, UK.
FEBS Lett. 1996 Jun 17;388(2-3):165-8. doi: 10.1016/0014-5793(96)00559-5.
We have investigated the cytotoxic and chemotactic potencies of malondialdehyde (MDA), hexanal, 4-hydroxyhexenal (HHE), 4-hydroxynonenal (HNE) and 4-hydroxyoctenal (HOE), which are aldehydes found in oxidised low density lipoprotein (LDL), for human monocyte-macrophages. They were toxic in the following order: hexanal<HHE= HOE< HNE. HNE was toxic at 20 microM and chemotactic at 2.5 microM. The other aldehydes tested had no chemoattractant activity. Our results suggest that HNE arising from LDL oxidation could attract monocytes into the human atherosclerotic lesion. A direct cytotoxic role of aldehydes in foam cell death in the lesion is less likely.
我们研究了丙二醛(MDA)、己醛、4-羟基己烯醛(HHE)、4-羟基壬烯醛(HNE)和4-羟基辛烯醛(HOE)对人单核细胞-巨噬细胞的细胞毒性和趋化活性,这些醛类存在于氧化型低密度脂蛋白(LDL)中。它们的毒性顺序如下:己醛<HHE = HOE<HNE。HNE在20微摩尔时具有毒性,在2.5微摩尔时具有趋化性。所测试的其他醛类没有趋化活性。我们的结果表明,LDL氧化产生的HNE可能会将单核细胞吸引到人类动脉粥样硬化病变中。醛类在病变中泡沫细胞死亡方面的直接细胞毒性作用可能性较小。