Gruijters W T M
School of Biological Sciences, The University of Auckland, Private Bag 92091, Auckland, New Zealand.
Cell Biol Int. 2003;27(9):711-7. doi: 10.1016/s1065-6995(03)00140-9.
Gap junction channels are concentrated in specialised plaques of plasma membrane where cells are in close apposition. In this communication evidence is provided showing that these specialised regions of membrane also provide a site for vesicular transfer between cells. Vesicle distribution in eye lenses was found to generally reflect the reported distribution of gap junction membrane plaques. In certain areas of the lens gap junction membrane plaques and vesicles could be seen to form combined, complex structures. Ultrastructure of the vesicle and gap junction membrane plaque complexes was consistent with the vesicles moving through membrane plaques from one lens fibre cell to the next. To investigate whether transport of substances was consistent with intercellular vesicle transfer, transport of various markers was investigated. Time course experiments showing the rate of uptake of various markers into the lens did not show dramatic differences for molecules smaller or larger then gap junction pores formed by connexons. While considered as a primary intercellular transport mechanism in the lens, connexon pores were not the sole agent mediating the observed transport. Other reported mechanisms of intercellular transport in the lens can only account for the movement of relatively small molecules. Vesicular transport may therefore be a major form of transport into the outer lens layers for larger molecules. Implicit in these observations is a new hypothesis for intercellular vesicle movement via gap junction membrane plaques. Intercellular vesicle movement could possibly provide a path for large molecules associated with intact vesicles to be transported into the eye lens tissue.
缝隙连接通道集中在细胞膜的特殊斑块中,细胞在此紧密相邻。本文提供的证据表明,这些特殊的膜区域也为细胞间的囊泡转运提供了一个位点。晶状体中囊泡的分布通常反映了已报道的缝隙连接膜斑块的分布。在晶状体的某些区域,可以看到缝隙连接膜斑块和囊泡形成了组合的复杂结构。囊泡与缝隙连接膜斑块复合物的超微结构与囊泡从一个晶状体纤维细胞穿过膜斑块移动到下一个细胞的情况一致。为了研究物质的转运是否与细胞间囊泡转运一致,对各种标记物的转运进行了研究。显示各种标记物进入晶状体摄取速率的时间进程实验表明,对于小于或大于由连接蛋白形成的缝隙连接孔的分子,摄取速率没有显著差异。虽然缝隙连接孔被认为是晶状体中的主要细胞间转运机制,但它并不是介导观察到的转运的唯一因素。晶状体中其他已报道的细胞间转运机制只能解释相对小分子的移动。因此,囊泡转运可能是较大分子进入晶状体外层的主要转运形式。这些观察结果隐含着一个关于通过缝隙连接膜斑块进行细胞间囊泡移动的新假说。细胞间囊泡移动可能为与完整囊泡相关的大分子进入晶状体组织提供一条途径。