Akasaki K, Michihara A, Fukuzawa M, Kinoshita H, Tsuji H
Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima.
J Biochem. 1994 Sep;116(3):670-6.
We studied the endocytic transport of an 85-kDa lysosomal membrane glycoprotein (LGP85) from the cell surface to lysosomes in cultured rat hepatocytes. Fab' fragments of a monoclonal antibody against LGP85 (YA30 mAb) were conjugated with horseradish peroxidase (HRP) and then used as probes to monitor the endocytic transport of LGP85 from the plasma membrane to lysosomes. Continuous internalization and lysosomal transport of HRP-YA30 mAb Fab' occurred in the hepatic cells, resulting in its accumulation in the dense lysosomal fraction obtained from the cells on Percoll density centrifugation. The endocytic transport of HRP-YA30 mAb continued in the presence of the protein synthesis inhibitor, cycloheximide, indicating that LGP85 is cycled between the cell surface and lysosomes or endosomes, like other lysosomal membrane glycoproteins, lamp-1 and lamp-2, as reported previously [Akasaki et al. (1993) J. Biochem. 114, 598-604]. The half times (t1/2) of internalization and lysosomal transport of LGP85 were 32 min and 2.0 h, respectively. The kinetics of endocytic transport for LGP85 are very similar to those of lamp-1 and lamp-2. LGP85 possesses a short cytoplasmic tail whose amino acid sequence is quite different from those of lamp-1 and lamp-2. Therefore, these results suggested that continuous internalization from the cell surface and lysosomal transport of of endogenous LGP85 occur through a mechanism that can recognize this novel amino acid sequence, probably a Leu-Ile-containing motif, in normal hepatic cells of rat.
我们研究了培养的大鼠肝细胞中85 kDa溶酶体膜糖蛋白(LGP85)从细胞表面到溶酶体的内吞运输。抗LGP85单克隆抗体(YA30 mAb)的Fab'片段与辣根过氧化物酶(HRP)偶联,然后用作探针监测LGP85从质膜到溶酶体的内吞运输。HRP-YA30 mAb Fab'在肝细胞中持续内化并向溶酶体运输,导致其在经Percoll密度离心从细胞中获得的致密溶酶体组分中积累。在蛋白质合成抑制剂环己酰亚胺存在的情况下,HRP-YA30 mAb的内吞运输仍在继续,这表明LGP85像其他溶酶体膜糖蛋白lamp-1和lamp-2一样,在细胞表面与溶酶体或内体之间循环,如先前报道 [赤崎等人(1993年)《生物化学杂志》114卷,598 - 604页]。LGP85内化和向溶酶体运输的半衰期(t1/2)分别为32分钟和2.0小时。LGP85的内吞运输动力学与lamp-1和lamp-2非常相似。LGP85具有短的细胞质尾巴,其氨基酸序列与lamp-1和lamp-2的氨基酸序列有很大不同。因此,这些结果表明,在大鼠正常肝细胞中,内源性LGP85从细胞表面的持续内化和向溶酶体的运输是通过一种能够识别这种新氨基酸序列(可能是含亮氨酸 - 异亮氨酸的基序)的机制发生的。