期刊
ACTA BIOMATERIALIA
卷 16, 期 -, 页码 126-135出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2015.01.032
关键词
3D tissue model; Oxygen; Phosphorescence quenching microscopy; Porous membrane scaffold; PLIM
资金
- Science Foundation Ireland (SFI) [12/RC/2276, 13/SIRG/2144]
Porous membrane scaffolds are widely used materials for three-dimensional cell cultures and tissue models. Additional functional modification of such scaffolds can significantly extend their use and operational performance. Here we describe hybrid microporous polystyrene-based scaffolds impregnated with a phosphorescent O-2-sensitive dye PtTFPP, optimized for live cell fluorescence microscopy and imaging of O-2 distribution in cultured cells. Modified scaffolds possess high brightness, convenient spectral characteristics (534 nm excitation, 650 nm emission), stable and robust response to pO(2) in phosphorescence intensity and lifetime imaging modes (>twofold response over 21/0% O-2), such as confocal PUM. They are suitable for prolonged use under standard culturing conditions without affecting cell viability, and for multi-parametric imaging analysis of cultured cells and tissue samples. We tested the O-2 scaffolds with cultured cancer cells (HCF116), multicellular aggregates (PC12) and rat brain slices and showed that they can inform on tissue oxygenation at different depths and cell densities, changes in respiration activity, viability and responses to drug treatment. Using this method multiplexed with staining of dead cells (CellTox Green) and active mitochondria (TMRM), we demonstrated that decreased O-2 (20-24 mu M) in scaffold corresponds to highest expression of tyrosine hydroxylase in PC12 cells. Such hypoxia is also beneficial for action of hypoxia-specific anti-cancer drug tirapazamine (TPZ). Thus, O-2 scaffolds allow for better control of conditions in 3D tissue cultures, and are useful for a broad range of biomaterials and physiological studies. (C) 2015 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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