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鸡肝高密度脂蛋白的生物合成:新生脂质与载脂蛋白A1的结合。

Biosynthesis of high density lipoprotein by chicken liver: conjugation of nascent lipids with apoprotein A1.

作者信息

Banerjee D, Redman C M

出版信息

J Cell Biol. 1984 Dec;99(6):1917-26. doi: 10.1083/jcb.99.6.1917.

Abstract

To study the assembly of newly synthesized lipids with apoprotein A1, we administered [2-3H]glycerol to young chickens and determined the hepatic intracellular sites of lipid synthesis and association of nascent lipids with apoprotein A1. [2-3H]glycerol was rapidly incorporated into hepatic lipids, reaching maximal levels at 5 min, and this preceded the appearance of lipid radioactivity in the plasma. The liver was fractionated into rough and smooth endoplasmic reticulum and Golgi cell fractions. The isolated cell fractions were further subfractionated into membrane and soluble (content) fractions by treatment with 0.1 M Na2CO3, pH 11.3. At various times, the lipid radioactivity was measured in each of the intracellular organelles, in immunoprecipitable apoprotein A1, and in materials that floated at buoyant densities similar to those of plasma lipoproteins. Maximal incorporation occurred at 1 min in the rough endoplasmic reticulum, at 3-5 min in the smooth endoplasmic reticulum, and at 5 min in the Golgi cell fractions. The majority (66-93%) of radioactive glycerol was incorporated into triglycerides with smaller (4-27%) amounts into phospholipids. About 80% of the lipid radioactivity in the endoplasmic reticulum and 70% of that in the Golgi cell fractions was in the membranes. The radioactive lipids in the content subfraction were distributed in various density classes with most nascent lipids floating at a density less than or equal to 1.063 g/ml. Apoprotein A1 from the Golgi apparatus, obtained by immunoprecipitation, contained sixfold more nascent lipids than did that from the endoplasmic reticulum. These data indicate that [2-3H]glycerol is quickly incorporated into lipids of the endoplasmic reticulum and the Golgi cell fractions, that most of the nascent lipids are conjugated with apoproteins A1 in the Golgi apparatus, and that very little association of nascent lipid to apoprotein A1 occurs in the endoplasmic reticulum.

摘要

为了研究新合成的脂质与载脂蛋白A1的组装过程,我们给幼鸡注射了[2-³H]甘油,并确定了肝脏内脂质合成的细胞内位点以及新生脂质与载脂蛋白A1的结合情况。[2-³H]甘油迅速掺入肝脏脂质中,在5分钟时达到最高水平,且早于血浆中脂质放射性的出现。肝脏被分离成粗面内质网、滑面内质网和高尔基体细胞组分。通过用0.1M碳酸钠(pH 11.3)处理,将分离出的细胞组分进一步亚分离成膜组分和可溶性(内容物)组分。在不同时间,测量每个细胞内细胞器、免疫沉淀的载脂蛋白A1以及漂浮密度与血浆脂蛋白相似的物质中的脂质放射性。最大掺入量在粗面内质网中于1分钟出现,在滑面内质网中于3 - 5分钟出现,在高尔基体细胞组分中于5分钟出现。大部分(66 - 93%)放射性甘油掺入甘油三酯,少量(4 - 27%)掺入磷脂。内质网中约80%的脂质放射性以及高尔基体细胞组分中70%的脂质放射性存在于膜中。内容物亚组分中的放射性脂质分布在不同密度类别中,大多数新生脂质漂浮密度小于或等于1.063 g/ml。通过免疫沉淀从高尔基体获得的载脂蛋白A1所含新生脂质比从内质网获得的多六倍。这些数据表明,[2-³H]甘油迅速掺入内质网和高尔基体细胞组分的脂质中,大多数新生脂质在高尔基体中与载脂蛋白A1结合,而在内质网中新生脂质与载脂蛋白A1的结合很少。

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