Demin S Iu
Tsitologiia. 1997;39(2-3):253-63.
A method of a stage by stage dismantling of the cell nucleus by a 0.5-5 min resuspending cells in physiological media containing 0.05 and 0.5% of non-ionic detergent Triton X-100 is first described. Depending on the detergent concentration and cell incubation time a suspension was obtained consisting of either practically undamaged nuclei with removed envelopes, cytoplasm-free mitotic figures and isolated envelopes gradually spreading interphase chromatin associated with nucleoplasm proteins. The article describes a technique to make from such a suspension preparations of spread and flattened derivatives of nucleus and mitotic chromosomes to use for optical microscopic research. This method allows to reveal perichromatin components of the nucleus and mitotic chromosome to study structure of chromonemic net and nucleoli of diploid nuclei of human leucocytes and non-polytenic nuclei of chironomus epitheliocytes and the discoidal structure of polynemic (low-polytenic) chromosomes from the midgut epithelium cells of chironomus larvae. An attempt was made to use the obtained preparations of flattened unenveloped nuclei in order to distinguish between human leucocytes according to the structure of their chromonemic net and silver-stained nucleolus, and to find out the manner of impregnation of argyrophilic nucleoplasm proteins. The partially isolated chironomus polynemic chromosomes have morphological manifestations of unproportional endoreduplication, local compactization of chromomers and physical association between a nucleolus and numerous of distant chromosome loci. We failed, however, to find any homology in the band pattern of such polynemic chromosomes and polytenic chromosomes of larval salivary gland cells. Individuality of chromosomes in polynemic nuclei was not so obvious due to a developed network of intra- and interchromosomal ectopic contacts. The discussion touches upon the mechanisms of isolation of nuclear envelopes and ways to restore the original shape of the unenveloped nucleus in the used hydrodynamic system with fading detergent activity. Prospects are mapped out to use this technique in the structural studies of interphase nuclei and mitotic and polynemic chromosomes.
首次描述了一种通过在含有0.05%和0.5%非离子去污剂Triton X - 100的生理介质中重悬细胞0.5 - 5分钟,逐步拆解细胞核的方法。根据去污剂浓度和细胞孵育时间,获得了一种悬浮液,其由几乎未受损的、包膜已去除的细胞核、无细胞质的有丝分裂图像以及逐渐伸展的、与核质蛋白相关的间期染色质的分离包膜组成。本文描述了一种从这种悬浮液制备细胞核和有丝分裂染色体的伸展和平展衍生物用于光学显微镜研究的技术。该方法能够揭示细胞核和有丝分裂染色体的染色质周边成分,以研究人类白细胞二倍体细胞核以及摇蚊上皮细胞非多线细胞核的染色线网和核仁结构,以及摇蚊幼虫中肠上皮细胞多线(低多线)染色体的盘状结构。尝试使用所获得的伸展的无包膜细胞核制剂,根据其染色线网和银染核仁的结构来区分人类白细胞,并找出嗜银核质蛋白的浸染方式。部分分离的摇蚊多线染色体具有不成比例的核内复制、染色粒局部致密化以及核仁与众多远距离染色体位点之间物理关联的形态学表现。然而,我们未能在这种多线染色体与幼虫唾液腺细胞的多线染色体的带型中发现任何同源性。由于染色体间和染色体内异位接触网络发达,多线细胞核中染色体的个体性并不那么明显。讨论涉及核包膜的分离机制以及在去污剂活性逐渐消失的所用流体动力学系统中恢复无包膜细胞核原始形状 的方法。规划了将该技术用于间期细胞核以及有丝分裂和多线染色体结构研究的前景。