Constitutive and evoked release of ATP in adult mouse olfactory epithelium
Affiliation
Department of Physiology, University of ArizonaIssue Date
2024-01-16Keywords
confocal imagingimmunohistochemistry
luciferin-luciferase assay
OP6 cells
primary cell cultures
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Walter de Gruyter GmbHCitation
Hayoz, S., Jia, C. & Hegg, C. (2024). Constitutive and evoked release of ATP in adult mouse olfactory epithelium. Open Life Sciences, 19(1), 20220811. https://doi.org/10.1515/biol-2022-0811Journal
Open Life SciencesRights
© 2024 the author(s), published by De Gruyter. This work is licensed under the Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
In adult olfactory epithelium (OE), ATP plays a role in constant cell turnover and post-injury neuroregeneration. We previously demonstrated that constitutive and ATP-evoked ATP release are present in neonatal mouse OE and underlie continuous cell turn-over and post-injury neuroregeneration, and that activation of purinergic P2X7 receptors is involved in the evoked release. We hypothesized that both releases are present in adult mouse OE. To study the putative contribution of olfactory sensory neurons to ATP release, we used olfactory sensory neuronal-like OP6 cells derived from the embryonic olfactory placode cells. Calcium imaging showed that OP6 cells and primary adult OE cell cultures express functional purinergic receptors. We monitored ATP release from OP6 cells and whole adult OE turbinates using HEK cells as biosensors and luciferin-luciferase assays. Constitutive ATP release occurs in OP6 cells and whole adult mouse OE turbinates, and P2X7 receptors mediated evoked ATP release occurs only in turbinates. The mechanisms of ATP release described in the present study might underlie the constant cell turn-over and post-injury neuroregeneration present in adult OE and thus, further studies of these mechanisms are warranted as it will improve our knowledge of OE tissue homeostasis and post-injury regeneration. © 2024 the author(s), published by De Gruyter.Note
Open access journalISSN
2391-5412Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1515/biol-2022-0811
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Except where otherwise noted, this item's license is described as © 2024 the author(s), published by De Gruyter. This work is licensed under the Creative Commons Attribution 4.0 International License.