Mirre C, Knibiehler B
J Cell Sci. 1982 Jun;55:247-59. doi: 10.1242/jcs.55.1.247.
In mouse testis, the diploid Sertoli cell displays one large nucleolus flanked symmetrically by two heterochromatic masses. The hybridization in situ with [3H]rRNA confirmed that the ribosomal cistrons are localized with in the central nucleolar mass. At the ultrastructural level this nucleolar mass appears to be reticulated and contains numerous fibrillar centres. These fibrillar centres are surrounded and interconnected by an electron-opaque fibrillar network, which constitutes the reticulated nucleolonema of the nucleolus. Ag--NOR staining reveals the presence of the argyrophilic proteins associated with active nucleolus-organizing regions (NORs) within both the fibrillar centres and the electron-opaque fibrillar component. Autoradiographic studies after [3H]uridine incorporation show that ribosomal DNA transcription only takes place in this dense fibrillar component. Three-dimensional reconstruction of four Sertoli cell nucleoli after serial sectioning reveals that the size and number of the fibrillar centers are very variable from one cell to another (26, 35, 38 an 41 fibrillar centres). The analysis of the volume occupied by the fibrillar centres as compared to the whole nucleolar volume demonstrates that the larger the nucleolus, the more fibrillar centres it contains, but also the more numerous the fibrillar centres, the larger their total volume. While in each case the number of the NORs is virtually the same, i.e. ten. In the light of these results we concluded that, at least in reticulated nucleoli, there is no numerical relationship between the number of fibrillar centres and the number of NORs, and that the fibrillar centers cannot be considered only as the nucleolar counterparts of the NORs. Moreover, the increasing number of fibrillar centres from the smallest nucleolus to the largest one is difficult to explain by the previously postulated hypothesis of a reserve of inactive rDNA packaged in the fibrillar centers. These data led us to reconsider the role of the fibrillar centres in the transcriptional activity of reticulated nucleoli.
在小鼠睾丸中,二倍体支持细胞显示出一个大核仁,其两侧对称地分布着两个异染色质块。用[3H]rRNA进行原位杂交证实,核糖体顺反子位于中央核仁块内。在超微结构水平上,这个核仁块似乎呈网状,包含许多纤维中心。这些纤维中心被一个电子致密的纤维网络包围并相互连接,该网络构成了核仁的网状核仁丝。银染核仁组织区(Ag-NOR)染色显示,在纤维中心和电子致密的纤维成分中都存在与活跃核仁组织区(NORs)相关的嗜银蛋白。[3H]尿苷掺入后的放射自显影研究表明,核糖体DNA转录仅发生在这个致密的纤维成分中。对四个支持细胞核仁进行连续切片后的三维重建显示,纤维中心的大小和数量在不同细胞之间差异很大(分别有26、35、38和41个纤维中心)。将纤维中心所占体积与整个核仁体积进行比较分析表明,核仁越大,其包含的纤维中心越多,而且纤维中心数量越多,其总体积也越大。而在每种情况下,NORs的数量实际上是相同的,即十个。根据这些结果,我们得出结论,至少在网状核仁中,纤维中心的数量与NORs的数量之间不存在数字关系,并且不能仅将纤维中心视为NORs的核仁对应物。此外,按照先前假设的存在包装在纤维中心的无活性rDNA储备的假说,很难解释从最小的核仁到最大的核仁纤维中心数量不断增加的现象。这些数据促使我们重新考虑纤维中心在网状核仁转录活性中的作用。