Jost C R, Huizinga T W, de Goede R, Fransen J A, Tetteroo P A, Daha M R, Ginsel L A
Laboratory for Electron Microscopy, University of Leiden, The Netherlands.
Blood. 1990 Jan 1;75(1):144-51.
Immunoelectron microscopic studies in human neutrophils showed that FcRIII was present on the plasma membrane, in the Golgi complex, and in many small vesicles (120 to 180 nm). FcRIII was not found in specific or azurophilic granules as shown by immunogold double-labeling experiments, visualizing both FcRIII and either lactoferrin (a marker of specific granules) or myeloperoxidase (a marker for azurophilic granules). Because the occurrence of FcRIII in the Golgi complex suggested that biosynthesis of this receptor occurs in these cells, metabolic labeling experiments were performed. Immunoprecipitation of FcRIII from NP-40 lysates of cells labeled with 35S-methionine showed a diffuse 50- to 70-Kd band corresponding with the band noted after immunoprecipitation of FcRIII from surface iodinated cells. These findings show that de novo synthesis of FcRIII occurs in neutrophils and suggest that at least some of the small vesicles containing FcRIII derive from the Golgi complex and thus are involved in transport of newly synthesized FcRIII to the plasma membrane.
对人类中性粒细胞进行的免疫电子显微镜研究显示,FcRIII存在于质膜、高尔基体复合体以及许多小囊泡(120至180纳米)中。免疫金双标记实验表明,在特异性或嗜天青颗粒中未发现FcRIII,该实验同时观察FcRIII以及乳铁蛋白(特异性颗粒的标志物)或髓过氧化物酶(嗜天青颗粒的标志物)。由于FcRIII在高尔基体复合体中的出现提示该受体的生物合成发生在这些细胞中,因此进行了代谢标记实验。从用35S-甲硫氨酸标记的细胞的NP-40裂解物中免疫沉淀FcRIII,显示出一条弥散的50至70千道尔顿条带,与从表面碘化细胞中免疫沉淀FcRIII后观察到的条带一致。这些发现表明,FcRIII的从头合成发生在中性粒细胞中,并提示至少一些含有FcRIII的小囊泡源自高尔基体复合体,因此参与了新合成的FcRIII向质膜的转运。