Human embryonic germ cell line and methods of use
    92.
    发明授权
    Human embryonic germ cell line and methods of use 失效
    人胚胎生殖细胞系和使用方法

    公开(公告)号:US06245566B1

    公开(公告)日:2001-06-12

    申请号:US09052772

    申请日:1998-03-31

    IPC分类号: C12N502

    摘要: Primordial germ cells isolated from human embryonic tissue, such as from the gonadal ridges of human embryo, are disclosed. The primordial germ cells are cultured resulting in cells that resemble embryonic stem cells or embryonic germ cells in morphology and pluripotency. The cells are maintained several months in culture and can be genetically manipulated using transgenic technology to insert heterologous genetic material.

    摘要翻译: 公开了从人胚胎组织分离的原始生殖细胞,例如来自人胚胎的性腺脊髓。 培养原始生殖细胞,产生类似胚胎干细胞或胚胎生殖细胞的形态和多能性的细胞。 细胞在培养物中保持数月,可以使用转基因技术进行遗传操作以插入异源遗传物质。

    METHODS OF GENERATING INTERMEDIATE MESODERM CELLS FROM HUMAN PLURIPOTENT STEM CELLS
    98.
    发明申请
    METHODS OF GENERATING INTERMEDIATE MESODERM CELLS FROM HUMAN PLURIPOTENT STEM CELLS 审中-公开
    从人肺癌干细胞中产生中间粒细胞的方法

    公开(公告)号:US20160272937A1

    公开(公告)日:2016-09-22

    申请号:US15030315

    申请日:2014-04-14

    IPC分类号: C12N5/0735 A61K35/54

    摘要: Described herein are methods related to generating intermediate mesoderm (IM) cells, including using sequential treatment of small molecules and growth factors, and composition produced by the described methods. Using small molecules such as CHIR99021 in combination with FGF2 and RA, efficient differentiation of human pluripotent stem cells (hPSCs) into intermediate mesoderm, such as PAX2+LHX1+ cells, is achieved. The method is extensible different hPSC cell lines and does not require flow sorting. Importantly, resulting PAX2+LHX1+ cells, are capable of WT1 expression and addition of FGF9 and activin, PAX2+LHX1+ cells specifically differentiates cells into SIX2, SALL1, and WT1 expressing cells representative of cap mesenchyme nephron progenitor cells. The described methods and compositions facilitate and improve the directed differentiation of hPSCs into cells of the kidney lineage for the purposes of bioengineering kidney tissue and iPS cell disease modeling.

    摘要翻译: 本文描述了与产生中间胚层(IM)细胞相关的方法,包括使用小分子和生长因子的顺序处理以及由所述方法产生的组合物。 使用小分子如CHIR99021与FGF2和RA组合,实现人多能干细胞(hPSC)到中间胚层如PAX2 + LHX1 +细胞的有效分化。 该方法是可扩展的不同的hPSC细胞系,不需要流分选。 重要的是,所得到的PAX2 + LHX1 +细胞能够进行WT1表达,并加入FGF9和激活素,PAX2 + LHX1 +细胞将细胞特异性分化为表达帽间质肾单核祖细胞的SIX2,SALL1和WT1表达细胞。 所描述的方法和组合物促进和改善hPSC到肾脏谱系细胞的定向分化,用于生物工程肾组织和iPS细胞疾病建模。