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无酶超声分离细胞增强球状细胞聚集

Spheroid Cell Aggregation Enhanced by Enzyme-Free Ultrasound-Detached Cells.

作者信息

van Delft Julien, Imashiro Chikahiro, Kurashina Yuta, Hirano Makoto, Homma Jun, Mochizuki Shinsuke, Shimozawa Hideharu, Takemura Kenjiro

机构信息

Department of Mechanical Engineering, Keio University, 3-14-1 Hiyoshi Kohoku-ku, Yokohama, 223-8522, Japan.

School of Engineering, University of Tokyo, Tokyo, 113-8654, Japan.

出版信息

Adv Biol (Weinh). 2025 Aug;9(8):e00092. doi: 10.1002/adbi.202500092. Epub 2025 Aug 4.

Abstract

Spheroids are being widely studied as potential building blocks for complex organ engineering, tools for drug screening and cancer study. However, formation time has become the bottleneck of applications due to the need for large-scale high-quality spheroids production. Formation time is often dominated by ECM construction and not cell aggregation. Therefore, this study focuses on the influence of ultrasound detachment replacing conventional enzyme detachment on spheroid formation processes. Thanks to cell surface protein preservation in ultrasound detachment, cell aggregation time is reduced while decreasing the formation variabilities. Moreover, it is confirmed that cells are intrinsically more capable of aggregating through enzyme-free detachment. On top of that, transplantations into rats showed equally successful engraftment properties for enzyme-free detached cells. Finally, the impact on the real co-cultured spheroid application was shown to be beneficial through more localized cell groups inside of the spheroids, possibly improving therapeutic effects and vascularization. Through this study, it is proved that ultrasound detachment can replace enzyme detachment without degrading the final spheroid properties but reducing the formation time, and variability and improving robustness and cell distribution. This opens up a new range of applications for better and faster spheroid formation in numerous bioengineering applications.

摘要

球体作为复杂器官工程的潜在构建模块、药物筛选工具和癌症研究工具正受到广泛研究。然而,由于需要大规模高质量生产球体,形成时间已成为应用的瓶颈。形成时间通常由细胞外基质构建而非细胞聚集主导。因此,本研究聚焦于超声分离替代传统酶分离对球体形成过程的影响。得益于超声分离中细胞表面蛋白的保留,细胞聚集时间缩短,同时形成变异性降低。此外,证实细胞通过无酶分离在本质上更具聚集能力。除此之外,将细胞移植到大鼠体内显示,无酶分离的细胞具有同样成功的植入特性。最后,通过球体内部更局部化的细胞群,证明了对实际共培养球体应用的影响是有益的,这可能改善治疗效果和血管生成。通过本研究,证明了超声分离可替代酶分离,而不会降低最终球体特性,反而能缩短形成时间、降低变异性并提高稳健性和细胞分布。这为众多生物工程应用中更好更快地形成球体开辟了新的应用范围。

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