Nanog is a recently discovered homeodomain transcription factor that sustains the pluripotency of embryonic stem (ES) cells and blocks their differentiation into endoderm. The murine F9 embryonal carcinoma cell line...Nanog is a recently discovered homeodomain transcription factor that sustains the pluripotency of embryonic stem (ES) cells and blocks their differentiation into endoderm. The murine F9 embryonal carcinoma cell line is a well-documented model system for endoderm cell lineage differentiation. Here, we examined the function of Nanog in F9 cell endoderm differentiation. Over-expression of Nanog returns the F9 cells to the early status of ES cells and represses the differentiation of primitive endoderm and parietal endoderm in F9 cells, whereas it has no effect on the differentiation of visceral endoderm. In contrast, the expression of C-terminal domain-truncated Nanog spontaneously promotes endoderm differentiation in F9 cells. These data suggest that Nanog is required to sustain the proper undifferentiated status of F9 cells, and the C-terminal domain of Nanog transduces the most effects in repressing primitive endoderm and parietal endoderm differentiation in F9 cells.展开更多
目的观察低氧对P19细胞神经分化的影响,针对其向多巴胺能神经元分化的现象及机制进行探讨。方法实验分为常氧组(20%O2)和低氧组(3%O2,每天低氧10 m in)。对诱导分化的神经元采用免疫细胞化学染色方法鉴定。用流式细胞术及W estern b lo...目的观察低氧对P19细胞神经分化的影响,针对其向多巴胺能神经元分化的现象及机制进行探讨。方法实验分为常氧组(20%O2)和低氧组(3%O2,每天低氧10 m in)。对诱导分化的神经元采用免疫细胞化学染色方法鉴定。用流式细胞术及W estern b lot检测多巴胺能神经元,高效液相色谱法测定分泌的多巴胺。用RT-PCR技术检测低氧诱导因子HIF-1αmRNA水平。结果①在分化的P19细胞中,低氧组神经元含量高于常氧组(P<0.05),低氧组多巴胺能神经元含量及所分泌的多巴胺显著高于常氧组(P<0.001);②低氧组诱导期HIF-1αmRNA表达水平明显高于常氧组。结论低氧可以促进P19细胞的神经分化,尤其促进P19细胞向多巴胺能神经元分化,HIF-1α可能在其中起了一定作用。展开更多
Nanog protein is expressed in the interior cells of compacted morulae and maintained till epiblasts but downregulated by implantation stage. It is also expressed in embryonic stem cells, embryonic carcinoma cells and ...Nanog protein is expressed in the interior cells of compacted morulae and maintained till epiblasts but downregulated by implantation stage. It is also expressed in embryonic stem cells, embryonic carcinoma cells and embryonic germ cells but disappeared in differentiated ES cells. In this study, we have isolated, sequenced, and performed the first characterization of the Nanog promoter. The transcription start sites were mapped by primer extension analysis. Two promoter regions were found upstream the transcription start sites and the expression of major Nanog promoter/ reporter gene construct is abolished in differentiated F9 EC cells as compared to the undifferentiated counterpart. We also showed that a putative octamer motif (ATGCAAAA) is necessary for the major promoter activity. Gel shift and supershift assays showed that Oct-1, Oct-4 and Oct-6 protein selectively bind to the octamer motif.展开更多
文摘Nanog is a recently discovered homeodomain transcription factor that sustains the pluripotency of embryonic stem (ES) cells and blocks their differentiation into endoderm. The murine F9 embryonal carcinoma cell line is a well-documented model system for endoderm cell lineage differentiation. Here, we examined the function of Nanog in F9 cell endoderm differentiation. Over-expression of Nanog returns the F9 cells to the early status of ES cells and represses the differentiation of primitive endoderm and parietal endoderm in F9 cells, whereas it has no effect on the differentiation of visceral endoderm. In contrast, the expression of C-terminal domain-truncated Nanog spontaneously promotes endoderm differentiation in F9 cells. These data suggest that Nanog is required to sustain the proper undifferentiated status of F9 cells, and the C-terminal domain of Nanog transduces the most effects in repressing primitive endoderm and parietal endoderm differentiation in F9 cells.
文摘目的观察低氧对P19细胞神经分化的影响,针对其向多巴胺能神经元分化的现象及机制进行探讨。方法实验分为常氧组(20%O2)和低氧组(3%O2,每天低氧10 m in)。对诱导分化的神经元采用免疫细胞化学染色方法鉴定。用流式细胞术及W estern b lot检测多巴胺能神经元,高效液相色谱法测定分泌的多巴胺。用RT-PCR技术检测低氧诱导因子HIF-1αmRNA水平。结果①在分化的P19细胞中,低氧组神经元含量高于常氧组(P<0.05),低氧组多巴胺能神经元含量及所分泌的多巴胺显著高于常氧组(P<0.001);②低氧组诱导期HIF-1αmRNA表达水平明显高于常氧组。结论低氧可以促进P19细胞的神经分化,尤其促进P19细胞向多巴胺能神经元分化,HIF-1α可能在其中起了一定作用。
文摘Nanog protein is expressed in the interior cells of compacted morulae and maintained till epiblasts but downregulated by implantation stage. It is also expressed in embryonic stem cells, embryonic carcinoma cells and embryonic germ cells but disappeared in differentiated ES cells. In this study, we have isolated, sequenced, and performed the first characterization of the Nanog promoter. The transcription start sites were mapped by primer extension analysis. Two promoter regions were found upstream the transcription start sites and the expression of major Nanog promoter/ reporter gene construct is abolished in differentiated F9 EC cells as compared to the undifferentiated counterpart. We also showed that a putative octamer motif (ATGCAAAA) is necessary for the major promoter activity. Gel shift and supershift assays showed that Oct-1, Oct-4 and Oct-6 protein selectively bind to the octamer motif.