Shi Tianyuan, Cheung Martin
School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Cell Biosci. 2021 May 13;11(1):85. doi: 10.1186/s13578-021-00594-5.
Neurological diseases are mainly modeled using rodents through gene editing, surgery or injury approaches. However, differences between humans and rodents in terms of genetics, neural development, and physiology pose limitations on studying disease pathogenesis in rodent models for neuroscience research. In the past decade, the generation of induced pluripotent stem cells (iPSCs) and induced neural stem cells (iNSCs) by reprogramming somatic cells offers a powerful alternative for modeling neurological diseases and for testing regenerative medicines. Among the different somatic cell types, urine-derived stem cells (USCs) are an ideal cell source for iPSC and iNSC reprogramming, as USCs are highly proliferative, multipotent, epithelial in nature, and easier to reprogram than skin fibroblasts. In addition, the use of USCs represents a simple, low-cost and non-invasive procedure for generating iPSCs/iNSCs. This review describes the cellular and molecular properties of USCs, their differentiation potency, different reprogramming methods for the generation of iPSCs/iNSCs, and their potential applications in modeling neurological diseases.
神经疾病主要通过基因编辑、手术或损伤方法利用啮齿动物进行建模。然而,人类和啮齿动物在遗传学、神经发育和生理学方面的差异对神经科学研究中在啮齿动物模型中研究疾病发病机制构成了限制。在过去十年中,通过重编程体细胞产生诱导多能干细胞(iPSC)和诱导神经干细胞(iNSC)为神经疾病建模和测试再生药物提供了一种强大的替代方法。在不同的体细胞类型中,尿液衍生干细胞(USC)是iPSC和iNSC重编程的理想细胞来源,因为USC具有高度增殖性、多能性、本质上是上皮细胞,并且比重编程皮肤成纤维细胞更容易。此外,使用USC代表了一种简单、低成本且非侵入性的生成iPSC/iNSC的方法。本综述描述了USC的细胞和分子特性、它们的分化潜能、生成iPSC/iNSC的不同重编程方法,以及它们在神经疾病建模中的潜在应用。