4.7 Review

Cell spheroids as a versatile research platform: formation mechanisms, high throughput production, characterization and applications

期刊

BIOFABRICATION
卷 13, 期 3, 页码 -

出版社

IOP Publishing Ltd
DOI: 10.1088/1758-5090/abe6f2

关键词

cell spheroids; cell aggregation; 3D cell culture; spheroids as in vitro models; tissue engineering; drug screening; 3D bioprinting

资金

  1. National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico-CNPq, Brazil) [307829/2018-9, 430860/2018-8, 142050/2018-0]
  2. Coordination for the Improvement of Higher Educational Personnel (CoordenacAo de Aperfeicoamento de Pessoal de Nivel Superior-CAPES, Brazil) [001, PrInt 88887.364849/2019-00, PrInt 88887.310405/2018-00]
  3. University of Campinas(Fundo de Apoio ao Ensino, a Pesquisa e a ExtensAo-FAEPEX/UNICAMP, Brazil) [2921/18]
  4. SAo Paulo Research Foundation (FundacAo de Amparo a Pesquisa do Estado de SAo Paulo-FAPESP, Brazil) [2019/11950-6, 2015/05102-1]
  5. Dutch Province of Limburg

向作者/读者索取更多资源

Three-dimensional (3D) cell culture, especially using spheroids, is a powerful tool for mimicking the in vivo structure and microenvironment of healthy tissues and solid tumors. Engineering processes to obtain uniform 3D cell spheroids, considering mass transfer and shear stress, as well as computational and mathematical modeling, are important for developing large tissues and complex organs. Challenges in analyzing morphological parameters, cell quantification, viability, gene expression profiles, metabolic behavior, and high-content analysis need to be addressed to maximize the potential applications of spheroids in various research fields.
Three-dimensional (3D) cell culture has tremendous advantages to closely mimic the in vivo architecture and microenvironment of healthy tissue and organs, as well as of solid tumors. Spheroids are currently the most attractive 3D model to produce uniform reproducible cell structures as well as a potential basis for engineering large tissues and complex organs. In this review we discuss, from an engineering perspective, processes to obtain uniform 3D cell spheroids, comparing dynamic and static cultures and considering aspects such as mass transfer and shear stress. In addition, computational and mathematical modeling of complex cell spheroid systems are discussed. The non-cell-adhesive hydrogel-based method and dynamic cell culture in bioreactors are focused in detail and the myriad of developed spheroid characterization techniques is presented. The main bottlenecks and weaknesses are discussed, especially regarding the analysis of morphological parameters, cell quantification and viability, gene expression profiles, metabolic behavior and high-content analysis. Finally, a vast set of applications of spheroids as tools for in vitro study model systems is examined, including drug screening, tissue formation, pathologies development, tissue engineering and biofabrication, 3D bioprinting and microfluidics, together with their use in high-throughput platforms.

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