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用于同质多细胞肿瘤球体群体生长和分析的微结构软设备。

Microstructured soft devices for the growth and analysis of populations of homogenous multicellular tumor spheroids.

机构信息

Department of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy.

Department of Electronics Technology, Budapest University of Technology and Economics, Budapest, Hungary.

出版信息

Cell Mol Life Sci. 2023 Mar 16;80(4):93. doi: 10.1007/s00018-023-04748-1.

Abstract

Multicellular tumor spheroids are rapidly emerging as an improved in vitro model with respect to more traditional 2D culturing. Microwell culturing is a simple and accessible method for generating a large number of uniformly sized spheroids, but commercially available systems often do not enable researchers to perform complete culturing and analysis pipelines and the mechanical properties of their culture environment are not commonly matching those of the target tissue. We herein report a simple method to obtain custom-designed self-built microwell arrays made of polydimethylsiloxane or agarose for uniform 3D cell structure generation. Such materials can provide an environment of tunable mechanical flexibility. We developed protocols to culture a variety of cancer and non-cancer cell lines in such devices and to perform molecular and imaging characterizations of the spheroid growth, viability, and response to pharmacological treatments. Hundreds of tumor spheroids grow (in scaffolded or scaffold-free conditions) at homogeneous rates and can be harvested at will. Microscopy imaging can be performed in situ during or at the end of the culture. Fluorescence (confocal) microscopy can be performed after in situ staining while retaining the geographic arrangement of spheroids in the plate wells. This platform can enable statistically robust investigations on cancer biology and screening of drug treatments.

摘要

多细胞肿瘤球体在越来越多地被视为一种优于传统二维培养的改进型体外模型。微孔培养是一种生成大量大小均匀球体的简单且易于使用的方法,但市售系统通常无法让研究人员完成完整的培养和分析流程,并且其培养环境的机械性能通常与目标组织不匹配。本文报道了一种简单的方法,可以获得由聚二甲基硅氧烷或琼脂糖制成的定制设计的自组装微井阵列,以均匀生成 3D 细胞结构。这些材料可以提供可调节机械灵活性的环境。我们开发了在这些设备中培养各种癌症和非癌细胞系的方案,并对球体生长、活力和对药物治疗的反应进行分子和成像特征分析。数百个肿瘤球体以均匀的速度生长(在有或没有支架的条件下),并且可以随时收获。可以在培养过程中或结束时进行原位显微镜成像。可以在原位染色后进行荧光(共聚焦)显微镜检查,同时保留板孔中球体的地理排列。该平台可以实现对癌症生物学的统计学稳健研究和药物治疗的筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d10c/11073294/12aaea9fb18b/18_2023_4748_Fig1_HTML.jpg

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