Please use this identifier to cite or link to this item:
https://doi.org/10.21256/zhaw-26839
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Vo, Andy N. | - |
dc.contributor.author | Kundu, Srikanya | - |
dc.contributor.author | Strong, Caroline | - |
dc.contributor.author | Jung, Olive | - |
dc.contributor.author | Lee, Emily | - |
dc.contributor.author | Song, Min Jae | - |
dc.contributor.author | Boutin, Molly E. | - |
dc.contributor.author | Raghunath, Michael | - |
dc.contributor.author | Ferrer, Marc | - |
dc.date.accessioned | 2023-02-09T11:36:58Z | - |
dc.date.available | 2023-02-09T11:36:58Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 2073-4409 | de_CH |
dc.identifier.uri | https://digitalcollection.zhaw.ch/handle/11475/26839 | - |
dc.description | Swissnex Austausch | de_CH |
dc.description.abstract | The neuroglial extracellular matrix (ECM) provides critical support and physiological cues for the proper growth, differentiation, and function of neuronal cells in the brain. However, in most in vitro settings that study neural physiology, cells are grown as monolayers on stiff surfaces that maximize adhesion and proliferation, and, therefore, they lack the physiological cues that ECM in native neuronal tissues provides. Macromolecular crowding (MMC) is a biophysical phenomenon based on the principle of excluded volume that can be harnessed to induce native ECM deposition by cells in culture. Here, we show that MMC using two species of Ficoll with vitamin C supplementation significantly boosts deposition of relevant brain ECM by cultured human astrocytes. Dopaminergic neurons cocultured on this astrocyte-ECM bed prepared under MMC treatment showed longer and denser neuronal extensions, a higher number of pre ad post synaptic contacts, and increased physiological activity, as evidenced by higher frequency calcium oscillation, compared to standard coculture conditions. When the pharmacological activity of various compounds was tested on MMC-treated cocultures, their responses were enhanced, and for apomorphine, a D2-receptor agonist, it was inverted in comparison to control cell culture conditions, thus emulating responses observed in in vivo settings. These results indicate that macromolecular crowding can harness the ECM-building potential of human astrocytes in vitro forming an ultra-flat 3D microenvironment that makes neural cultures more physiological and pharmacological relevant. | de_CH |
dc.language.iso | en | de_CH |
dc.publisher | MDPI | de_CH |
dc.relation.ispartof | Cells | de_CH |
dc.rights | http://creativecommons.org/licenses/by/4.0/ | de_CH |
dc.subject | Drug testing | de_CH |
dc.subject | Extracellular matrix | de_CH |
dc.subject | Human iPSC derived astrocyte and dopaminergic neurons | de_CH |
dc.subject | Macromolecular crowding | de_CH |
dc.subject | Cell differentiation | de_CH |
dc.subject | Coculture technique | de_CH |
dc.subject | Humans | de_CH |
dc.subject | Macromolecular substance | de_CH |
dc.subject | Cell culture technique | de_CH |
dc.subject | Extracellular matrix | de_CH |
dc.subject.ddc | 610.28: Biomedizin, Biomedizinische Technik | de_CH |
dc.title | Enhancement of neuroglial extracellular matrix formation and physiological activity of dopaminergic neural cocultures by macromolecular crowding | de_CH |
dc.type | Beitrag in wissenschaftlicher Zeitschrift | de_CH |
dcterms.type | Text | de_CH |
zhaw.departement | Life Sciences und Facility Management | de_CH |
zhaw.organisationalunit | Institut für Chemie und Biotechnologie (ICBT) | de_CH |
dc.identifier.doi | 10.3390/cells11142131 | de_CH |
dc.identifier.doi | 10.21256/zhaw-26839 | - |
dc.identifier.pmid | 35883574 | de_CH |
zhaw.funding.eu | No | de_CH |
zhaw.issue | 14 | de_CH |
zhaw.originated.zhaw | Yes | de_CH |
zhaw.pages.start | 2131 | de_CH |
zhaw.publication.status | publishedVersion | de_CH |
zhaw.volume | 11 | de_CH |
zhaw.publication.review | Peer review (Publikation) | de_CH |
zhaw.webfeed | Metabolic Tissue Engineering | de_CH |
zhaw.author.additional | No | de_CH |
zhaw.display.portrait | Yes | de_CH |
Appears in collections: | Publikationen Life Sciences und Facility Management |
Files in This Item:
File | Description | Size | Format | |
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2022_Vo-etal_Enhancement-neuroglial_extracellular-matrix-formation-macromolecular-crowding _MDPI.pdf | 6.88 MB | Adobe PDF | View/Open |
Show simple item record
Vo, A. N., Kundu, S., Strong, C., Jung, O., Lee, E., Song, M. J., Boutin, M. E., Raghunath, M., & Ferrer, M. (2022). Enhancement of neuroglial extracellular matrix formation and physiological activity of dopaminergic neural cocultures by macromolecular crowding. Cells, 11(14), 2131. https://doi.org/10.3390/cells11142131
Vo, A.N. et al. (2022) ‘Enhancement of neuroglial extracellular matrix formation and physiological activity of dopaminergic neural cocultures by macromolecular crowding’, Cells, 11(14), p. 2131. Available at: https://doi.org/10.3390/cells11142131.
A. N. Vo et al., “Enhancement of neuroglial extracellular matrix formation and physiological activity of dopaminergic neural cocultures by macromolecular crowding,” Cells, vol. 11, no. 14, p. 2131, 2022, doi: 10.3390/cells11142131.
VO, Andy N., Srikanya KUNDU, Caroline STRONG, Olive JUNG, Emily LEE, Min Jae SONG, Molly E. BOUTIN, Michael RAGHUNATH und Marc FERRER, 2022. Enhancement of neuroglial extracellular matrix formation and physiological activity of dopaminergic neural cocultures by macromolecular crowding. Cells. 2022. Bd. 11, Nr. 14, S. 2131. DOI 10.3390/cells11142131
Vo, Andy N., Srikanya Kundu, Caroline Strong, Olive Jung, Emily Lee, Min Jae Song, Molly E. Boutin, Michael Raghunath, and Marc Ferrer. 2022. “Enhancement of Neuroglial Extracellular Matrix Formation and Physiological Activity of Dopaminergic Neural Cocultures by Macromolecular Crowding.” Cells 11 (14): 2131. https://doi.org/10.3390/cells11142131.
Vo, Andy N., et al. “Enhancement of Neuroglial Extracellular Matrix Formation and Physiological Activity of Dopaminergic Neural Cocultures by Macromolecular Crowding.” Cells, vol. 11, no. 14, 2022, p. 2131, https://doi.org/10.3390/cells11142131.
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