Akasaki K, Michihara A, Fujiwara Y, Mibuka K, Tsuji H
Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima.
J Biochem. 1996 Dec;120(6):1088-94. doi: 10.1093/oxfordjournals.jbchem.a021526.
Lysosomal membranes contain two highly glycosylated proteins, designated as lamp-1 and lamp-2, as major components. Lamp-1 and lamp-2 are similar to each other in the protein structure. Here, we investigated the biosynthetic transport of lamp-2 through the endocytic vacuoles in cultured rat hepatocytes in comparison with that of lamp-1, which has previously been studied [Akasaki et al. (1995) Exp. Cell Res. 220, 464-473]. Newly synthesized lamp-2 (NS-lamp-2) was transported to the trans-Golgi from rough endoplasmic reticulum with a half time (t1/2) of 32 min, more slowly than NS-lamp-1 (t1/2 = 13 min). After leaving the trans-Golgi, NS-lamp-2 is transferred to at least three compartments; the cell surface (t1/2 = 47 min), cell peripheral early endosomes (t1/2 = 38 min) and perinuclear late endosomes (t1/2 = 48 min). NS-lamp-2 transported to any compartment is delivered finally to lysosomes (t1/2 = 90 min). A significant fraction of NS-lamp-2 (45% of the total) was transported from the trans-Golgi to early endosomes, and then delivered to dense lysosomes via perinuclear late endosomes, whereas a major portion of NS-lamp-1 follows an intracellular route to late endosomes without passing through the cell periphery. NS-lamp-2 leaves the cell peripheral region more rapidly than NS-lamp-1. The kinetic and quantitative data for biosynthetic transport of NS-lamp-2 to early endosomes and the cell surface indicate that NS-lamp-2 may be transported first to early endosomes, from which a small portion of it (approximately 3.5% of the total) moves to the plasma membrane via a recycling system. In contrast, a small fraction of NS-lamp-1 is transported to the plasma membrane directly from the trans-Golgi, since NS-lamp-1 is delivered to the plasma membrane and early endosomes with almost the same half times.
溶酶体膜含有两种高度糖基化的蛋白质,即lamp - 1和lamp - 2,作为主要成分。Lamp - 1和lamp - 2在蛋白质结构上彼此相似。在此,我们研究了lamp - 2在培养的大鼠肝细胞中通过内吞泡的生物合成运输,并与之前已研究过的lamp - 1进行了比较[Akasaki等人(1995年)。《实验细胞研究》220,464 - 473]。新合成的lamp - 2(NS - lamp - 2)从粗面内质网运输到反式高尔基体,半衰期(t1/2)为32分钟,比NS - lamp - 1(t1/2 = 13分钟)慢。离开反式高尔基体后,NS - lamp - 2被转移到至少三个区室;细胞表面(t1/2 = 47分钟)、细胞周边早期内体(t1/2 = 38分钟)和核周晚期内体(t1/2 = 48分钟)。运输到任何区室的NS - lamp - 2最终都被递送至溶酶体(t1/2 = 90分钟)。相当一部分NS - lamp - 2(占总量的45%)从反式高尔基体运输到早期内体,然后通过核周晚期内体递送至致密溶酶体,而NS - lamp - 1的主要部分则沿着细胞内途径运输到晚期内体,不经过细胞周边。NS - lamp - 2比NS - lamp - 1更快地离开细胞周边区域。NS - lamp - 2向早期内体和细胞表面生物合成运输的动力学和定量数据表明,NS - lamp - 2可能首先运输到早期内体,其中一小部分(约占总量的3.5%)通过回收系统移动到质膜。相比之下,一小部分NS - lamp - 1直接从反式高尔基体运输到质膜,因为NS - lamp - 1以几乎相同的半衰期被递送至质膜和早期内体。