Ohta T, Ikeda Y, Hattori S, Matsuda I
Department of Pediatrics, Kumamoto University School of Medicine, Japan.
Biochim Biophys Acta. 1996 Sep 27;1303(2):137-44. doi: 10.1016/0005-2760(96)00095-1.
We investigated the effects of lipoprotein-deficient plasma (LDP) and hepatic lipase (HL) on the structure and cellular cholesterol-reducing capacity of subclasses of LpA-I (HDL containing apoA-I but not apoA-II). LpA-I is composed of large (11.1 nm; L-LpA-I), medium (8.8 nm: M-LpA-I) and small (7.7 nm: S-LpA-I) particles. L-LpA-I and M- and S-LpA-I combined (MS-LpA-I) were incubated with lipoprotein-deficient plasma and HL in the presence of very low density lipoprotein (VLDL). After incubation of L-LpA-I, the proportions of cholesteryl esters and phospholipids decreased and as a result, the proportion of protein increased. The remodeled L-LpA-I particles were generally smaller (spherical: 7.8-8.8 nm) in diameter. A small number of disc-shaped particles were also found in electron photomicrographs. These changes coincided with a slower electrophoretic mobility of remodeled L-LpA-I. In the case of MS-LpA-I, only the proportion of free cholesterol increased after incubation, and MS-LpA-I particles did not change in size. The cholesterol-reducing capacities of remodeled L-LpA-I and MS-LpA-I from macrophage foam cell were slightly higher and lower than their respective original counterparts, although neither of these differences was statistically significant. These results suggest that LDP and HL mainly contribute to the remodeling of L-LpA-I particles, and may not affect the cellular cholesterol-reducing capacity of these particles.
我们研究了脂蛋白缺乏血浆(LDP)和肝脂酶(HL)对LpA-I亚类(含有载脂蛋白A-I但不含载脂蛋白A-II的高密度脂蛋白)的结构和细胞胆固醇降低能力的影响。LpA-I由大颗粒(11.1纳米;L-LpA-I)、中颗粒(8.8纳米:M-LpA-I)和小颗粒(7.7纳米:S-LpA-I)组成。将L-LpA-I以及M-和S-LpA-I组合(MS-LpA-I)与脂蛋白缺乏血浆和HL在极低密度脂蛋白(VLDL)存在的情况下进行孵育。L-LpA-I孵育后,胆固醇酯和磷脂的比例降低,结果蛋白质比例增加。重塑后的L-LpA-I颗粒直径通常较小(球形:7.8 - 8.8纳米)。在电子显微镜照片中也发现了少量盘状颗粒。这些变化与重塑后的L-LpA-I较慢的电泳迁移率一致。对于MS-LpA-I,孵育后仅游离胆固醇比例增加,且MS-LpA-I颗粒大小未改变。来自巨噬细胞泡沫细胞的重塑后L-LpA-I和MS-LpA-I的胆固醇降低能力分别略高于和低于其各自的原始对应物,尽管这些差异均无统计学意义。这些结果表明,LDP和HL主要促成L-LpA-I颗粒的重塑,且可能不影响这些颗粒的细胞胆固醇降低能力。