诱导多能干细胞的衍生及其治疗潜力

Lin Yang, M. Lau, H. Ng
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摘要

利用已定义的转录因子对体细胞进行重编程的成功为产生具有潜在治疗目的的患者特异性诱导多能干细胞(iPS)奠定了基础。尽管iPS细胞技术对再生医学有很大的前景,但目前的iPS细胞衍生方法仍处于起步阶段,尚未对安全可靠地生产临床级多能细胞进行优化。自2006年iPS细胞技术问世以来,在解决iPS细胞生成方法的缺陷方面取得了快速进展。在本文中,我们回顾了影响该领域方向的关键研究,比较了诱导多能干细胞形成的各种方法,并展望了诱导多能干细胞为研究和临床目的提供的可能性。
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DERIVATION AND THERAPEUTIC POTENTIALS OF INDUCED PLURIPOTENT STEM CELLS
The success of somatic cell reprogramming using defined transcription factors has laid the groundwork for generation of patient-specific induced pluripotent stem (iPS) cells for potential therapeutic purposes. Despite the promises iPS cell technology holds for regenerative medicine, current iPS cell derivation methods are still in infancy stages and have yet to be optimized for the safe and reliable production of clinical-grade pluripotent cells. Since the inception of iPS cell technology in 2006, rapid progress has been made to address the drawbacks implicated in iPS cell genesis methods. In this article, we review the key studies which have shaped the direction of the field, compare the various methods of iPS cell genesis and look ahead to the possibilities iPS cells offer for both research and clinical purposes.
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NUCLEAR REPROGRAMMING AND THE CURRENT CHALLENGES IN ADVANCING PERSONALIZED PLURIPOTENT STEM CELL-BASED THERAPIES S/MAR VECTORS — ALTERNATIVE EXPRESSION SYSTEMS FOR GENE THERAPY? MURINE PGK PROMOTER IN A LENTIVIRAL VECTOR IN CANINE LEUKOCYTE ADHESION DEFICIENCY AND IN HUMAN LAD-1 CD34+ CELLS IN NSG MICE 3D CELL BIOPRINTING FOR REGENERATIVE MEDICINE RESEARCH AND THERAPIES EDITORIAL — NOBEL PRIZE HIGHLIGHT: SOMATIC CELL REPROGRAMMING AND THE CURRENT CLINICAL GRADE CHALLENGE
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