[基于iPS细胞的肌肉疾病治疗]。

Q4 Medicine
Hidetoshi Sakurai
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引用次数: 0

摘要

诱导多能干细胞(Induced pluripotent stem cells, iPSCs)由于其无限增殖和多能潜能,已被用于各种疑难疾病的治疗研究。我们的目标是通过细胞治疗和药物筛选两种途径,利用iPS细胞开发治疗顽固性肌肉疾病的新疗法。在这篇报告中,我将重点介绍细胞治疗的研究。我们已经开发了一种模拟发育阶段的分化诱导方法,并成功地诱导了适用于细胞移植治疗的骨骼肌干细胞。我们发现细胞移植到Duchenne肌营养不良(DMD)模型小鼠体内可再生10%以上的肌营养不良蛋白阳性纤维。此外,部分细胞已在体内作为卫星细胞移植,预计治疗效果将持续较长时间。至于对运动功能的影响,我们最近发现DMD模型小鼠体内dystrophin阳性肌纤维的再生主要是改善肌肉的疲劳耐受性,而不是最大收缩力。我们还开发了一种从ipsc诱导间充质间质细胞(MSCs)的分化方法。将ipsc来源的间充质干细胞(iMSCs)移植到Ullrich先天性肌营养不良(UCMD)模型小鼠中,可以恢复VI型胶原,从而增强肌肉再生。有趣的是,体细胞间充质干细胞,如骨髓源性间充质干细胞或脂肪源性间充质干细胞,即使通过移植也能恢复VI型胶原,但不具有治疗作用。我们最近发现了一种候选细胞,它负责肌肉再生,并在间充质干细胞中特异性表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[iPS cell-based therapy for muscular disorders].

Induced pluripotent stem cells (iPSCs) have been used in research for the development of treatments for various intractable diseases due to their unlimited proliferative and multipotent potential. We are aiming to develop novel therapies for intractable muscular diseases using iPS cells by two approaches i.e. cell therapy and drug screening. In this presentation, I focus on the cell therapy research. We have developed a differentiation induction method that mimics the developmental stages and have succeeded in inducing skeletal muscle stem cells that are applicable to cell transplantation therapy. We have found that cell transplantation into Duchenne muscular dystrophy (DMD) model mice is effective in regenerating more than 10% of dystrophin-positive fibers. In addition, some of the cells have been engrafted as satellite cells in vivo, and it is expected that the therapeutic effect will continue for a long period of time. As for the efficacy to the motor function, we have recently revealed that the regeneration of dystrophin positive myofibers in DMD model mice mainly ameliorates muscle fatigue tolerance rather than maximal contraction force in vivo. We have also developed a differentiation method to induce mesenchymal stromal cells (MSCs) from iPSCs. Transplantation of iPSC-derived MSCs (iMSCs) into Ullrich congenital muscular dystrophy (UCMD) model mice enabled the restoration of collagen type VI which resulted in enhancement of muscle regeneration. Interestingly, somatic MSCs such as bone marrow-derived MSC or adipose-derived MSC do not have therapeutic effect even they can also restore collagen type VI by the transplantation. We have recently found one of the candidates which is responsible for the muscle regeneration and is specifically expressed in the iMSCs.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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