Mori T, Takahashi K, Naito M, Kodama T, Hakamata H, Sakai M, Miyazaki A, Horiuchi S, Ando M
Second Department of Pathology, Kumamoto University School of Medicine, Japan.
Lab Invest. 1994 Sep;71(3):409-16.
The scavenger receptors are trimeric membrane glycoproteins present on the surface membrane of macrophages and macrophage-derived foam cells and are implicated in the deposition of cholesterol in the arterial walls during atherogenesis. This receptor mediates endocytosis of a diverse alley of negatively charged macromolecules including modified low density lipoproteins.
We tried biochemical and morphologic approaches to elucidate in more detail the endocytic and intracellular pathway of the scavenger receptors during endocytosis of acetylated low density lipoproteins (AcLDL) and oxidized LDL (OxLDL) by bovine alveolar macrophages. Biochemically, cell interaction and subsequent intracellular degradation of AcLDL and OxLDL were examined using [125I]AcLDL or [125I]OxLDL. At the ultramorphologic level, the scavenger receptors were detected by a mouse monoclonal antibody against bovine macrophages, D2, with colloidal gold particles (AcLDL-Au or OxLDL-Au particles) as tracer of ligands.
The biochemical studies demonstrated that after binding of AcLDL and OxLDL to the cell surface, these ligands were internalized and degraded intracellularly. Immunoelectron microscopy revealed that after a 2-hour incubation at 4 degrees C AcLDL-Au or OxLDL-Au particles were bound to the scavenger receptors present on the cell surfaces. Upon a temperature shift from 4 to 37 degrees C, these particles were concentrated in coated pits and internalized in endosomes. After subsequent dissociation of the particles from the receptors within the endosomes, the ligands were transported to secondary lysosomes, the receptors were transported to a trans-Golgi system. In the Golgi complex, the receptors were packed in secretory vesicles and recycled to the cell surface membrane. The transport and recycling of the receptors via the trans-Golgi system were completely inhibited by incubation below 18 degrees C or pretreatment with monensin.
These results suggest that during endocytosis of modified low density lipoprotein, the Golgi complex plays a crucial role in sorting and recycling of the scavenger receptors in macrophages.
清道夫受体是存在于巨噬细胞和巨噬细胞源性泡沫细胞表面膜上的三聚体膜糖蛋白,在动脉粥样硬化形成过程中与胆固醇在动脉壁中的沉积有关。该受体介导多种带负电荷的大分子(包括修饰的低密度脂蛋白)的内吞作用。
我们尝试采用生化和形态学方法,更详细地阐明牛肺泡巨噬细胞在摄取乙酰化低密度脂蛋白(AcLDL)和氧化低密度脂蛋白(OxLDL)过程中清道夫受体的内吞和细胞内途径。在生化方面,使用[125I]AcLDL或[125I]OxLDL检测AcLDL和OxLDL与细胞的相互作用以及随后在细胞内的降解。在超微形态学水平上,用抗牛巨噬细胞的小鼠单克隆抗体D2,以胶体金颗粒(AcLDL-Au或OxLDL-Au颗粒)作为配体示踪剂来检测清道夫受体。
生化研究表明,AcLDL和OxLDL与细胞表面结合后,这些配体被内化并在细胞内降解。免疫电子显微镜显示,在4℃孵育2小时后,AcLDL-Au或OxLDL-Au颗粒与细胞表面的清道夫受体结合。当温度从4℃升至37℃时,这些颗粒集中在有被小窝中并被内吞进内体。在颗粒随后在内体内与受体解离后,配体被转运至次级溶酶体,受体则被转运至反式高尔基体系统。在高尔基体复合体中,受体被包装进分泌小泡并循环至细胞表面膜。通过反式高尔基体系统对受体的转运和循环在18℃以下孵育或用莫能菌素预处理时被完全抑制。
这些结果表明,在修饰的低密度脂蛋白内吞过程中,高尔基体复合体在巨噬细胞清道夫受体的分选和循环中起关键作用。