Assembly of rat hepatic very low density lipoproteins in the endoplasmic reticulum.
نویسندگان
چکیده
The intracellular site of assembly of hepatic very low density lipoproteins has been investigated. Two endoplasmic reticulum fractions and Golgi vesicles (relatively free from endosomal contamination) were isolated from rat liver and the luminal contents were released. The apoB-containing entities were separated from the lumen of the endoplasmic reticulum and Golgi vesicles by an immunoaffinity isolation procedure. The amount of each lipid moiety (triacylglycerols, cholesterol plus cholesteryl esters and phospholipids) associated with a unit mass of apoB was shown to be very similar in the luminal contents isolated from each of the three fractions. Moreover, the apoB-containing particles that were isolated from the endoplasmic reticulum and Golgi were mainly present in a fraction of density < 1.02 g/ml. The average diameter of these lipoprotein particles was shown by negative staining electron microscopy to be in the size range of very low density lipoproteins and low density lipoproteins. The size and composition of the intracellular lipoproteins were very similar to those of both very low density lipoproteins isolated from the culture medium from rat hepatocytes and plasma very low density lipoproteins. The conclusion from this study is that the full complement of lipids associate with apoB at an early stage during the secretory pathway, in the endoplasmic reticulum.
منابع مشابه
The Effect of Zinc Deficiency and Food Restriction on Hepatic Zinc Proteins in the Rat
found in the response of the electron-capture detector for fatty acids of niicrosomal lipids from CC1,-treated rats (the latter peak is clearly a group of unresolved peaks). Since serum very-low-density lipoproteins derive directly from the hepatic cell and since the phospholipid fraction of such lipoproteins is believed to derive from the phospholipids of the endoplasmic reticulum, we investig...
متن کاملAssembly of very low density lipoproteins in rat liver: a study of nascent particles recovered from the rough endoplasmic reticulum.
To investigate the assembly pathway for hepatic very low density lipoproteins (VLDL), nascent lipoproteins were recovered from a purified, intact rough endoplasmic reticulum (ER) fraction isolated from rat liver. Two fractions were recovered by ultracentrifugation. Particles isolated at d 1.006 g/ml were triglyceride-rich particles containing apolipoprotein (apo)B-100 or apoB-48, and apoE with ...
متن کاملAssembly of very low density lipoproteins in rat
To investigate the assembly pathway for hepatic very low density lipoproteins (VLDL), nascent lipoproteins were recovered from a purified, intact rough endoplasmic reticulum (ER) fraction isolated from rat liver. Two fractions were recovered by ultracentrifugation. Particles isolated at d 1.006 g/ml were triglyceride-rich particles containing apolipoprotein (apo)B-100 or apoB-48, and apoE with ...
متن کاملApolipoprotein B100 quality control and the regulation of hepatic very low density lipoprotein secretion
Apolipoprotein B (apoB) is the main protein component of very low density lipoprotein (VLDL) and is necessary for the assembly and secretion of these triglyceride (TG)-rich particles. Following release from the liver, VLDL is converted to low density lipoprotein (LDL) in the plasma and increased production of VLDL can therefore play a detrimental role in cardiovascular disease. Increasing evide...
متن کاملIntrahepatic assembly of very low density lipoproteins. Rate of transport out of the endoplasmic reticulum determines rate of secretion.
To identify the rate-limiting step(s) in the hepatic production of very low density lipoproteins (VLDL), we investigated the intracellular distribution and rate of intracellular transport of de novo synthesized apolipoprotein B (apoB). For all secretory proteins examined (i.e. albumin, large molecular weight apoB, and small molecular weight apoB) the rough and smooth microsomes contained the ma...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 268 5 شماره
صفحات -
تاریخ انتشار 1993