
Live microscopy of multicellular spheroids with the multimodal near-infrared nanoparticles reveals differences in oxygenation gradients
- Author
- Angela Debruyne (UGent) , Irina Okkelman (UGent) , Nina Heymans (UGent) , Cláudio Pinheiro (UGent) , An Hendrix (UGent) , Max Nobis, Sergey M. Borisov and Ruslan Dmitriev (UGent)
- Organization
- Project
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- Next generation biosensors for luminescence lifetime imaging-assisted organoid engineering
- White light laser-based confocal fluorescence lifetime imaging microscope for multi-parameter 3D live imaging
- Doctoral Network for a Shared Excellence of Fluorescent Lifetime Imaging Microscopy in Biomedical Applications
- Abstract
- Assessment of hypoxia, nutrients, metabolite gradients, and other hallmarks of the tumor microenvironment within 3D multicellular spheroid and organoid models represents a challenging analytical task. Here, we report red/near-infrared (NIR) emitting cell staining with O2-sensitive nanoparticles, which enable measurements of spheroid oxygenation on a conventional fluorescence microscope. Nanosensor probes, termed “MMIR” (multimodal infrared), incorporate an NIR O2-sensitive metalloporphyrin (PtTPTBPF) and deep red aza-BODIPY reference dyes within a biocompatible polymer shell, allowing for oxygen gradient quantification via fluorescence ratio and phosphorescence lifetime readouts. We optimized staining techniques and evaluated the nanosensor probe characteristics and cytotoxicity. Subsequently, we applied nanosensors to the live spheroid models based on HCT116, DPSCs, and SKOV3 cells, at rest, and treated with drugs affecting cell respiration. We found that the growth medium viscosity, spheroid size, and formation method influenced spheroid oxygenation. Some spheroids produced from HCT116 and dental pulp stem cells exhibited “inverted” oxygenation gradients, with higher core oxygen levels than the periphery. This contrasted with the frequently encountered “normal” gradient of hypoxia toward the core caused by diffusion. Further microscopy analysis of spheroids with an “inverted” gradient demonstrated metabolic stratification of cells within spheroids: thus, autofluorescence FLIM of NAD(P)H indicated the formation of a glycolytic core and localization of OxPhos-active cells at the periphery. Collectively, we demonstrate a strong potential of NIR-emitting ratiometric nanosensors for advanced microscopy studies targeting live and quantitative real-time monitoring of cell metabolism and hypoxia in complex 3D tissue models.
- Keywords
- oxygenation, nanoparticles, multicellularspheroids, FLIM, fluorescence microscopy, hypoxia, cancer
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2024 Debruyne-et-al-2024-live-microscopy-of-multicellular-spheroids ACS Nano.pdf
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01HWZB92HHDQZYPR3SNAY6RHZX
- MLA
- Debruyne, Angela, et al. “Live Microscopy of Multicellular Spheroids with the Multimodal Near-Infrared Nanoparticles Reveals Differences in Oxygenation Gradients.” ACS NANO, vol. 18, no. 19, 2024, pp. 12168–86, doi:10.1021/acsnano.3c12539.
- APA
- Debruyne, A., Okkelman, I., Heymans, N., Pinheiro, C., Hendrix, A., Nobis, M., … Dmitriev, R. (2024). Live microscopy of multicellular spheroids with the multimodal near-infrared nanoparticles reveals differences in oxygenation gradients. ACS NANO, 18(19), 12168–12186. https://doi.org/10.1021/acsnano.3c12539
- Chicago author-date
- Debruyne, Angela, Irina Okkelman, Nina Heymans, Cláudio Pinheiro, An Hendrix, Max Nobis, Sergey M. Borisov, and Ruslan Dmitriev. 2024. “Live Microscopy of Multicellular Spheroids with the Multimodal Near-Infrared Nanoparticles Reveals Differences in Oxygenation Gradients.” ACS NANO 18 (19): 12168–86. https://doi.org/10.1021/acsnano.3c12539.
- Chicago author-date (all authors)
- Debruyne, Angela, Irina Okkelman, Nina Heymans, Cláudio Pinheiro, An Hendrix, Max Nobis, Sergey M. Borisov, and Ruslan Dmitriev. 2024. “Live Microscopy of Multicellular Spheroids with the Multimodal Near-Infrared Nanoparticles Reveals Differences in Oxygenation Gradients.” ACS NANO 18 (19): 12168–12186. doi:10.1021/acsnano.3c12539.
- Vancouver
- 1.Debruyne A, Okkelman I, Heymans N, Pinheiro C, Hendrix A, Nobis M, et al. Live microscopy of multicellular spheroids with the multimodal near-infrared nanoparticles reveals differences in oxygenation gradients. ACS NANO. 2024;18(19):12168–86.
- IEEE
- [1]A. Debruyne et al., “Live microscopy of multicellular spheroids with the multimodal near-infrared nanoparticles reveals differences in oxygenation gradients,” ACS NANO, vol. 18, no. 19, pp. 12168–12186, 2024.
@article{01HWZB92HHDQZYPR3SNAY6RHZX, abstract = {{Assessment of hypoxia, nutrients, metabolite gradients, and other hallmarks of the tumor microenvironment within 3D multicellular spheroid and organoid models represents a challenging analytical task. Here, we report red/near-infrared (NIR) emitting cell staining with O2-sensitive nanoparticles, which enable measurements of spheroid oxygenation on a conventional fluorescence microscope. Nanosensor probes, termed “MMIR” (multimodal infrared), incorporate an NIR O2-sensitive metalloporphyrin (PtTPTBPF) and deep red aza-BODIPY reference dyes within a biocompatible polymer shell, allowing for oxygen gradient quantification via fluorescence ratio and phosphorescence lifetime readouts. We optimized staining techniques and evaluated the nanosensor probe characteristics and cytotoxicity. Subsequently, we applied nanosensors to the live spheroid models based on HCT116, DPSCs, and SKOV3 cells, at rest, and treated with drugs affecting cell respiration. We found that the growth medium viscosity, spheroid size, and formation method influenced spheroid oxygenation. Some spheroids produced from HCT116 and dental pulp stem cells exhibited “inverted” oxygenation gradients, with higher core oxygen levels than the periphery. This contrasted with the frequently encountered “normal” gradient of hypoxia toward the core caused by diffusion. Further microscopy analysis of spheroids with an “inverted” gradient demonstrated metabolic stratification of cells within spheroids: thus, autofluorescence FLIM of NAD(P)H indicated the formation of a glycolytic core and localization of OxPhos-active cells at the periphery. Collectively, we demonstrate a strong potential of NIR-emitting ratiometric nanosensors for advanced microscopy studies targeting live and quantitative real-time monitoring of cell metabolism and hypoxia in complex 3D tissue models.}}, author = {{Debruyne, Angela and Okkelman, Irina and Heymans, Nina and Pinheiro, Cláudio and Hendrix, An and Nobis, Max and Borisov, Sergey M. and Dmitriev, Ruslan}}, issn = {{1936-0851}}, journal = {{ACS NANO}}, keywords = {{oxygenation,nanoparticles,multicellularspheroids,FLIM,fluorescence microscopy,hypoxia,cancer}}, language = {{eng}}, number = {{19}}, pages = {{12168--12186}}, title = {{Live microscopy of multicellular spheroids with the multimodal near-infrared nanoparticles reveals differences in oxygenation gradients}}, url = {{http://doi.org/10.1021/acsnano.3c12539}}, volume = {{18}}, year = {{2024}}, }
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