Thiry M, Scheer U, Goessens G
Institut d'Histologie, Université de Liège, Belgium.
Eur J Cell Biol. 1988 Dec;47(2):346-57.
In order to investigate the DNA localization within Ehrlich tumor cell nucleoli during mitosis, two recent immunocytochemical methods using either an anti-DNA or an anti-bromodeoxyuridine (BrdU) monoclonal antibody have been applied. In both cases, the immunogold labeling has been performed on ultrathin sections of cells embedded either in Lowicryl K4M or in Epon, respectively. Identical results are observed with both immunocytochemical approaches. In the interphase nucleolus, besides the labeling of the perinucleolar chromatin shell and of its intranucleolar invaginations which penetrate into the nucleolar body and often terminate at the fibrillar centers, a few gold particles are also preferentially found towards the peripheral region of the fibrillar centers. In contrast, the dense fibrillar component and the granular component are never labeled. During mitosis, the fibrillar centers persist at the chromosomal nucleolus organizing regions (NOR's) and can be selectively stained by the silver method. However, these metaphase fibrillar centers are no longer decorated by the DNA- or BrdU antibodies. These results indicate that until the end of prophase, rRNA genes are present inside the fibrillar center material, disappear during metaphase and reappear in reconstituting nucleoli during telophase. Thus, fibrillar centers appear to represent structures sui generis, which are populated by rRNA genes only when the nucleolus is functionally active. In segregated nucleoli after actinomycin D treatment, the DNA labeling is exclusively restricted to the perinucleolar chromatin blocks. These findings also suggest that the DNA content of the fibrillar center material varies according to the rRNA transcription level of the cells. The results are discussed in the light of the present knowledge of the functional organization of the nucleolus.
为了研究有丝分裂期间艾氏瘤细胞核仁内的DNA定位,应用了两种最近的免疫细胞化学方法,分别使用抗DNA或抗溴脱氧尿苷(BrdU)单克隆抗体。在这两种情况下,免疫金标记分别在包埋于Lowicryl K4M或Epon中的细胞超薄切片上进行。两种免疫细胞化学方法都观察到了相同的结果。在间期核仁中,除了核仁周围染色质壳及其伸入核仁体并常常在纤维中心终止的核仁内陷的标记外,还优先在纤维中心的周边区域发现一些金颗粒。相反,致密纤维成分和颗粒成分从未被标记。在有丝分裂期间,纤维中心持续存在于染色体核仁组织区(NOR),并且可以通过银染法进行选择性染色。然而,这些中期纤维中心不再被DNA或BrdU抗体标记。这些结果表明,直到前期结束,rRNA基因都存在于纤维中心物质内部,在中期消失,并在末期重新形成核仁时再次出现。因此,纤维中心似乎代表一种特殊的结构,仅在核仁功能活跃时才含有rRNA基因。在放线菌素D处理后的分离核仁中,DNA标记仅局限于核仁周围的染色质块。这些发现还表明,纤维中心物质的DNA含量根据细胞的rRNA转录水平而变化。根据目前关于核仁功能组织的知识对结果进行了讨论。