Furue Miho, Okamoto Tetsuji, Hayashi Yohei, Okochi Hitoshi, Fujimoto Manabu, Myoishi Yasufumi, Abe Takanori, Ohnuma Kiyoshi, Sato Gordon H, Asashima Makoto, Sato J Denry
Department of Biochemistry and Molecular Biology, Kanagawa Dental College, Yokosuka 238-8580, Japan.
In Vitro Cell Dev Biol Anim. 2005 Jan-Feb;41(1-2):19-28. doi: 10.1290/0502010.1.
We have developed a serum-free medium, designated ESF7, in which leukemia inhibitory factor (LIF) clearly stimulated murine embryonic stem (ES) cell proliferation accompanied by increased expression of nanog and Rex-1 and decreased FGF-5 expression. These effects were dependent on the concentration of LIF. The ES cells maintained in ESF7 medium for more than 2 yr retained an undifferentiated phenotype, as manifested by the expression of the transcription factor Oct-3/4, the stem cell marker SSEA-1, and alkaline phosphatase. Withdrawal of LIF from ESF7 medium resulted in ES cell apoptosis. Addition of serum to ESF7 medium promoted ES cell differentiation. Addition of BMP4 promoted ES cell differentiation into simple epithelial-like cells. In contrast, FGF-2 promoted ES cell differentiation into neuronal and glial-like cells. Under serum-free culture conditions, LIF was sufficient to stimulate cell proliferation, it inhibited cell differentiation, and it maintained self-renewal of ES cells. Because this simple serum-free adherent monoculture system supports the long-term propagation of pluripotent ES cells in vitro, it will allow the elucidation of ES cell responses to growth factors under defined conditions.
我们研发了一种无血清培养基,命名为ESF7,在该培养基中白血病抑制因子(LIF)能显著刺激小鼠胚胎干细胞(ES细胞)增殖,同时Nanog和Rex-1表达增加,FGF-5表达降低。这些效应依赖于LIF的浓度。在ESF7培养基中培养超过2年的ES细胞保持未分化表型,表现为转录因子Oct-3/4、干细胞标志物SSEA-1和碱性磷酸酶的表达。从ESF7培养基中撤除LIF会导致ES细胞凋亡。向ESF7培养基中添加血清会促进ES细胞分化。添加BMP4会促进ES细胞分化为简单的上皮样细胞。相反,FGF-2会促进ES细胞分化为神经元样和神经胶质样细胞。在无血清培养条件下,LIF足以刺激细胞增殖,抑制细胞分化,并维持ES细胞的自我更新。由于这种简单的无血清贴壁单培养系统支持多能ES细胞在体外长期增殖,它将有助于在特定条件下阐明ES细胞对生长因子的反应。