| Literature DB >> 33592595 |
Monize Caiado Decarli1,2, Robson Amaral3, Diogo Peres Dos Santos4, Larissa Bueno Tofani3, Eric Katayama4, Rodrigo Alvarenga Rezende5, Jorge Vicente Lopes da Silva5, Kamilla Swiech3, Claudio Alberto Torres Suazo4, Carlos Mota2, Lorenzo Moroni2, Ângela Maria Moraes1.
Abstract
Three-dimensional (3D) cell culture has tremendous advantages to closely mimic thein vivoarchitecture 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 forin vitrostudy 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.Entities:
Keywords: 3D bioprinting; 3D cell culture; cell aggregation; cell spheroids; drug screening; spheroids as in vitro models; tissue engineering
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Year: 2021 PMID: 33592595 DOI: 10.1088/1758-5090/abe6f2
Source DB: PubMed Journal: Biofabrication ISSN: 1758-5082 Impact factor: 9.954