Stepiński Dariusz
Department of Cytophysiology, University of Lódź, Poland.
Folia Histochem Cytobiol. 2004;42(1):57-61.
Ultrastructural and autoradiographic studies of nucleoli in soybean root meristematic cells in seedlings: (1) grown for 3 days at 25 degrees C (control), (2) grown for three days at 25 degrees C and for 4 days at 10 degrees C, and (3) grown as in (2) and recovered for 1 day at 25 degrees C were carried out. Control nucleoli had dense structure and a few small nucleolar vacuoles. Chilled plant nucleoli had less dense structure and no vacuoles. Nucleoli of plants recovered at 25 degrees C had big nucleolar vacuoles. In autoradiograms of squashed preparations, the labeling of nucleoli and cytoplasm after 20-min incubation in 3H-uridine was 5- and 6-fold stronger, respectively, in control than in chilled roots. Following recovery, the labeling of nucleoli and cytoplasm was much stronger than after chilling or even than in control roots. After 80-min postincubation in non-radioactive medium, average labeling of particular areas of cells was the highest in recovered plants which indicated intensification of rRNA synthesis, maturation and transport into cytoplasm resulting from the resumption of optimal conditions which was correlated with the appearance of big nucleolar vacuoles. In autoradiograms of semi-thin sections from roots of seedlings chilled for 4 days then recovered and incubated for 20 min in 3H-uridine, practically only extravacuolar parts of nucleoli were labeled. After 80-min postincubation, the labeling of nucleolar vacuoles was observed. Thus, during postincubation the labeled molecules were translocated from the nucleolar periphery into nucleolar vacuoles in cells where intensive transport of these molecules to the cytoplasm takes place. On the basis of these results, a hypothesis has been put forward that nucleolar vacuoles may be involved in the intensification of pre-ribosome transport outside nucleolus.
(1)在25℃下培养3天(对照);(2)在25℃下培养3天,然后在10℃下培养4天;(3)如(2)所述培养并在25℃下恢复1天。对照核仁结构致密,有一些小的核仁液泡。受冷植物的核仁结构较疏松,没有液泡。在25℃恢复的植物核仁有大的核仁液泡。在压片制备的放射自显影片中,用3H-尿苷孵育20分钟后,对照根中核仁和细胞质的标记分别比受冷根强5倍和6倍。恢复后,核仁和细胞质的标记比受冷后甚至比对照根更强。在非放射性培养基中孵育80分钟后,恢复植物中细胞特定区域的平均标记最高,这表明由于最佳条件的恢复,rRNA合成、成熟和向细胞质运输增强,这与大核仁液泡的出现相关。在对幼苗根进行4天冷处理然后恢复并在3H-尿苷中孵育20分钟的半薄切片的放射自显影片中,实际上只有核仁的液泡外部分被标记。孵育80分钟后,观察到核仁液泡有标记。因此,在孵育后,标记分子从核仁周边转移到细胞中的核仁液泡中,在这些细胞中这些分子向细胞质进行大量运输。基于这些结果,提出了一个假说,即核仁液泡可能参与核仁外前核糖体运输的增强。