Nebiyyeh Kamaci, Tuba Emnacar, Nihal Karakas, Gulsum Arikan, Ken Tsutsui, Sevim Isik
{"title":"Selective silencing of DNA topoisomerase IIβ in human mesenchymal stem cells by siRNAs (small interfering RNAs)","authors":"Nebiyyeh Kamaci, Tuba Emnacar, Nihal Karakas, Gulsum Arikan, Ken Tsutsui, Sevim Isik","doi":"10.1042/CBR20110003","DOIUrl":null,"url":null,"abstract":"<p>hMSCs (human mesenchymal stem cells) express two isoforms of DNA topo II (topoisomerase II). Although both isoforms have the same catalytic activity, they are specialized for different functions in the cell: while topo IIα is essential for chromosome segregation in mitotic cells, topo IIβ is involved in more specific cellular functions. A number of inhibitors are available that inhibit the catalytic activity of both topo II isoforms. However, in order to investigate the isoform-specific inhibition of these two enzymes, it is necessary to use other techniques such as siRNA (small interfering RNA) interference to selectively silence either one of the isoforms individually. Depending on the lipid charge densities and protein varieties of the cell membrane, previous studies have demonstrated that transfection efficiencies of siRNAs to hMSCs are very low. In the study reported here, we demonstrate the use of Lipofectamine RNAiMAX as an efficient transfection reagent to introduce siRNAs into human mesenchymal stem cells with significantly great efficiency to silence topo IIβ selectively. A high level of transfection efficiency (80%) was achieved by using unlabelled topo IIβ-specific siRNA oligos. Specifically, it was confirmed repeatedly that green labelled siRNAs interfere with the transfection of siRNAs. The reagent induced minimal cytotoxicity (3.5–4.5%), and cell viability of the transfected hMSCs decreased 20–30% compared with untreated cells, depending on the concentration of the reagent.</p>","PeriodicalId":75683,"journal":{"name":"Cell biology international reports","volume":"18 1","pages":"15-21"},"PeriodicalIF":0.0000,"publicationDate":"2013-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1042/CBR20110003","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell biology international reports","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1042/CBR20110003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
Abstract
hMSCs (human mesenchymal stem cells) express two isoforms of DNA topo II (topoisomerase II). Although both isoforms have the same catalytic activity, they are specialized for different functions in the cell: while topo IIα is essential for chromosome segregation in mitotic cells, topo IIβ is involved in more specific cellular functions. A number of inhibitors are available that inhibit the catalytic activity of both topo II isoforms. However, in order to investigate the isoform-specific inhibition of these two enzymes, it is necessary to use other techniques such as siRNA (small interfering RNA) interference to selectively silence either one of the isoforms individually. Depending on the lipid charge densities and protein varieties of the cell membrane, previous studies have demonstrated that transfection efficiencies of siRNAs to hMSCs are very low. In the study reported here, we demonstrate the use of Lipofectamine RNAiMAX as an efficient transfection reagent to introduce siRNAs into human mesenchymal stem cells with significantly great efficiency to silence topo IIβ selectively. A high level of transfection efficiency (80%) was achieved by using unlabelled topo IIβ-specific siRNA oligos. Specifically, it was confirmed repeatedly that green labelled siRNAs interfere with the transfection of siRNAs. The reagent induced minimal cytotoxicity (3.5–4.5%), and cell viability of the transfected hMSCs decreased 20–30% compared with untreated cells, depending on the concentration of the reagent.
hMSCs(人间充质干细胞)表达两种DNA拓扑异构酶(topo II)的同工异构体。尽管这两种同工异构体具有相同的催化活性,但它们在细胞中具有不同的功能:topo IIα对于有丝分裂细胞中的染色体分离至关重要,而topo IIβ则参与更特定的细胞功能。许多抑制剂可以抑制拓扑II同工异构体的催化活性。然而,为了研究这两种酶的异构体特异性抑制,有必要使用其他技术,如siRNA(小干扰RNA)干扰来选择性地单独沉默其中一种异构体。根据细胞膜的脂质电荷密度和蛋白质种类,先前的研究表明sirna转染hMSCs的效率非常低。在这里报道的研究中,我们证明了使用Lipofectamine RNAiMAX作为一种有效的转染试剂,将sirna引入人间充质干细胞,具有显著的选择性沉默topo i β的效率。通过使用未标记的topo i β特异性siRNA寡核苷酸,实现了高水平的转染效率(80%)。具体地说,绿色标记的sinas干扰sinas的转染。该试剂诱导的细胞毒性最小(3.5-4.5%),转染的hMSCs的细胞活力与未处理的细胞相比下降了20-30%,这取决于试剂的浓度。