Steinmetz A
SERLIA, Institut Pasteur, Lille.
Ann Biol Clin (Paris). 1991;49(1):1-8.
There is agreement about the influence of the genetic apolipoprotein (apo E) polymorphism on plasma lipid and apoprotein levels in man. Whereas the association of the apo E2 isoform with primary dysbetalipoproteinemia and hyperlipoproteinemia type III is well established, the plasma- and LDL-cholesterol lowering effects of apo E2 and the phenomenon of apo E4 raising these parameters on the development of coronary heart disease is still a matter of controversial discussion. Despite these uncertainties the knowledge of an individual's apo E phenotype may provide additional information in future to judge its risk to develop atherosclerosis. From a variety of methods meanwhile described to analyze the polymorphism and evaluate the apo E phenotype the author has modified three procedures to apply to different questions concerning apo E isoform analysis. They concern the visualization of the apo E pattern in diluted solutions and those containing high salt concentrations, the apo E phenotyping on a large scale basis from whole plasma avoiding a possible misinterpretation by a thrombin fragment of apo E and finally the search for new apo E variants with a high resolution system on immobilized pH gradient gels.
关于遗传性载脂蛋白(apo E)多态性对人体血浆脂质和载脂蛋白水平的影响已达成共识。虽然apo E2亚型与原发性异常β脂蛋白血症和III型高脂蛋白血症之间的关联已得到充分证实,但apo E2降低血浆和低密度脂蛋白胆固醇的作用以及apo E4升高这些参数对冠心病发展的影响仍存在争议。尽管存在这些不确定性,但了解个体的apo E表型在未来可能会为判断其发生动脉粥样硬化的风险提供额外信息。在目前描述的用于分析多态性和评估apo E表型的各种方法中,作者改进了三种方法,以应用于与apo E亚型分析相关的不同问题。它们涉及在稀释溶液和高盐浓度溶液中apo E模式的可视化,从全血大规模进行apo E表型分析以避免apo E凝血酶片段可能造成的错误解读,以及最终在固定化pH梯度凝胶上使用高分辨率系统寻找新的apo E变体。