Adelman S J, St Clair R W
Department of Pathology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, NC 27103.
J Lipid Res. 1988 May;29(5):643-56.
The presence of specific receptors for the metabolism of acetylated low density lipoprotein (AcLDL) and beta-migrating very low density lipoprotein (beta-VLDL) was demonstrated in thioglycolate-elicited peritoneal macrophages from both atherosclerosis-susceptible White Carneau (WC) and resistant Show Racer (SR) pigeons. Macrophages from both breeds metabolized AcLDL through a single class of receptors that were similar, but not identical, to the scavenger receptors described in mammalian macrophages. Both pigeon and mammalian AcLDL bound to this receptor. At 37 degrees C, AcLDL was internalized and degraded in the lysosomes, and cholesterol esterification and cholesteryl ester accumulation were stimulated. As in mammalian macrophages, AcLDL receptor activity was not down-regulated by cholesterol loading. In contrast, AcLDL binding was poorly competed for by fucoidin or polyinosinic acid, and the magnitude of cholesteryl ester accumulation was only about one-half of that seen with mouse peritoneal macrophages. Pigeon beta-VLDL bound to both a high and a low affinity site on pigeon macrophages. Binding to the high affinity site was calcium-dependent, pronase-sensitive, and down-regulated by cholesterol loading. Cholesterol esterification and cholesteryl ester accumulation with beta-VLDL were stimulated to an equal or greater extent than with AcLDL. Unlike mammalian macrophages, the pigeon beta-VLDL receptor did not require apolipoprotein E, as evidenced by the lack of apoE in pigeon lipoproteins and by the failure of rabbit beta-VLDL, containing apoE, to compete for binding. Pigeon LDL, but not mammalian LDL, was recognized by the pigeon beta-VLDL receptor, suggesting that like the mammalian beta-VLDL receptor, the pigeon beta-VLDL receptor may be a form of an LDL receptor. This was an unexpected finding since pigeon fibroblasts and smooth muscle cells in culture do not express LDL receptors. Thus, pigeon macrophages have receptors for the uptake of abnormal lipoproteins that could play a role in the development of macrophage-derived foam cells that are prevalent in the early stages of atherosclerosis in this species. No quantitative or qualitative differences in these receptors, however, were identified that could account for the differences in atherosclerosis susceptibility between the WC and SR breeds.
在动脉粥样硬化易感性白卡诺(WC)鸽和抗性赛鸽(SR)鸽的巯基乙酸盐诱导的腹腔巨噬细胞中,证实了存在用于乙酰化低密度脂蛋白(AcLDL)和β迁移极低密度脂蛋白(β-VLDL)代谢的特异性受体。两个品种的巨噬细胞都通过一类单一的受体代谢AcLDL,这类受体与哺乳动物巨噬细胞中描述的清道夫受体相似,但并不完全相同。鸽和哺乳动物的AcLDL都能与该受体结合。在37℃时,AcLDL被内化并在溶酶体中降解,同时刺激胆固醇酯化和胆固醇酯积累。与哺乳动物巨噬细胞一样,胆固醇负载不会下调AcLDL受体活性。相比之下,岩藻糖或聚肌苷酸对AcLDL结合的竞争性较弱,胆固醇酯积累的程度仅约为小鼠腹腔巨噬细胞的一半。鸽β-VLDL与鸽巨噬细胞上的高亲和力和低亲和力位点都能结合。与高亲和力位点的结合依赖于钙,对链霉蛋白酶敏感,且会被胆固醇负载下调。β-VLDL诱导的胆固醇酯化和胆固醇酯积累比AcLDL诱导的受到同等程度或更大程度的刺激。与哺乳动物巨噬细胞不同,鸽β-VLDL受体不需要载脂蛋白E,这一点在鸽脂蛋白中缺乏载脂蛋白E以及含有载脂蛋白E的兔β-VLDL无法竞争结合中得到了证明。鸽低密度脂蛋白(LDL)能被鸽β-VLDL受体识别,但哺乳动物LDL不能,这表明与哺乳动物β-VLDL受体一样,鸽β-VLDL受体可能是LDL受体的一种形式。这是一个意外的发现,因为培养的鸽成纤维细胞和平滑肌细胞不表达LDL受体。因此,鸽巨噬细胞具有摄取异常脂蛋白的受体,这些受体可能在该物种动脉粥样硬化早期普遍存在的巨噬细胞源性泡沫细胞的形成中发挥作用。然而,未发现这些受体在数量或质量上存在差异,无法解释WC和SR品种之间动脉粥样硬化易感性的差异。