Tilney L G, Tilney M S, Guild G M
Department of Biology, University of Pennsylvania, Philadelphia, 19104, USA.
J Cell Biol. 1996 Apr;133(1):61-74. doi: 10.1083/jcb.133.1.61.
Growing the intracellular bridges that connect nurse cells with each o ther and to the developing oocyte is vital for egg development. These ring canals increase from 0.5 microns in diameter at stage 2 to 10 microns in diameter at stage 11. Thin sections cut horizontally as you would cut a bagel, show that there is a layer of circumferentially oriented actin filaments attached to the plasma membrane at the periphery of each canal. By decoration with subfragment 1 of myosin we find actin filaments of mixed polarities in the ring such as found in the "contractile ring" formed during cytokinesis. In vertical sections through the canal the actin filaments appear as dense dots. At stage 2 there are 82 actin filaments in the ring, by stage 6 there are 717 and by stage 10 there are 726. Taking into account the diameter, this indicates that there is 170 microns of actin filaments/canal at stage 2 (pi x 0.5 microns x 82), 14,000 microns at stage 9 and approximately 23,000 microns at stage 11 or one inch of actin filament! The density of actin filaments remains unchanged throughout development. What is particularly striking is that by stages 4-5, the ring of actin filaments has achieved its maximum thickness, even though the diameter has not yet increased significantly. Thereafter, the diameter increases. Throughout development, stages 2-11, the canal length also increases. Although the density (number of actin filaments/micron2) through a canal remains constant from stage 5 on, the actin filaments appear as a net of interconnected bundles. Further information on this net of bundles comes from studying mutant animals that lack kelch, a protein located in the ring canal that has homology to the actin binding protein, scruin. In this mutant, the actin filaments form normally but individual bundles that comprise the fibers of the net are not bound tightly together. Some bundles enter into the ring canal lumen but do not completely occlude the lumen. all these observations lay the groundwork for our understanding of how a noncontractile ring increases in thickness, diameter, and length during development.
形成连接滋养细胞彼此以及与发育中卵母细胞的细胞内桥对于卵子发育至关重要。这些环管的直径从第2阶段的0.5微米增加到第11阶段的10微米。水平切割的薄片(就像切割百吉饼一样)显示,在每个环管周边的质膜上附着有一层圆周排列的肌动蛋白丝。通过用肌球蛋白亚片段1进行标记,我们发现在环中存在极性混合的肌动蛋白丝,就像在胞质分裂期间形成的“收缩环”中发现的那样。在穿过环管的垂直切片中,肌动蛋白丝呈现为密集的点。在第2阶段,环中有82根肌动蛋白丝,到第6阶段有717根,到第10阶段有726根。考虑到直径,这表明在第2阶段每个环管中有170微米的肌动蛋白丝(π×0.5微米×82),在第9阶段有14,000微米,在第11阶段约有23,000微米,即一英寸长的肌动蛋白丝!肌动蛋白丝的密度在整个发育过程中保持不变。特别引人注目的是,到第4 - 5阶段,尽管直径尚未显著增加,但肌动蛋白丝环已达到其最大厚度。此后,直径增加。在整个第2 - 11阶段的发育过程中,环管长度也增加。虽然从第5阶段开始,穿过环管的密度(每平方微米的肌动蛋白丝数量)保持恒定,但肌动蛋白丝呈现为相互连接的束状网络。关于这个束状网络的更多信息来自对缺乏kelch的突变动物的研究,kelch是一种位于环管中的蛋白质,与肌动蛋白结合蛋白scruin具有同源性。在这种突变体中,肌动蛋白丝正常形成,但构成网络纤维的各个束没有紧密结合在一起。一些束进入环管腔但没有完全阻塞管腔。所有这些观察结果为我们理解非收缩环在发育过程中如何增加厚度、直径和长度奠定了基础。