Zybina Eugenia V, Zybina Tatiana G
Institute of Cytology, Russian Academy of Sciences, St Petersburg, Russia.
Micron. 2008 Jul;39(5):593-606. doi: 10.1016/j.micron.2007.05.006. Epub 2007 May 31.
An increased activity of membranes of the nuclear envelope (NE) was observed electron microscopically in the trophoblast cells of the rat placenta. The activity of the membranes was manifested as formation of various NE derivatives, such as the annulate lamellae (AL), the intranuclear tubules, and the concentric membranous structures. At the period of terminal differentiation of the secondary giant trophoblast cells (SGTC) the NE derivatives play active role in subdivision of the initial highly polyploid nuclei into the numerous low-ploidy fragments. (3)H-thymidine labeling showed that attenuation of the DNA replication precedes the nuclear fragmentation. In the course of the nuclear fragmentation the narrow deep NE invaginations subdivide the nucleus into the separate lobes that subsequently are detached from the initial nucleus. By the beginning of the fragmentation, the accumulated membranous structures, i.e. the intranuclear AL, tubules, clusters of pore complexes, etc., seem to be the source of the reserve material that is necessary for formation of the great amount of the NE membranes of the newly formed nuclear fragments. Thus, the intranuclear membranous structures that seem to increase the active surface of the growing endopolyploid nucleus at the earlier stage of differentiation then take part in genome isolation that results in formation of a multinucleate cell with diploid and low-polyploid nuclei. The outer NE membrane of the initial nucleus plays an active role in compartmentalization of cytoplasmic areas around the nuclear fragments within the giant polykaryocyte. Apart from the membranous structures the bundles of intermediate filaments (IF) located in the cytoplasm perinuclear zones seem to participate in the nuclear fragmentation. These processes are likely to provide formation of the giant polykaryocytes incapable for further proliferation.
在大鼠胎盘的滋养层细胞中,通过电子显微镜观察到核膜(NE)的膜活性增加。膜的活性表现为形成各种核膜衍生物,如环状片层(AL)、核内小管和同心膜结构。在次级巨大滋养层细胞(SGTC)终末分化期间,核膜衍生物在将初始高度多倍体核细分为众多低倍体片段中发挥积极作用。(3)H-胸腺嘧啶核苷标记显示DNA复制的减弱先于核碎片化。在核碎片化过程中,狭窄而深的核膜内陷将核细分为单独的叶,这些叶随后从初始核上分离。到碎片化开始时,积累的膜结构,即核内的AL、小管、孔复合体簇等,似乎是新形成的核片段大量核膜形成所需储备物质的来源。因此,核内膜结构在分化早期似乎增加了不断增长的内多倍体核的活性表面,然后参与基因组隔离,导致形成具有二倍体和低倍体核的多核细胞。初始核的外核膜在巨大多核细胞内核片段周围的细胞质区域分隔中发挥积极作用。除了膜结构外,位于核周细胞质区域的中间丝(IF)束似乎也参与了核碎片化。这些过程可能有助于形成无法进一步增殖的巨大多核细胞。