Journal of Embryo Transfer 2012; 27(3): 171-174
Published online September 30, 2012
Copyright © The Korean Society of Animal Reproduction and Biotechnology.
강호인, 노상호
서울대학교 치의학대학원 세포재프로그램 및 발생공학 연구실
Various small molecules can be used to control major signaling pathways to enhance stemness and inhibit differentiation in murine embryonic stem cell (mESC) culture. Small molecules inhibiting the fibroblast growth factor (FGF)/ERK pathway can preserve pluripotent cells from stimulation of differentiation. In this study, we aimed to evaluate the effect of pluripotin (SC-1), an inhibitor of the FGF/ERK pathway, on the colony formation of outgrowing presumptive mESCs. After plating the zona pellucida-free blastocyst on the feeder layer, attached cell clumps was cultured with SC-1 until the endpoint of the experiment at passage 10. In this experiment, when the number of colonies was counted at passage 3, SC-1-treated group showed 3.4 fold more mESC colonies when compared with control group. However, after passage 4, there was no stimulating effect of SC-1 on the colony formation. In conclusion, SC-1 treatment can be used to promote mESC generation by increasing the number of early mESC colonies.
Keywords: pluripotin (SC-1), small molecule, embryonic stem cells, mouse, FGF/ERK pathway
Journal of Embryo Transfer 2012; 27(3): 171-174
Published online September 30, 2012
Copyright © The Korean Society of Animal Reproduction and Biotechnology.
강호인, 노상호
서울대학교 치의학대학원 세포재프로그램 및 발생공학 연구실, 서울대학교 치의학대학원 세포재프로그램 및 발생공학 연구실
강호인, 노상호
서울대학교 치의학대학원 세포재프로그램 및 발생공학 연구실
Various small molecules can be used to control major signaling pathways to enhance stemness and inhibit differentiation in murine embryonic stem cell (mESC) culture. Small molecules inhibiting the fibroblast growth factor (FGF)/ERK pathway can preserve pluripotent cells from stimulation of differentiation. In this study, we aimed to evaluate the effect of pluripotin (SC-1), an inhibitor of the FGF/ERK pathway, on the colony formation of outgrowing presumptive mESCs. After plating the zona pellucida-free blastocyst on the feeder layer, attached cell clumps was cultured with SC-1 until the endpoint of the experiment at passage 10. In this experiment, when the number of colonies was counted at passage 3, SC-1-treated group showed 3.4 fold more mESC colonies when compared with control group. However, after passage 4, there was no stimulating effect of SC-1 on the colony formation. In conclusion, SC-1 treatment can be used to promote mESC generation by increasing the number of early mESC colonies.
Keywords: pluripotin (SC-1), small molecule, embryonic stem cells, mouse, FGF/ERK pathway
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pISSN: 2671-4639
eISSN: 2671-4663