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基质重塑增强了神经祖细胞在三维水凝胶中的分化能力。

Matrix Remodeling Enhances the Differentiation Capacity of Neural Progenitor Cells in 3D Hydrogels.

作者信息

Madl Christopher M, LeSavage Bauer L, Dewi Ruby E, Lampe Kyle J, Heilshorn Sarah C

机构信息

Department of Bioengineering Stanford University Stanford CA 94305 USA.

Department of Materials Science and Engineering Stanford University Stanford CA 94305 USA.

出版信息

Adv Sci (Weinh). 2019 Jan 11;6(4):1801716. doi: 10.1002/advs.201801716. eCollection 2019 Feb 20.

Abstract

Neural progenitor cells (NPCs) are a promising cell source to repair damaged nervous tissue. However, expansion of therapeutically relevant numbers of NPCs and their efficient differentiation into desired mature cell types remains a challenge. Material-based strategies, including culture within 3D hydrogels, have the potential to overcome these current limitations. An ideal material would enable both NPC expansion and subsequent differentiation within a single platform. It has recently been demonstrated that cell-mediated remodeling of 3D hydrogels is necessary to maintain the stem cell phenotype of NPCs during expansion, but the role of matrix remodeling on NPC differentiation and maturation remains unknown. By culturing NPCs within engineered protein hydrogels susceptible to degradation by NPC-secreted proteases, it is identified that a critical amount of remodeling is necessary to enable NPC differentiation, even in highly degradable gels. Chemical induction of differentiation after sufficient remodeling time results in differentiation into astrocytes and neurotransmitter-responsive neurons. Matrix remodeling modulates expression of the transcriptional co-activator Yes-associated protein, which drives expression of NPC stemness factors and maintains NPC differentiation capacity, in a cadherin-dependent manner. Thus, cell-remodelable hydrogels are an attractive platform to enable expansion of NPCs followed by differentiation of the cells into mature phenotypes for therapeutic use.

摘要

神经祖细胞(NPCs)是修复受损神经组织的一种很有前景的细胞来源。然而,扩增具有治疗相关性数量的NPCs并使其高效分化为所需的成熟细胞类型仍然是一项挑战。基于材料的策略,包括在3D水凝胶中培养,有可能克服当前的这些限制。一种理想的材料应能在单一平台上实现NPCs的扩增以及随后的分化。最近已经证明,细胞介导的3D水凝胶重塑对于在扩增过程中维持NPCs的干细胞表型是必要的,但基质重塑对NPCs分化和成熟的作用仍然未知。通过在易被NPCs分泌的蛋白酶降解的工程蛋白水凝胶中培养NPCs,发现即使在高度可降解的凝胶中,也需要一定量的关键重塑才能使NPCs分化。在足够的重塑时间后进行化学诱导分化会导致分化为星形胶质细胞和对神经递质有反应的神经元。基质重塑以钙黏蛋白依赖性方式调节转录共激活因子Yes相关蛋白的表达,该蛋白驱动NPCs干性因子的表达并维持NPCs的分化能力。因此,可被细胞重塑的水凝胶是一个有吸引力的平台,能够实现NPCs的扩增,随后将细胞分化为成熟表型以供治疗使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11cc/6382308/197972862729/ADVS-6-1801716-g001.jpg

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