Chapman M J, Goldstein S
Atherosclerosis. 1976 Nov-Dec;25(2-3):267-91. doi: 10.1016/0021-9150(76)90033-2.
The principal form of the serum low density lipoprotein (LDL) in man, baboon, rhesus monkey and pig was isolated by preparative ultracentrifugation in the density interval 1.024-1.045 g/ml. The physicochemical characteristics of pig LDL most closely resembled those of man; thus, electrophoretic studies suggested that both baboon and rhesus LDL have a greater surface charge than that of their human counterpart, and electron-microscopic investigations showed baboon LDL (245 A) to be larger and rhesus LDL (205 A) smaller than those of man (217 A) and pig (228 A). In contrast, the immunological relationship between LDL from the two Old World monkeys and that of man was much closer (80-85% cross-reactivity by micro-immunoprecipitation) than that between pig and man (35% cross-reactivity). The principal difference between pig and human LDL appeared to reside in their protein and carbohydrate moieties. There was a marked resemblance between the protein moieties (apo-LDL) of LDL from the four species. The principal component of each animal apo-LDL was separated by gel-filtration chromatography and amounted to greater than 95% of the total protein; it exhibited a high molecular weight (greater than 250,000) upon SDS-polyacrylamide-gel electrophoresis and was indistinguishable from human apolipoprotein B in amino acid composition. Differences both between the apo-LDL and between the apo-B preparations from the four species, however, were detectable by immunological procedures. Such studies revealed inter-species relationships which were essentially the same as those observed between the respective native LDL preparations. The soluble apolipoproteins, present as minor components (less than 5%) of each apo-LDL, were compared by their electrophoretic mobility in polyacrylamide gel; the pattern seen in baboon and rhesus apo-LDL appeared to be most closely akin to that typical of their human counterpart. It is apparent that many characteristics typical of human serum LDL are found in those of the pig, rhesus monkey and baboon. Moreover, in view of the striking relationship existing between the immunological properties and apo-protein components of the LDL of the two Old World monkeys and that of man, these subhuman primates appear to be highly suitable as animal models for experimental atherosclerosis.
通过在密度区间1.024 - 1.045 g/ml进行制备性超速离心,分离出了人类、狒狒、恒河猴和猪血清中低密度脂蛋白(LDL)的主要形式。猪LDL的物理化学特性与人类的最为相似;因此,电泳研究表明,狒狒和恒河猴的LDL表面电荷均比人类LDL的表面电荷多,而电子显微镜研究显示,狒狒LDL(245 Å)比人类(217 Å)和猪(228 Å)的LDL大,恒河猴LDL(205 Å)比人类和猪的LDL小。相比之下,两种旧世界猴的LDL与人类LDL之间的免疫关系(通过微量免疫沉淀法检测,交叉反应率为80 - 85%)比猪与人类LDL之间的免疫关系(交叉反应率为35%)更为密切。猪和人类LDL的主要差异似乎存在于它们的蛋白质和碳水化合物部分。四种动物LDL的蛋白质部分(载脂蛋白LDL)之间有显著的相似性。每种动物载脂蛋白LDL的主要成分通过凝胶过滤色谱法分离,占总蛋白的比例超过95%;在SDS - 聚丙烯酰胺凝胶电泳中,它表现出高分子量(大于250,000),并且在氨基酸组成上与人类载脂蛋白B无法区分。然而,通过免疫程序可以检测到四种动物的载脂蛋白LDL之间以及载脂蛋白B制剂之间的差异。此类研究揭示的种间关系与各自天然LDL制剂之间观察到的种间关系基本相同。通过它们在聚丙烯酰胺凝胶中的电泳迁移率对作为每种载脂蛋白LDL次要成分(小于5%)存在的可溶性载脂蛋白进行了比较;在狒狒和恒河猴载脂蛋白LDL中看到的模式似乎与人类对应物的典型模式最为相似。显然,人类血清LDL的许多典型特征在猪、恒河猴和狒狒的血清LDL中也能找到。此外,鉴于两种旧世界猴的LDL与人类LDL在免疫特性和载脂蛋白成分之间存在显著关系,这些灵长类动物似乎非常适合作为实验性动脉粥样硬化的动物模型。