[iPS细胞技术在生活方式疾病中的应用]。

Clinical calcium Pub Date : 2016-03-01
Yasuhiro Takashima
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摘要

目前,利用诱导多能干细胞来了解生活方式疾病的病理尚不成熟,因为生活方式疾病与诱导多能干细胞之间的直接联系部分较少。因此,越来越多的科学家关注再生医学,比如利用iPS细胞技术进行β细胞治疗。即使在2型糖尿病患者中,胰岛β细胞分泌的胰岛素减少也是原因之一,因此从iPS细胞中生成β细胞将是一个强有力的工具。另一个原因是生活方式疾病的病理复杂性。导致生活方式疾病的原因有很多。生活方式疾病包括癌症、慢性肝病、2型糖尿病、心脏病、代谢综合征、慢性肾衰竭、中风和肥胖。由于肥胖是生活方式疾病的主要原因之一,我们希望在本综述中重点关注iPS细胞的脂肪生成。我们分析并建立了小鼠胚胎干细胞和人iPS细胞向脂肪细胞的分化方案。本综述的另一个重点是多能细胞的起始分化。多能干细胞的质量是获得高分化细胞的关键因素之一。最近,我们开发了一种新的幼稚人多能干细胞(PSC),“重置细胞”。与传统的人PSC相比,幼稚的PSC与人的表母细胞更相似。由于它们的低甲基化状态和较早的发育阶段,它们将是更理想的分化细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Application for Lifestyle disease by iPS cells technologies].

Currently it is less advanced to understand the pathology of lifestyle disease by using iPS cells because there is partly less direct connection between life style disease and iPS cells. So much more scientists focus on regenerative medicine such as beta cells therapy using iPS cells technologies. It will be indeed a powerful tool to generate beta cells from iPS cells as even in type2 diabetes patients, hyposecretion of insulin from beta cells in pancreas is one of causes. Another reason is complexity of the pathology of life style disease. There are a lot of reasons to cause lifestyle disease. Lifestyle diseases include cancer, chronic liver disease, Type 2 diabetes, heart disease, metabolic syndrome, chronic renal failure, stroke, and obesity. Since obesity is one of major causes of lifestyle diseases, we want to focus on adipogenesis from iPS cells in this review. We analysed and established the differentiation protocol into adipocytes from mouse ES cells and human iPS cells. The other point in this review is the starting pluripotent cells for differentiation. Quality of pluripotent stem cells are one of most critical factors to succeed in getting well-differentiated cells. Recently, we have developed new naive human pluripotent stem cells (PSC),"Reset cells". Naive PSC have more similar to human epibast cells than conventional human PSC. They will be more ideal cells for differentiation because of their hypomethylated status and earlier stage of development.

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