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器官型培养物作为优化中枢神经系统细胞疗法的工具。

Organotypic cultures as tools for optimizing central nervous system cell therapies.

机构信息

INSERM U1066, 'Micro et Nanomédecines biomimétiques-MINT', Angers, France; LUNAM Université, Université Angers, UMR-S1066, Angers, France.

出版信息

Exp Neurol. 2013 Oct;248:429-40. doi: 10.1016/j.expneurol.2013.07.012. Epub 2013 Jul 27.

DOI:10.1016/j.expneurol.2013.07.012
PMID:23899655
Abstract

Stem cell therapy is a promising treatment for neurological disorders such as cerebral ischemia, Parkinson's disease and Huntington's disease. In recent years, many clinical trials with various cell types have been performed often showing mixed results. Major problems with cell therapies are the limited cell availability and engraftment and the reduced integration of grafted cells into the host tissue. Stem cell-based therapies can provide a limitless source of cells but survival and differentiation remain a drawback. An improved understanding of the behaviour of stem cells and their interaction with the host tissue, upon implantation, is needed to maximize the therapeutic potential of stem cells in neurological disorders. Organotypic cultures made from brain slices from specific brain regions that can be kept in culture for several weeks after injecting molecules or cells represent a remarkable tool to address these issues. This model allows the researcher to monitor/assess the behaviour and responses of both the endogenous as well as the implanted cells and their interaction with the microenvironment leading to cell engraftment. Moreover, organotypic cultures could be useful to partially model the pathological state of a disease in the brain and to study graft-host interactions prior to testing such grafts for pre-clinical applications. Finally, they can be used to test the therapeutic potential of stem cells when combined with scaffolds, or other therapeutic enhancers, among other aspects, needed to develop novel successful therapeutic strategies or improve on existing ones.

摘要

干细胞疗法是一种有前途的治疗方法,可用于治疗神经紊乱,如脑缺血、帕金森病和亨廷顿病。近年来,已经进行了许多使用各种细胞类型的临床试验,其结果通常喜忧参半。细胞疗法的主要问题是细胞可用性和植入的限制以及移植细胞与宿主组织的整合减少。基于干细胞的疗法可以提供无限的细胞来源,但细胞的存活和分化仍然是一个缺点。需要更好地了解干细胞的行为及其与宿主组织的相互作用,以最大限度地发挥干细胞在神经紊乱中的治疗潜力。从特定脑区的脑切片制成的器官型培养物可以在注入分子或细胞后在培养物中保存数周,这是解决这些问题的一个显著工具。该模型允许研究人员监测/评估内源性和植入细胞的行为和反应,以及它们与微环境的相互作用,从而导致细胞植入。此外,器官型培养物可用于部分模拟大脑中疾病的病理状态,并在进行临床前应用之前研究移植物-宿主相互作用。最后,当与支架或其他治疗增强剂结合使用时,它们可用于测试干细胞的治疗潜力,这是开发新的成功治疗策略或改进现有策略所必需的。

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