Gas-modulating microcapsules for spatiotemporal control of hypoxia
Molley, Thomas G., Jiang, Shouyuan, Ong, Louis, Kopecky, Chantal, Ranaweera, Chavinya D., Jalandhra, Gagan K., Milton, Laura, Kardia, Egi, Zhou, Zeheng, Rnjak-Kovacina, Jelena, Waters, Shafagh A., Toh, Yi Chin, & Kilian, Kristopher A. (2023) Gas-modulating microcapsules for spatiotemporal control of hypoxia. Proceedings of the National Academy of Sciences of the United States of America, 120(16), Article number: e2217557120.
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130380759. Available under License Creative Commons Attribution Non-commercial No Derivatives 4.0. |
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Description
Oxygen is a vital molecule involved in regulating development, homeostasis, and disease. The oxygen levels in tissue vary from 1 to 14% with deviations from homeostasis impacting regulation of various physiological processes. In this work, we developed an approach to encapsulate enzymes at high loading capacity, which precisely controls the oxygen content in cell culture. Here, a single microcapsule is able to locally perturb the oxygen balance, and varying the concentration and distribution of matrix-embedded microcapsules provides spatiotemporal control. We demonstrate attenuation of hypoxia signaling in populations of stem cells, cancer cells, endothelial cells, cancer spheroids, and intestinal organoids. Varying capsule placement, media formulation, and timing of replenishment yields tunable oxygen gradients, with concurrent spatial growth and morphogenesis in a single well. Capsule containing hydrogel films applied to chick chorioallantoic membranes encourages neovascularization, providing scope for topical treatments or hydrogel wound dressings. This platform can be used in a variety of formats, including deposition in hydrogels, as granular solids for 3D bioprinting, and as injectable biomaterials. Overall, this platform's simplicity and flexibility will prove useful for fundamental studies of oxygen-mediated processes in virtually any in vitro or in vivo format, with scope for inclusion in biomedical materials for treating injury or disease.
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| ID Code: | 239258 | ||
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| Item Type: | Contribution to Journal (Journal Article) | ||
| Refereed: | Yes | ||
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| Additional Information: | Acknowledgments: This work was supported through funding from the National Health and Medical Research Council (K.A.K.: APP1185021; S.A.W.: APP1188987), the Australian Research Council (K.A.K.: DP210103654; Y.-C.T.: FT180100157 and DP200101658), and the National Cancer Institute of the NIH grant (K.A.K.: R01CA251443). Portions of this paper were developed from the thesis of T.G.M. We acknowledge the help and support of staff at the Katharina Gaus Light Microscopy Facility and the Biological Specimen Preparation Laboratory of the University of New South Wales (UNSW) Mark Wainwright Analytical Centre. | ||
| Measurements or Duration: | 12 pages | ||
| Keywords: | biomaterials, cancer, hypoxia, microcapsules, stem cells, MPQC | ||
| DOI: | 10.1073/pnas.2217557120 | ||
| ISSN: | 0027-8424 | ||
| Pure ID: | 130380759 | ||
| Divisions: | Current > Research Centres > Centre for Biomedical Technologies Current > Research Centres > Centre for Microbiome Research Current > QUT Faculties and Divisions > Faculty of Engineering Current > Schools > School of Mechanical, Medical & Process Engineering Current > QUT Faculties and Divisions > Faculty of Health |
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| Funding Information: | ACKNOWLEDGMENTS. This work was supported through funding from the National Health and Medical Research Council (K.A.K.: APP1185021; S.A.W.: APP1188987), the Australian Research Council (K.A.K.: DP210103654; Y.-C.T.: FT180100157 and DP200101658), and the National Cancer Institute of the NIH grant (K.A.K.: R01CA251443). Portions of this paper were developed from the thesis of T.G.M. We acknowledge the help and support of staff at the Katharina Gaus Light Microscopy Facility and the Biological Specimen This work was supported through funding from the National Health and Medical Research Council (K.A.K.: APP1185021; S.A.W.: APP1188987), the Australian Research Council (K.A.K.: DP210103654; Y.-C.T.: FT180100157 and DP200101658), and the National Cancer Institute of the NIH grant (K.A.K.: R01CA251443). Portions of this paper were developed from the thesis of T.G.M. We acknowledge the help and support of staff at the Katharina Gaus Light Microscopy Facility and the Biological Specimen Preparation Laboratory of the University of New South Wales (UNSW) Mark Wainwright Analytical Centre. | ||
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| Copyright Owner: | 2023 The Author(s) | ||
| Copyright Statement: | This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au | ||
| Deposited On: | 20 Apr 2023 10:40 | ||
| Last Modified: | 23 Jun 2026 06:58 |
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