METHOD AND COMPOSITION FOR INDUCING CHONDROGENESIS OR TENOGENESIS IN MESENCHYMAL STEM CELLS
    2.
    发明申请
    METHOD AND COMPOSITION FOR INDUCING CHONDROGENESIS OR TENOGENESIS IN MESENCHYMAL STEM CELLS 审中-公开
    在造血干细胞中诱导成纤维细胞或成骨细胞的方法和组合物

    公开(公告)号:WO2015082014A1

    公开(公告)日:2015-06-11

    申请号:PCT/EP2013/075782

    申请日:2013-12-06

    IPC分类号: C12N5/077 C12N5/0775

    摘要: The current invention concerns a cell medium for in vitro inducing chondrogenesis or tenogenesis in mesenchymal stem cells (MSCs), whereby said medium comprises a glucose medium supplemented with at least one growth factor, said growth factor is chosen from the group of fibroblast growth factors (FGF) or the group of transforming growth factors (TGF), characterized in that said FGF or TGF is present in a total concentration of between 1 and 15 ng/ml. In both cases, IGF can be added to enhance the induction process. In a further aspect, the invention provides for a use of such cell medium as well as a method for inducing isolated mesenchymal stem cells (MSCs) and a cell composition obtained by such method.

    摘要翻译: 本发明涉及用于体外诱导间充质干细胞(MSC)中的软骨形成或蜕变的细胞培养基,其中所述培养基包含补充至少一种生长因子的葡萄糖培养基,所述生长因子选自成纤维细胞生长因子 FGF)或转化生长因子(TGF)组,其特征在于所述FGF或TGFβ以1至15ng / ml的总浓度存在。 在这两种情况下,可以加入IGF以增强诱导过程。 在另一方面,本发明提供了这种细胞培养基的使用以及诱导分离的间充质干细胞(MSC)的方法和通过这种方法获得的细胞组合物。

    인간 배아 줄기 세포 또는 역분화 만능 줄기세포의 배양방법
    4.
    发明申请
    인간 배아 줄기 세포 또는 역분화 만능 줄기세포의 배양방법 审中-公开
    用于培养人胚胎干细胞或分化的PLUIPOTETI干细胞的方法

    公开(公告)号:WO2011055886A1

    公开(公告)日:2011-05-12

    申请号:PCT/KR2010/000969

    申请日:2010-02-17

    发明人: 이수홍 황승태

    IPC分类号: C12N5/074 C12N5/02

    摘要: 본 발명은 줄기세포 배양용 배지 중에서 인간 배아줄기세포 또는 역분화 만능 줄기세포를 배양하는 방법에 있어서, 상기 배지가 지지세포로서 세포성장억제제가 비-처리된 인간 지방 줄기 세포를 바닥면에 부착시킨 다공성 막을 포함하는 것을 특징으로 하는 배양방법 및 이를 이용한 인간 배아 줄기 세포 또는 역분화 만능 줄기세포의 회수방법을 제공한다.

    摘要翻译: 本发明涉及从用于干细胞培养的培养基中培养人胚胎干细胞或去分化多能干细胞的方法,其中由支持细胞组成的培养基包括多孔膜,细胞生长 抑制剂附着未经处理的人类脂肪干细胞。 本发明还涉及使用培养方法回收人胚胎干细胞或去分化多能干细胞的方法。

    METHODS OF MEDIATING MACROPHAGE PHENOTYPES
    8.
    发明申请
    METHODS OF MEDIATING MACROPHAGE PHENOTYPES 审中-公开
    介质加工方法

    公开(公告)号:WO2015081253A1

    公开(公告)日:2015-06-04

    申请号:PCT/US2014/067702

    申请日:2014-11-26

    IPC分类号: C12N5/0786

    摘要: Methods of inducing a polarization of macrophages. The method includes obtaining a blood fraction, fractionating the blood fraction to produce a blood fraction, and contacting the blood fraction with a source of macrophages. A blood fraction including platelet-poor plasma polarizes the source of macrophages into M1 macrophages. A blood faction including a protein solution polarizes the source of macrophages into M2 macrophages.

    摘要翻译: 诱导巨噬细胞极化的方法。 该方法包括获得血液分数,分馏血液部分以产生血液部分,并使血液部分与巨噬细胞源接触。 含血小板血浆的血液分数将巨噬细胞源极化为M1巨噬细胞。 包括蛋白质溶液在内的血液系将巨噬细胞的来源极化为M2巨噬细胞。

    CELL POPULATIONS HAVING IMMUNOREGULATORY ACTIVITY, METHODS FOR THE PREPARATION AND USES THEREOF
    10.
    发明申请
    CELL POPULATIONS HAVING IMMUNOREGULATORY ACTIVITY, METHODS FOR THE PREPARATION AND USES THEREOF 审中-公开
    具有免疫活性的细胞群体,其制备方法及其用途

    公开(公告)号:WO2012156522A1

    公开(公告)日:2012-11-22

    申请号:PCT/EP2012/059313

    申请日:2012-05-18

    发明人: DE LA ROSA, Olga

    摘要: The present invention provides isolated immunomodulatory cells, populations, compositions and therapeutic uses thereof. The immunomodulatory cells of the invention have surprising efficacy in the immunomodulation of multiple sclerosis. In one embodiment said immunomodulatory cells are regulatory T-cells, in a particularly preferred embodiment said immunomodulatory cells are Foxp3+CD4+CD25+ T- reg and/or IL-10/TGF-.beta.- producing regulatory Trl cells. Methods for the preparation, expansion and/or generation of immunomodulatory cells of the invention comprises contacting a cell population comprising of MSC and/or fibroblast cells with PBLs in the presence of one or more multiple sclerosis-associated antigens.

    摘要翻译: 本发明提供了分离的免疫调节细胞,种群,组合物和治疗用途。 本发明的免疫调节细胞在多发性硬化症的免疫调节中具有惊人的功效。 在一个实施方案中,所述免疫调节细胞是调节性T细胞,在特别优选的实施方案中,所述免疫调节细胞是Foxp3 + CD4 + CD25 + Treg和/或IL-10 / TGF-β。产生调节性Tr1细胞。 用于制备,扩增和/或产生本发明的免疫调节细胞的方法包括在一种或多种多发性硬化相关抗原存在下使包含MSC和/或成纤维细胞的细胞群与PBL接触。