Deckelbaum R J, Olivecrona T, Fainaru M
J Lipid Res. 1980 May;21(4):425-34.
Because we found apoprotein contamination of some high-grade commercial albumins, we studied this effect on formation of lipoprotein-like particles during lipolysis of human very low density lipoprotein (VLDL) in vitro. After a 1-hr incubation with purified bovine milk lipoprotein lipase, over 98% VLDL triglyceride was hydrolyzed in the presence of either albumin B (apoprotein-rich) or albumin C (apoprotein-poor), with a weight ratio of albumin to triglyceride of 60 to 1. Lipoproteins of density < 1.019 g/ml ("IDL"), 1.019 to 1.063 g/ml ("LDL"), and 1.063 to 1.21 g/ml ("HDL") were then isolated by ultracentrifugation. Recovery of non-triglyceride VLDL constituents in "IDL" and "LDL" was similar for albumin B or albumin C. "LDL" was the major catabolic product of in vitro VLDL lipolysis independent of the albumin used. The yield of "HDL," however, was 5- to 6-fold greater with albumin B. All lipoproteins produced with albumin B were richer in phospholipid, apoproteins C and A-I, relative to lipoproteins produced in the presence of albumin C. With albumin B, cholesterol/phospholipid molar ratios were <1 in all in vitro produced lipoproteins, but were >1 with albumin C. All these differences can be ascribed to the presence in albumin B of 0.2 mg apoprotein A-I/g albumin and 1.8 mg phospholipid/g albumin; these components were not detected in albumin C. Thus, two thirds of "HDL" recovered with VLDL lipolysis in the presence of albumin B can be accounted for by albumin itself and only one third from constituents of VLDL. Adding equivalent amounts of both apoproteins removed from albumin B and phospholipid to albumin C markedly decreased the disparities in results but addition of each alone did not. These results prove "inert" albumins serve other than as fatty acid and lysolecithin acceptors in in vitro model systems, and do influence formation of lipoproteins during in vitro VLDL catabolism.-Deckelbaum, R. J., T. Olivecrona, and M. Fainaru. The role of different albumin preparations on production of human plasma lipoprotein-like particles in vitro.
由于我们发现一些高纯度商业白蛋白存在载脂蛋白污染,因此我们研究了其在体外人极低密度脂蛋白(VLDL)脂解过程中对脂蛋白样颗粒形成的影响。在用纯化的牛乳脂蛋白脂肪酶孵育1小时后,在存在白蛋白B(富含载脂蛋白)或白蛋白C(贫载脂蛋白)的情况下,超过98%的VLDL甘油三酯被水解,白蛋白与甘油三酯的重量比为60比1。然后通过超速离心分离出密度<1.019 g/ml(“IDL”)、1.019至1.063 g/ml(“LDL”)和1.063至1.21 g/ml(“HDL”)的脂蛋白。白蛋白B或白蛋白C在“IDL”和“LDL”中非甘油三酯VLDL成分的回收率相似。“LDL”是体外VLDL脂解的主要分解代谢产物,与所用的白蛋白无关。然而,白蛋白B存在时“HDL”的产量高出5至6倍。相对于白蛋白C存在时产生的脂蛋白,白蛋白B产生的所有脂蛋白中磷脂、载脂蛋白C和A-I更丰富。使用白蛋白B时,所有体外产生的脂蛋白中胆固醇/磷脂摩尔比<1,但使用白蛋白C时则>1。所有这些差异可归因于白蛋白B中存在0.2 mg载脂蛋白A-I/g白蛋白和1.8 mg磷脂/g白蛋白;在白蛋白C中未检测到这些成分。因此,在白蛋白B存在下VLDL脂解回收的“HDL”中,三分之二可由白蛋白本身解释,只有三分之一来自VLDL成分。向白蛋白C中添加从白蛋白B中去除的等量载脂蛋白和磷脂可显著降低结果差异,但单独添加每种成分则不会。这些结果证明,在体外模型系统中,“惰性”白蛋白的作用不仅仅是作为脂肪酸和溶血卵磷脂的受体,而且确实会影响体外VLDL分解代谢过程中脂蛋白的形成。——德克尔鲍姆,R. J.,T. 奥利维克罗纳,和M. 法伊纳鲁。不同白蛋白制剂在体外人血浆脂蛋白样颗粒产生中的作用。