el-Alfy M, Leblond C P
Department of Anatomy, McGill University, Montreal, Quebec, Canada.
Am J Anat. 1989 Sep;186(1):69-84. doi: 10.1002/aja.1001860106.
The phases of mitosis were examined in the columnar cells at the base of duodenal crypts in adult male mice given an intravenous injection of 3H-thymidine and sacrificed 20 min later. The duodenum was fixed by immersion into glutaraldehyde-formaldehyde, and the cells were examined in the electron microscope, with or without processing for radioautography. Interphase nuclei are characterized by the distribution of chromatin; aside from the cortical chromatin spread along nuclear envelope and nucleolus, there are chromatin accumulations that belong mainly in two different classes: 1) numerous chromatin "specks" ranging in size from about 5 to 70 nm and averaging 47 nm; 2) a few roughly circular or elongated chromatin "packets" measuring from 70 to 230 nm. Early prophase nuclei differ mainly by a large increase in the number of chromatin packets to 20-30 or more per nuclear profile; their average diameter is 128 nm. During mid-prophase, the chromatin packets enlarge gradually to an average 221 nm diameter. Between mid- and late prophase, there is a further increase in diameter to 679 nm. At metaphase, the packets take on the appearance of mature chromosomes, and their diameter increases to 767 nm. At anaphase, daughter chromosomes migrate to each pole, where they fuse into a compact chromatin mass. At telophase, nucleoplasmic areas progressively enlarge within the chromatin mass and separate strands of chromatin, which gradually become segmented into chromatin clumps. Counts of mitotic cells show a high proportion of prophase and telophase nuclei. Calculation from the counts yields the duration of the phases, that is, 5.6, 0.2, 0.1, and 1.6 hr, respectively, for pro-, meta-, ana-, and telophase. Finally, radioautography 20 min after 3H-thymidine injection shows labeling in 54% of the interphase nuclei, 85% of early prophase nuclei, and 73% of mid-prophase nuclei, while there is no label in late prophase, metaphase, anaphase and telophase nuclei. In confirmation of previous light microscopic work, the S stage of the cycle begins when a cell is in interphase and continues through the early prophase and part of mid-prophase. Moreover, the main sites of DNA synthesis are the chromatin specks during interphase and the cortical chromatin during early and mid-prophase. The chromosome condensation taking place in the meantime may be separated into two main steps: 1) a slow, moderate condensation of the chromatin packets during early and mid-prophase and 2) a rapid, pronounced one during late prophase and prometaphase when the packets become chromosomes.
给成年雄性小鼠静脉注射³H - 胸腺嘧啶核苷,20分钟后处死,检查十二指肠隐窝底部柱状细胞的有丝分裂阶段。将十二指肠浸入戊二醛 - 甲醛中固定,然后在电子显微镜下检查细胞,部分细胞进行放射自显影处理,部分不进行。间期核的特征在于染色质的分布;除了沿核膜和核仁分布的皮质染色质外,还有主要属于两类的染色质聚集:1)许多大小约为5至70纳米、平均为47纳米的染色质“斑点”;2)一些大小为70至230纳米的大致圆形或细长的染色质“小体”。早期前期核的主要区别在于每个核轮廓中染色质小体的数量大幅增加至20 - 30个或更多;其平均直径为128纳米。在中期前期,染色质小体逐渐增大至平均直径221纳米。在中期前期和后期前期之间,直径进一步增加至679纳米。在中期,小体呈现成熟染色体的外观,其直径增加至767纳米。在后期,子染色体迁移到每个极,在那里它们融合成紧密的染色质团块。在末期,核质区域在染色质团块内逐渐扩大,并分离出染色质链,这些染色质链逐渐分成染色质团块。有丝分裂细胞计数显示前期和末期核的比例很高。根据计数计算得出各阶段的持续时间,即前期、中期、后期和末期分别为5.6、0.2、0.1和1.6小时。最后,注射³H - 胸腺嘧啶核苷20分钟后的放射自显影显示,54%的间期核、85%的早期前期核和73%的中期前期核有标记,而后期前期、中期、后期和末期核无标记。证实先前的光学显微镜研究结果,细胞周期的S期始于细胞处于间期时,并持续到早期前期和部分中期前期。此外,DNA合成的主要位点在间期是染色质斑点,在早期和中期前期是皮质染色质。与此同时发生的染色体凝聚可分为两个主要步骤:1)在早期和中期前期染色质小体的缓慢、适度凝聚;2)在后期前期和前中期染色质小体变成染色体时的快速、明显凝聚。