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核仁异常——核仁前核糖体组装缺陷——见于骨髓增生异常综合征(MDS)的环形铁粒幼细胞性难治性贫血(RARS)中的环形铁粒幼细胞。一项电子显微镜研究。

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.

作者信息

Smetana K, Cermák J, Jirásková I, Malasková V

机构信息

Institute of Haematology and Blood Transfusion, Haematology Clinic, Institute of Medical Postgraduate Studies, Prague, Czech Republic.

出版信息

Sb Lek. 2003;104(2):199-207.

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.

摘要

通过透射电子显微镜对骨髓增生异常综合征(MDS)中伴有环形铁粒幼细胞的难治性贫血(RARS)患者的环形铁粒幼细胞进行研究,以获取更多关于这些异常成红细胞中核仁结构组织的信息。为了对照电子显微镜观察结果,还通过两种广泛使用的细胞化学方法对成红细胞中的核仁进行可视化,以显示RNA和AgNOR蛋白。与先前描述的“正常”成红细胞中核仁的超微结构不同,MDS的RARS中环形成红细胞的核仁经常表现为含致密核糖核酸(RNA)的颗粒成分发生率降低或缺乏。由于含致密RNA的颗粒成分代表前核糖体,因此MDS的RARS中的此类铁粒幼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,在环形铁粒幼细胞的早期发育阶段,如早幼红细胞中未发现前核糖体组装的改变。此外,少数环形铁粒幼细胞的晚期或终末期核仁也未表现出这种核仁异常,从而证实了这些细胞在结构和功能上的巨大变异性。成红细胞晚期和终末期核仁中含RNA结构的缺陷与光学显微镜细胞化学结果一致,光学显微镜细胞化学结果显示,RNA染色标本中的微核仁发生率明显低于AgNOR(银染核仁组织区)蛋白染色标本。

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