Docherty P A, Snider M D
Department of Biochemistry, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106.
J Cell Physiol. 1991 Jan;146(1):34-42. doi: 10.1002/jcp.1041460106.
Incubation of cultured cells in hypertonic medium and sodium-free medium have been shown to block transport at two different stages along the endocytic pathway. To determine the effects of these treatments on the exocytic pathway, we studied the transport of the membrane glycoprotein of vesicular stomatitis virus (VSV-G) in cells infected with tsO45 mutant virus. This mutant synthesizes a VSV-G that accumulates in the endoplasmic reticulum (ER) when cells are incubated at 39.5 degrees C. In addition, VSV-G accumulates in the post-ER pre-Golgi compartment when cells are incubated at 15 degrees C and in the trans-Golgi network (TGN) when cells are incubated at 18 degrees C. Upon transfer of cells to 32 degrees C in control medium, VSV-G exits each of these compartments and is transported to the cell surface. Incubation in sodium-free medium at 32 degrees C did not block transport from any of these three compartments. In contrast, incubation in hypertonic medium blocked export from the ER, transport from the pre-Golgi compartment to the Golgi complex, and transport from the TGN to the cell surface. Our results, in combination with previous studies, suggest that hypertonic medium blocks at least five distinct transport steps; the three exocytic steps described here, endocytosis from the cell surface, and transport of cell surface proteins into the Golgi complex. This raises the possibility that vesicular transport in different parts of the cell shares common elements that are inhibited by this treatment.
已证明,将培养细胞置于高渗培养基和无钠培养基中会在沿内吞途径的两个不同阶段阻断转运。为了确定这些处理对胞吐途径的影响,我们研究了水泡性口炎病毒(VSV-G)膜糖蛋白在感染tsO45突变病毒的细胞中的转运情况。这种突变体合成的VSV-G在细胞于39.5摄氏度孵育时会在内质网(ER)中积累。此外,当细胞在15摄氏度孵育时,VSV-G会在ER后的高尔基体前区室中积累,而当细胞在18摄氏度孵育时,会在反式高尔基体网络(TGN)中积累。在对照培养基中将细胞转移至32摄氏度后,VSV-G会从这些区室中的每一个中排出并转运至细胞表面。在32摄氏度的无钠培养基中孵育不会阻断从这三个区室中的任何一个的转运。相比之下,在高渗培养基中孵育会阻断从ER的输出、从高尔基体前区室到高尔基体复合体的转运以及从TGN到细胞表面的转运。我们的结果与先前的研究相结合,表明高渗培养基至少阻断了五个不同的转运步骤;此处描述的三个胞吐步骤、从细胞表面的内吞作用以及细胞表面蛋白向高尔基体复合体的转运。这增加了一种可能性,即细胞不同部位的囊泡转运共享被这种处理抑制的共同元件。