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通过多能干细胞定向诱导中脑和脊髓神经发生,在培养皿中模拟发育和疾病。

Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish.

作者信息

Allodi Ilary, Hedlund Eva

机构信息

Department of Neuroscience, Karolinska Institutet Stockholm, Sweden.

出版信息

Front Neurosci. 2014 May 20;8:109. doi: 10.3389/fnins.2014.00109. eCollection 2014.

Abstract

Induction of specific neuronal fates is restricted in time and space in the developing CNS through integration of extrinsic morphogen signals and intrinsic determinants. Morphogens impose regional characteristics on neural progenitors and establish distinct progenitor domains. Such domains are defined by unique expression patterns of fate determining transcription factors. These processes of neuronal fate specification can be recapitulated in vitro using pluripotent stem cells. In this review, we focus on the generation of dopamine neurons and motor neurons, which are induced at ventral positions of the neural tube through Sonic hedgehog (Shh) signaling, and defined at anteroposterior positions by fibroblast growth factor (Fgf) 8, Wnt1, and retinoic acid (RA). In vitro utilization of these morphogenic signals typically results in the generation of multiple neuronal cell types, which are defined at the intersection of these signals. If the purpose of in vitro neurogenesis is to generate one cell type only, further lineage restriction can be accomplished by forced expression of specific transcription factors in a permissive environment. Alternatively, cell-sorting strategies allow for selection of neuronal progenitors or mature neurons. However, modeling development, disease and prospective therapies in a dish could benefit from structured heterogeneity, where desired neurons are appropriately synaptically connected and thus better reflect the three-dimensional structure of that region. By modulating the extrinsic environment to direct sequential generation of neural progenitors within a domain, followed by self-organization and synaptic establishment, a reductionist model of that brain region could be created. Here we review recent advances in neuronal fate induction in vitro, with a focus on the interplay between cell intrinsic and extrinsic factors, and discuss the implications for studying development and disease in a dish.

摘要

在发育中的中枢神经系统中,特定神经元命运的诱导通过整合外在形态发生素信号和内在决定因素,在时间和空间上受到限制。形态发生素赋予神经祖细胞区域特征,并建立不同的祖细胞结构域。这些结构域由命运决定转录因子的独特表达模式所定义。使用多能干细胞可以在体外重现这些神经元命运特化的过程。在这篇综述中,我们重点关注多巴胺能神经元和运动神经元的生成,它们是通过音猬因子(Shh)信号在神经管腹侧位置诱导产生的,并由成纤维细胞生长因子(Fgf)8、Wnt1和视黄酸(RA)在前后位置进行定义。在体外利用这些形态发生信号通常会导致多种神经元细胞类型的产生,这些细胞类型在这些信号的交叉点处被定义。如果体外神经发生的目的只是生成一种细胞类型,那么可以通过在允许的环境中强制表达特定转录因子来进一步实现谱系限制。或者,细胞分选策略可以用于选择神经元祖细胞或成熟神经元。然而,在培养皿中模拟发育、疾病和前瞻性治疗可能会受益于结构化的异质性,即所需的神经元能够适当地形成突触连接,从而更好地反映该区域的三维结构。通过调节外在环境来指导在一个结构域内顺序生成神经祖细胞,随后进行自组织和突触建立,可以创建该脑区的简化模型。在这里我们综述了体外神经元命运诱导的最新进展,重点关注细胞内在和外在因素之间的相互作用,并讨论其对在培养皿中研究发育和疾病的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bde9/4033221/04cdd119cdcf/fnins-08-00109-g0001.jpg

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