Induction of insulin-producing cells
    5.
    发明申请
    Induction of insulin-producing cells 审中-公开
    诱导产生胰岛素的细胞

    公开(公告)号:US20030219894A1

    公开(公告)日:2003-11-27

    申请号:US10413358

    申请日:2003-04-15

    IPC分类号: C12N005/08 C12N005/06

    摘要: What is described is a method for preparation of insulin-producing cells from non-insulin-producing cells. Mammalian fetal hepatocytes or hepatic progenitor cells are used ad the non-insulin-producing cells, and the method comprises culturing the mammalian fetal hepatocytes or the hepatic progenitor cells with 1-50 mmol/L of nicotinamide and concurrently bringing about expression of the PDX-1 gene or the NeuroD gene in the mammalian fetal hepatocytes.

    摘要翻译: 描述的是从非胰岛素生产细胞制备胰岛素生成细胞的方法。 使用哺乳动物胎儿肝细胞或肝祖细胞和非胰岛素产生细胞,并且该方法包括用1-50mmol / L的烟酰胺培养哺乳动物胎儿肝细胞或肝祖细胞,同时使PDX- 1基因或哺乳动物胎儿肝细胞中的NeuroD基因。

    Reprogramming cells for enhanced differentiation capacity using pluripotent stem cells
    6.
    发明申请
    Reprogramming cells for enhanced differentiation capacity using pluripotent stem cells 审中-公开
    使用多能干细胞重编程细胞增强分化能力

    公开(公告)号:US20030211603A1

    公开(公告)日:2003-11-13

    申请号:US10344680

    申请日:2003-02-12

    IPC分类号: C12N005/08

    摘要: Described in this disclosure is a new process whereby cells of one tissue type can be reprogrammed to produce cells of a different tissue type. Cells from a human donor are reprogrammed by culturing adjacent to primate pluripotent stem cells (in an undifferentiated or newly differentiated state) or in an environment supplemented by components taken from pPS cells. Simultaneously or in a subsequent step, the donor cells can be treated in a manner that enhances differentiation towards a different tissue type. In this manner, patients in need of tissue regeneration can be treated with cells differentiated and reprogrammed from their own autologous cell donation.

    摘要翻译: 在本公开中描述的是一种新方法,其中一种组织类型的细胞可以被重新编程以产生不同组织类型的细胞。 通过与灵长类多能干细胞(未分化或新分化状态)相邻的环境或在从由pPS细胞获取的组分补充的环境中培养来重新编程来自人供体的细胞。 同时或在随后的步骤中,供体细胞可以以增强朝不同组织类型分化的方式进行治疗。 以这种方式,需要组织再生的患者可以用从其自身的自体细胞捐献分化和重新编程的细胞来治疗。