Pan Meihui, Liang Js Jun-shan, Fisher Edward A, Ginsberg Henry N
Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
J Biol Chem. 2002 Feb 8;277(6):4413-21. doi: 10.1074/jbc.M107460200. Epub 2001 Nov 9.
Although microsomal triglyceride transfer protein (MTP) and newly synthesized triglyceride (TG) are critical for co-translational targeting of apolipoprotein B (apoB100) to lipoprotein assembly in hepatoma cell lines, their roles in the later stages of lipoprotein assembly remain unclear. Using N-acetyl-Leu-Leu-norleucinal to prevent proteasomal degradation, HepG2 cells were radiolabeled and chased for 0-90 min (chase I). The medium was changed and cells chased for another 150 min (chase II) in the absence (control) or presence of Pfizer MTP inhibitor CP-10447 (CP). As chase I was extended, inhibition of apoB100 secretion by CP during chase II decreased from 75.9% to only 15% of control (no CP during chase II). Additional studies were conducted in which chase I was either 0 or 90 min, and chase II was in the presence of [(3)H]glycerol and either BSA (control), CP (inhibits both MTP activity and TG synthesis),BMS-1976360-1) (BMS) (inhibits only MTP activity), or triacsin C (TC) (inhibits only TG synthesis). When chase I was 0 min, CP, BMS, and TC reduced apoB100 secretion during chase II by 75.3, 73.9, and 53.9%. However, when chase I was 90 min, those agents reduced apoB100 secretion during chase II by only 16.0, 19.2, and 13.9%. Of note, all three inhibited secretion of newly synthesized TG during chase II by 80, 80, and 40%, whether chase I was 0 or 90 min. In both HepG2 cells and McA-RH7777 cells, if chase I was at least 60 min, inhibition of TG synthesis and/or MTP activity did not affect the density of secreted apoB100-lipoproteins under basal conditions. Oleic acid increased secretion of TG-enriched apoB100-lipoproteins similarly in the absence or presence of either of CP, BMS, or TC. We conclude that neither MTP nor newly synthesized TG is necessary for the later stages of apoB100-lipoprotein assembly and secretion in either HepG2 or McA-RH7777 cells.
尽管微粒体甘油三酯转运蛋白(MTP)和新合成的甘油三酯(TG)对于载脂蛋白B(apoB100)在肝癌细胞系中向脂蛋白组装的共翻译靶向至关重要,但其在脂蛋白组装后期阶段的作用仍不清楚。使用N - 乙酰 - 亮氨酰 - 亮氨酰 - 正亮氨酸来防止蛋白酶体降解,对HepG2细胞进行放射性标记并追踪0 - 90分钟(追踪I)。更换培养基后,在不存在(对照)或存在辉瑞MTP抑制剂CP - 10447(CP)的情况下,将细胞再追踪150分钟(追踪II)。随着追踪I时间的延长,追踪II期间CP对apoB100分泌的抑制作用从对照(追踪II期间无CP)的75.9%降至仅15%。进行了额外的研究,其中追踪I为0或90分钟,追踪II在存在[³H]甘油和牛血清白蛋白(对照)、CP(抑制MTP活性和TG合成)、BMS - 1976360 - 1(BMS)(仅抑制MTP活性)或三辛素C(TC)(仅抑制TG合成)的条件下进行。当追踪I为分钟时,CP、BMS和TC在追踪II期间使apoB100分泌分别减少75.3%、73.9%和53.9%。然而,当追踪I为90分钟时,这些试剂在追踪II期间仅使apoB100分泌减少16.0%、19.2%和13.9%。值得注意的是,无论追踪I是0还是90分钟,这三种试剂在追踪II期间均使新合成的TG分泌减少80%、80%和40%。在HepG2细胞和McA - RH7777细胞中,如果追踪I至少为60分钟,在基础条件下抑制TG合成和/或MTP活性并不影响分泌的apoB100 - 脂蛋白的密度。在不存在或存在CP、BMS或TC中的任何一种的情况下,油酸对富含TG的apoB100 - 脂蛋白分泌的增加作用相似。我们得出结论,在HepG2细胞或McA - RH7777细胞中,MTP和新合成的TG对于apoB100 - 脂蛋白组装和分泌的后期阶段都不是必需的。