首页> 外文期刊>Cell biology international. >The poly‐cistronic expression of four transcriptional factors (CRX, RAX, NEURO‐D, OTX2) in fibroblasts via retro‐ or lentivirus causes partial reprogramming into photoreceptor cells
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The poly‐cistronic expression of four transcriptional factors (CRX, RAX, NEURO‐D, OTX2) in fibroblasts via retro‐ or lentivirus causes partial reprogramming into photoreceptor cells

机译:通过retro-或慢性病毒在成纤维细胞中的四个转录因子(Crx,rax,neuro-d,Otx2)的多睛分叉表达导致部分重新编程到光感受器细胞中

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Abstract The introduction of four key transcriptional factors (CRX, RAX, NEURO‐D, OTX2) allows the direct differentiation of fibroblasts to retinal photoreceptor cells. This reprogramming was achieved with a combination of mono‐cistronic viruses. Although the combination of mono‐cistronic viruses was useful, a relatively high titer of recombinant viruses was necessary because co‐infections are required. To overcome this issue, we established a poly‐cistronic expression system for direct reprogramming and analyzed the biological characteristics of introduced cells after the exogenous introduction. The coding region of four reprogramming factors and EGFP (CRX, RAX, NEURO‐D, OTX2, and EGFP; CNROE) was inserted into multiple sites of the pMYs‐IP retrovirus or CSII‐CMV lentivirus vector. The recombinant viruses were exposed to HE16 human embryonic fibroblasts. The expression levels of cone related genes were detected with real‐time PCR. We detected the activation of two of the photoreceptor‐related genes after the poly‐cistronic expression of CRX, RAX, NEURO‐D, and OTX2, but the rest of the genes did not exhibit transcriptional elevation. We concluded that the poly‐cistronic expression of CNROE induced partial reprogramming into photoreceptor cells. We hypothesize that the direct reprogramming into photoreceptor cells might require relatively high protein expression levels of transcriptional factors.
机译:摘要引入四个关键转录因子(CRX,rax,神经D,OTX2)允许成纤维细胞直接分化对视网膜感光体细胞。通过单位分子病毒的组合实现了这种重新编程。尽管单位分子病毒的组合是有用的,但是需要相对高的重组病毒,因为需要共感染。为了克服这一问题,我们建立了一种用于直接重编程的多位ronic表达系统,并在外源引入后分析了引入细胞的生物学特性。将4个重编程因子和EGFP(CRX,rax,Neuro-D,OTX2和EGFP; CNROE)的编码区域插入PMYS-IP逆转录病毒或CSII-CMV慢病毒载体的多个位点。将重组病毒暴露于He16人胚胎成纤维细胞。用实时PCR检测锥形相关基因的表达水平。我们在CRX,rax,神经-D和OTX2的多闭声表达后检测到两种感光相关基因的激活,但该基因的其余部分没有表现出转录升高。我们得出结论,CNROE诱导分级重新编程的多位式表达到感光细胞中。我们假设直接重新编程到光感受器细胞可能需要相对高的蛋白质表达水平的转录因子。

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