Hoff H F, Titus J L, Bajardo R J, Jackson R L, Gotto A M, DeBakey M E, Lie J T
Arch Pathol. 1975 May;99(5):253-8.
Using immunofluorescence techniques, apoLDL, the major protein component of human plasma low and very low density lipoproteins was localized in athersclerotic lesions from the aorta, coronary, and carotid arteries in human normolipoproteinemic, type II, and type IV hyperlipoproteinemics. Although no apoLDL was detected in uninvolved arteries, atheromas from advanced lesions as well as certain collagen and elastic fibers from both fatty streaks and advanced lesions were positive for apoLDL. This localization pattern was the same in each lipemic group, except for the presence of apoLDL in some intimal cells from type II cases. However, extensiveness of apoLDL localization was greatest in the type II group, but equal in the normolipemic and type II group. This may be explained by the high concentration gradient between plasma and tissue for apoLDL in the type II group.
运用免疫荧光技术,载脂蛋白低密度脂蛋白(apoLDL),即人血浆低密度和极低密度脂蛋白的主要蛋白质成分,在正常脂蛋白血症、II型和IV型高脂蛋白血症患者的主动脉、冠状动脉和颈动脉的动脉粥样硬化病变中定位。尽管在未受累动脉中未检测到apoLDL,但晚期病变的粥样斑块以及脂肪条纹和晚期病变中的某些胶原纤维和弹性纤维对apoLDL呈阳性反应。除了II型病例的一些内膜细胞中存在apoLDL外,这种定位模式在每个血脂异常组中都是相同的。然而,apoLDL定位的广泛程度在II型组中最大,但在正常脂蛋白血症组和IV型组中相等。这可能是由于II型组中血浆和组织之间apoLDL的高浓度梯度所致。