Ehrenreich B A, Cohn Z A
J Exp Med. 1967 Nov 1;126(5):941-58. doi: 10.1084/jem.126.5.941.
Mouse peritoneal macrophages take up I*-HSA from their medium during in vitro cultivation. Conditions which promote I*-HSA uptake are the same as those which stimulate formation of pinocytic vesicles. Autoradiography of cells pulsed with (125)I-HSA showed that intracellular isotope is localized in perinuclear granules, or secondary lysosomes. Following a pulse of (125)I-HSA, intracellular radioactivity decreases and the amount of TCA-soluble isotope in the medium increases correspondingly. About 50% of the intracellular isotope is lost in 5 hr. The release of isotope from pulsed cells is not inhibited by parafluorophenylalanine, 2,4-dinitrophenol or by a reduction of the serum concentration of the medium. However, the processing of ingested (125)I-HSA is reversibly inhibited by reduced temperature. The TCA-soluble radioactive material excreted by pulsed macrophages was identified as monoiodotyrosine.
在体外培养过程中,小鼠腹腔巨噬细胞从其培养基中摄取碘标记人血清白蛋白(I*-HSA)。促进I*-HSA摄取的条件与刺激胞饮小泡形成的条件相同。用碘-125标记人血清白蛋白((125)I-HSA)脉冲处理细胞的放射自显影显示,细胞内的同位素定位于核周颗粒或次级溶酶体中。在用(125)I-HSA脉冲处理后,细胞内放射性降低,培养基中三氯乙酸可溶性同位素的量相应增加。约50%的细胞内同位素在5小时内丢失。来自脉冲处理细胞的同位素释放不受对氟苯丙氨酸、2,4-二硝基苯酚或培养基血清浓度降低的抑制。然而,摄入的(125)I-HSA的加工过程会被低温可逆性抑制。脉冲处理的巨噬细胞排泄的三氯乙酸可溶性放射性物质被鉴定为单碘酪氨酸。