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无菌培养的溶组织内阿米巴HM1:IMSS克隆A中DNA含量的异质性及细胞周期基因的表达

Heterogeneity of DNA content and expression of cell cycle genes in axenically growing Entamoeba histolytica HM1:IMSS clone A.

作者信息

Gangopadhyay S S, Ray S S, Kennady K, Pande G, Lohia A

机构信息

Department of Biochemistry, Bose Institute, Calcutta, India.

出版信息

Mol Biochem Parasitol. 1997 Dec 1;90(1):9-20. doi: 10.1016/s0166-6851(97)00156-4.

Abstract

The cell division cycle of Entamoeba histolytica was studied using multi-parametric flow cytometry in asynchronous and partially synchronised cells. Dynamic changes in the DNA synthesis and DNA content of axenically growing trophozoites were observed by using 5-bromo-2'-deoxyuridine (BrdU) uptake and DNA specific fluorochromes. It was observed that DNA synthesis in these cells continues beyond the typical S-phase stop point when DNA duplication is complete. Asynchronously growing E. histolytica cells could be synchronised by serum starvation followed by serum re-addition. BrdU incorporation in synchronised cells showed that cell synchrony is maintained for at least one generation time, in which the G1 phase lasts for 2-3 h and the S-phase lasts for 5-6 h. Analysis of our results revealed that E. histolytica trophozoites, growing in axenic medium, are made up of a heterogenous population of euploid and polyploid cells. The number of polyploid cells increases with age of the cells in culture. Expression of putative cell cycle and signal transduction markers was studied using specific antibodies and changes in their expression levels have been correlated with changes in the DNA content. Based upon our results we could identify G1, S and G2 phases of the cell cycle of E. histolytica and also predict the mechanism underlying the generation of polyploidy in these cells, which may have significant effects on its biology and pathogenesis.

摘要

利用多参数流式细胞术对溶组织内阿米巴在非同步化和部分同步化细胞中的细胞分裂周期进行了研究。通过使用5-溴-2'-脱氧尿苷(BrdU)摄取和DNA特异性荧光染料,观察了在无菌培养的滋养体中DNA合成和DNA含量的动态变化。结果发现,这些细胞中的DNA合成在DNA复制完成后仍会持续超过典型的S期停止点。非同步生长的溶组织内阿米巴细胞可通过血清饥饿后再添加血清来实现同步化。同步化细胞中BrdU的掺入表明细胞同步性至少可维持一个世代时间,其中G1期持续2 - 3小时,S期持续5 - 6小时。对我们结果的分析表明,在无菌培养基中生长的溶组织内阿米巴滋养体由整倍体和多倍体细胞组成的异质群体构成。多倍体细胞的数量随着培养细胞年龄的增长而增加。使用特异性抗体研究了假定的细胞周期和信号转导标志物的表达,并且它们表达水平的变化已与DNA含量的变化相关联。基于我们的结果,我们能够确定溶组织内阿米巴细胞周期的G1、S和G2期,还能预测这些细胞中多倍体产生的潜在机制,这可能对其生物学和发病机制产生重大影响。

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