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用于构建微纤维筏以在动态悬浮中扩增多能干细胞的超分子添加剂筛选

Supramolecular Additive Screening to Engineer Microfibrous Rafts for Expansion of Pluripotent Stem Cells in Dynamic Suspension.

作者信息

van Sprang Johnick F, Aarts Jasper G M, Arts Boris, Brouns Joyce E P, Komil Muhabbat I, Bartels Paul A A, Dankers Patricia Y W

机构信息

Institute for Complex Molecular Systems, and Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, 5612AZ, The Netherlands.

出版信息

Adv Healthc Mater. 2025 Apr;14(11):e2404186. doi: 10.1002/adhm.202404186. Epub 2025 Mar 10.

Abstract

Human induced pluripotent stem cells (hiPSCs) hold the potential to generate any human tissue for transplantation in regenerative therapies. These complex cell therapies require billions of cells, which is challenging to acquire in planar adherent cultures. Transitioning hiPSCs to 3D suspension culture on microcarrier materials, often bead-shaped, improves the total surface area accessible to cells, thereby enabling culture scale-up. However, bead-shaped microcarriers do not have the optimal shape configuration, because it is the lowest surface-to-volume ratio of all geometrical shapes, and it also induces uncontrolled cell clumping. Application of synthetic, microfibrous rafts as a replacement for bead-shaped microcarriers potentially solves these issues. Here, microfibrous rafts are engineered by first screening a supramolecular biomaterial library composed of bisurea (BU)-peptide conjugate additives for its ability to induce hiPSC adhesion and maintenance of its pluripotent state, followed by electrospinning the screening-hit into raft-like structures. The resulting rafts contain cylinder-like microfibers, which have a higher surface-to-volume ratio compared to conventional bead-shaped microcarriers, and the flat configuration of the rafts prevents clumping.

摘要

人类诱导多能干细胞(hiPSC)有潜力生成任何用于再生疗法移植的人体组织。这些复杂的细胞疗法需要数十亿个细胞,而在平面贴壁培养中获取这些细胞具有挑战性。将hiPSC过渡到通常呈珠状的微载体材料上的3D悬浮培养,可以增加细胞可利用的总表面积,从而实现培养规模的扩大。然而,珠状微载体并不具有最佳的形状结构,因为它是所有几何形状中表面积与体积比最低的,而且还会导致细胞不受控制地聚集。应用合成的微纤维筏作为珠状微载体的替代品可能会解决这些问题。在此,通过首先筛选由双脲(BU)-肽共轭添加剂组成的超分子生物材料库诱导hiPSC粘附及其多能状态维持的能力,然后将筛选出的材料静电纺丝成筏状结构,来制造微纤维筏。所得的筏含有圆柱状微纤维,与传统的珠状微载体相比,其表面积与体积比较高,并且筏的扁平结构可防止聚集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af5b/12023819/eb59b2076aab/ADHM-14-0-g003.jpg

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