Glomset J A, Nichols A V, Norum K R, King W, Forte T
J Clin Invest. 1973 May;52(5):1078-92. doi: 10.1172/JCI107273.
Plasma lipoproteins of d<1.006 g/ml, d 1.006-1.019 g/ml, and d 1.019-1.063 g/ml from patients with familial lecithin:cholesterol acyltransferase deficiency yielded abnormal subfractions upon being separately filtered through 2% agarose gel. A subfraction that emerged with the void volume and contained unusually large amounts of unesterified cholesterol and phosphatidylcholine was present in each lipoprotein group, and in each group this subfraction was less prominent in the nonlipemic plasma of one patient than in the lipemic plasma of other patients. A subfraction containing smaller lipoproteins also was present in each lipoprotein group. These lipoproteins were of the same size as normal lipoproteins of the corresponding density, but contained abnormally small amounts of cholesteryl ester. The lipoproteins of 1.019-1.063 g/ml contained abnormal components of intermediate molecular weight as well as large and small abnormal components similar to those described previously. The intermediate components were more prominent in the nonlipemic plasma but were easily recognized in the hyperlipemic plasma as a peak of S(f) 20-30 in the analytical ultracentrifuge. Also they could be recognized, upon electron microscopy of the lipoproteins of d 1.019-1.063 g/ml, as particles 340-1000 A in diameter. The data suggest that related large, abnormal particles pervade the patients' very low and low density lipoproteins, and that the large particles are affected by, but are not dependent on, the lipemia that frequently accompanies the disease. The smaller very low and low density lipoproteins appear to be counterparts of lipoproteins present in normal plasma. Their abnormal composition is compatible with the possibility that lecithin:cholesterol acyltransferase normally decreases the triglyceride and phosphatidylcholine and increases the cholesteryl ester of very low density and low density plasma lipoproteins in vivo.
胆固醇酰基转移酶缺乏症患者的密度小于1.006 g/ml、1.006 - 1.019 g/ml和1.019 - 1.063 g/ml的血浆脂蛋白,在分别通过2%琼脂糖凝胶过滤后产生了异常亚组分。每个脂蛋白组中都存在一个与空体积一起出现且含有异常大量未酯化胆固醇和磷脂酰胆碱的亚组分,并且在每个组中,该亚组分在一名患者的非脂血血浆中比在其他患者的脂血血浆中不那么突出。每个脂蛋白组中还存在一个包含较小脂蛋白的亚组分。这些脂蛋白与相应密度的正常脂蛋白大小相同,但胆固醇酯含量异常少。密度为1.019 - 1.063 g/ml的脂蛋白含有中等分子量的异常组分以及与先前描述的大小异常的组分相似的大、小异常组分。中等组分在非脂血血浆中更突出,但在高脂血血浆中通过分析超速离心很容易识别为S(f) 20 - 30的峰。此外,在对密度为1.019 - 1.063 g/ml的脂蛋白进行电子显微镜检查时,可以将它们识别为直径为340 - 1000 Å的颗粒。数据表明,相关的大的异常颗粒遍布患者的极低密度和低密度脂蛋白,并且这些大颗粒受该疾病常伴随的脂血症影响,但不依赖于脂血症。较小的极低密度和低密度脂蛋白似乎是正常血浆中存在的脂蛋白的对应物。它们异常的组成与卵磷脂:胆固醇酰基转移酶在体内通常降低极低密度和低密度血浆脂蛋白的甘油三酯和磷脂酰胆碱并增加胆固醇酯的可能性相符。