Southwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Methods Mol Biol. 2022;2389:165-175. doi: 10.1007/978-1-0716-1783-0_14.
Neural stem cell therapy has been galvanized by the discovery of pluripotent stem cells. The possibility to generate specialized central nervous system-specific differentiated cells using human somatic cells engineered to become induced pluripotent stem cells (iPSCs) was a game changer. This technology has broad applications in the field of regenerative medicine, in vitro disease modeling, targeted drug discovery, and precision medicine. Currently, iPSCs are one of the most promising cell sources amenable for commercialization and off-the-shelf neural stem cell therapy products. iPSCs exhibit a strong self-renewable ability that supports the development of a virtually unlimited source of neural cells for structural repair in neurological disorders. However, along with this strong proliferative capacity of iPSCs comes the tumorigenic potential of these cells after transplantation. Thus, the isolation and purification of a homogeneous population of human neural stem cells (hNSCs) are of paramount importance to ensure consistency in the composition of the cellular product and to avoid tumor formation in the host brain. This chapter describes the isolation, neuralization, and long-term perpetuation of hNSCs derived from iPSCs through the use of specific growth medium and the preparation of hNSCs for transplantation in an experimental model of stroke. Additionally, we will describe methods to analyze the ischemic stroke and size of grafts using magnetic resonance imaging and OsiriX software and neuroanatomical tracing procedures to study axonal remodeling after ischemic stroke and cell transplantation.
神经干细胞疗法因多能干细胞的发现而备受关注。利用人类体细胞工程化成为诱导多能干细胞(iPSC),产生专门的中枢神经系统特异性分化细胞的可能性是一个重大突破。这项技术在再生医学、体外疾病建模、靶向药物发现和精准医学等领域具有广泛的应用。目前,iPSC 是最有前途的细胞来源之一,适用于商业化和现成的神经干细胞治疗产品。iPSC 表现出强大的自我更新能力,支持为神经退行性疾病的结构修复开发几乎无限的神经细胞来源。然而,随着 iPSC 强大的增殖能力,这些细胞在移植后存在致瘤潜能。因此,分离和纯化同质的人神经干细胞(hNSC)群对于确保细胞产品成分的一致性以及避免宿主大脑中的肿瘤形成至关重要。本章描述了通过使用特定的生长培养基从 iPSC 中分离、神经化和长期维持 hNSC 的方法,并介绍了用于移植到缺血性中风实验模型中的 hNSC 的制备方法。此外,我们还将描述使用磁共振成像和 OsiriX 软件分析缺血性中风和移植物大小的方法,以及神经解剖追踪程序来研究缺血性中风和细胞移植后的轴突重塑。