Influence of the static magnetic field on cell response in a miniaturized optically accessible bioreactor for 3D cell culture

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作者
Luca Izzo
Marta Tunesi
Lucia Boeri
Matteo Laganà
Carmen Giordano
Manuela Teresa Raimondi
机构
[1] Politecnico di Milano,Department of Chemistry, Materials and Chemical Engineering “G. Natta”
[2] Gemma Prototipi Studio,undefined
来源
Biomedical Microdevices | 2019年 / 21卷
关键词
MOAB; Static magnetic field; Perfusion bioreactors; Numerical characterization; 3D cell culture; Cell metabolic activity; Gene expression;
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摘要
Hydraulic sealing is a crucial condition for the maintenance of sterility during long term operation of microfluidic bioreactors. We developed a miniaturized optically accessible bioreactor (MOAB) allowing perfused culture of 3D cellularised constructs. In the MOAB, the culture chambers are sealed by magnets that generate a weak static magnetic field (SMF). Here, we predicted computationally the exact level of SMF to which cells are subjected during culture in the MOAB and we assessed its influence on the viability, metabolic activity and gene expression of neuroblastoma-derived cells cultured up to seven days. The predicted SMF ranged from 0.32 to 0.57 T using an axial-symmetric model of a single chamber, whereas it ranged from 0.35 to 0.62 T using a 3D model of the complete device. Cell function was evaluated in SH-SY5Y neuroblastoma cells at 2 and 7 days of culture in the MOAB, compared to 2D monolayer, 3D non-perfused constructs, and 3D perfused constructs cultured in a modified MOAB with magnet-free sealing. We measured the cell metabolic activity normalized by the DNA content and the expression levels of heat-shock protein 70 (Hsp-70), Bcl-2 and Bax. We found that the level of SMF applied to cells in the MOAB did not influence their metabolic activity and exerted a stressful effect in 2D monolayer, not confirmed in 3D conditions, neither static not perfused. Instead, the magnets provided a significantly greater hydraulic sealing in long-term culture, thus the MOAB might be potentially exploitable for the development of reliable in vitro models of neurodegeneration.
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