Nucleolar abnormalities--a defect of the nucleolar preribosome assembly--in ringed sideroblasts in refractory anaemia with ringed sideroblasts (RARS) of myelodysplastic syndrome (MDS). An electron microscopic study.

Sbornik lekarsky Pub Date : 2003-01-01
K Smetana, J Cermák, I Jirásková, V Malasková
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Abstract

Ringed sideroblasts were studied by means of transmission electron microscopy in patients suffering from refractory anaemia with ringed sideroblasts (RARS) of myelodysplastic syndrome (MDS) to provide more information on the structural organization of nucleoli in these abnormal erythroblasts. For control of the electron microscopic observations nucleoli in erythroblasts were also visualized by two widely used cytochemical procedures for the demonstration of RNA and AgNOR proteins. In contrast to previously described ultrastructure of nucleoli in "normal" erythroblasts, nucleoli of ringed erythroblasts in RARS of MDS were frequently characterized by a reduced incidence or lack of dense ribonucleic acid (RNA) containing granular components. Since the dense RNA containing granular components represent preribosomes, such sideroblasts in RARS of MDS exhibit a further nucleolar abnormality, which reflects a severe alteration of the nucleolar ribosome assembly in these abnormal cells. On the other hand, the alteration of the preribosome assembly was not noted in early developmental stages of ringed sideroblasts such as proerythroblasts. In addition, nucleoli in advanced or terminal stages of few ringed sideroblasts also did not exhibit such nucleolar abnormality and thus confirm a great structural and functional variability of these cells. The defect of RNA containing structures in nucleoli of advanced and terminal stages of erythroblasts are in a hormony with the light microscopic cytochemistry, which demonstrated a significantly smaller incidence of micronucleoli in specimens stained for RNA than in those stained for AgNOR (silver stained nucleolus organizer region) proteins.

骨髓增生异常综合征(MDS)伴环状铁母细胞难治性贫血(RARS)的环状铁母细胞核仁异常——核仁前核糖体组装的缺陷。电子显微镜研究。
应用透射电镜对骨髓增生异常综合征(MDS)患者的环状铁母细胞(RARS)进行了研究,以进一步了解这些异常红母细胞核仁的结构组织。为了控制电镜观察,还通过两种广泛使用的细胞化学方法来显示红母细胞的核仁,以证明RNA和AgNOR蛋白。与先前描述的“正常”红母细胞核仁的超微结构相反,MDS RARS中环状红母细胞核仁的特征通常是含有颗粒成分的致密核糖核酸(RNA)的发生率降低或缺乏。由于含有颗粒成分的致密RNA代表核糖体前体,MDS的RARS中的这种铁母细胞表现出进一步的核仁异常,这反映了这些异常细胞中核仁核糖体组装的严重改变。另一方面,在环状铁母细胞如原红母细胞的早期发育阶段未注意到前核糖体组装的改变。此外,少数环状铁母细胞的晚期或终末核仁也没有出现这种核仁异常,从而证实了这些细胞在结构和功能上的巨大变异性。红母细胞晚期和末期核仁中含有RNA结构的缺陷与光镜细胞化学是一致的,这表明在RNA染色的标本中微核仁的发生率明显低于AgNOR(银染色核仁组织区)蛋白染色的标本。
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