4.7 Article

3D culture of fibroblasts and neuronal cells on microfabricated free-floating carriers

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 227, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.colsurfb.2023.113350

Keywords

3D cell culture; Bioprinting; Biofabrication; Cell carriers; CAD; PLGA; Silk fibroin

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3D cell culture is a technique that mimics in vivo environment for cells to grow in vitro. This study proposes two independent 3D cell culture models for different applications. One uses porous spherical structures as carriers to retain cell shape, while the other uses 3D printed silk fibroin structures for directed cell growth. These models have advantages in cell research, such as drug discovery and treatment of neuropathies.
3D cell culture is a relatively recent trend in biomedical research for artificially mimicking in vivo environment and providing three dimensions for the cells to grow in vitro, particularly with regard to surface-adherent mammalian cells. Different cells and research objectives require different culture conditions which has led to an increase in the diversity of 3D cell culture models. In this study, we show two independent on-carrier 3D cell culture models aimed at two different potential applications. Firstly, micron-scale porous spherical structures fabricated from poly (lactic-co-glycolic acid) or PLGA are used as 3D cell carriers so that the cells do not lose their physiologically relevant spherical shape. Secondly, millimetre-scale silk fibroin structures fabricated by 3D inkjet bioprinting are used as 3D cell carriers to demonstrate cell growth patterning in 3D for use in applications which require directed cell growth. The L929 fibroblasts demonstrated excellent adherence, cell-division and proliferation on the PLGA carriers, while the PC12 neuronal cells showed excellent adherence, proliferation and spread on the fibroin carriers without any evidence of cytotoxicity from the carriers. The present study thus proposes two models for 3D cell culture and demonstrates, firstly, that easily fabricable porous PLGA structures can act as excellent cell carriers for aiding cells easily retain their physiologically relevant 3D spherical shape in vitro, and secondly, that 3D inkjet printed silk fibroin structures can act as geometrically-shaped carriers for 3D cell patterning or directed cell growth in vitro. While the 'fibroblasts on PLGA carriers' model will help achieve more accurate results than the conventional 2D culture in cell research, such as drug discovery, and cell proliferation for adoptive cell transfer, such as stem cell therapy, the 'neuronal cells on silk fibroin carriers' model will help in research requiring patterned cell growth, such as treatment of neuropathies.

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