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用于人胚胎干细胞长期自我更新和心肌细胞分化的合成肽-丙烯酸盐表面。

Synthetic peptide-acrylate surfaces for long-term self-renewal and cardiomyocyte differentiation of human embryonic stem cells.

机构信息

Corning Life Sciences, Corning Inc., Corning, New York, USA.

出版信息

Nat Biotechnol. 2010 Jun;28(6):606-10. doi: 10.1038/nbt.1629. Epub 2010 May 30.

Abstract

Human embryonic stem cells (hESCs) have two properties of interest for the development of cell therapies: self-renewal and the potential to differentiate into all major lineages of somatic cells in the human body. Widespread clinical application of hESC-derived cells will require culture methods that are low-cost, robust, scalable and use chemically defined raw materials. Here we describe synthetic peptide-acrylate surfaces (PAS) that support self-renewal of hESCs in chemically defined, xeno-free medium. H1 and H7 hESCs were successfully maintained on PAS for over ten passages. Cell morphology and phenotypic marker expression were similar for cells cultured on PAS or Matrigel. Cells on PAS retained normal karyotype and pluripotency and were able to differentiate to functional cardiomyocytes on PAS. Finally, PAS were scaled up to large culture-vessel formats. Synthetic, xeno-free, scalable surfaces that support the self-renewal and differentiation of hESCs will be useful for both research purposes and development of cell therapies.

摘要

人胚胎干细胞(hESCs)具有两个对细胞治疗发展感兴趣的特性:自我更新和分化为人体所有主要体细胞谱系的潜力。hESC 衍生细胞的广泛临床应用将需要低成本、稳健、可扩展且使用化学定义的原材料的培养方法。在这里,我们描述了支持 hESCs 在化学定义的无饲养细胞培养基中自我更新的合成肽-丙烯酸盐表面(PAS)。H1 和 H7 hESCs 可在 PAS 上成功维持超过十代。在 PAS 上培养的细胞的形态和表型标志物表达与在 Matrigel 上培养的细胞相似。PAS 上的细胞保持正常核型和多能性,并能够在 PAS 上分化为功能心肌细胞。最后,PAS 被放大到大型培养容器格式。支持 hESCs 自我更新和分化的合成、无饲养细胞、可扩展的表面将有益于研究目的和细胞治疗的发展。

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