Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion

Non-olfactory cells have excellent biosensor potential because they express functional olfactory receptors (ORs) and are non-neuronal cells that are easy to culture. ORs are G-protein coupled receptors (GPCRs), and there is a well-established link between different classes of G-proteins and cytoskel...

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Main Authors: Theresa M. Curtis, Annabella M. Nilon, Anthony J. Greenberg, Matthew Besner, Jacob J. Scibek, Jennifer A. Nichols, Janet L. Huie
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Biosensors
Subjects:
Online Access:https://www.mdpi.com/2079-6374/13/3/329
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author Theresa M. Curtis
Annabella M. Nilon
Anthony J. Greenberg
Matthew Besner
Jacob J. Scibek
Jennifer A. Nichols
Janet L. Huie
author_facet Theresa M. Curtis
Annabella M. Nilon
Anthony J. Greenberg
Matthew Besner
Jacob J. Scibek
Jennifer A. Nichols
Janet L. Huie
author_sort Theresa M. Curtis
collection DOAJ
description Non-olfactory cells have excellent biosensor potential because they express functional olfactory receptors (ORs) and are non-neuronal cells that are easy to culture. ORs are G-protein coupled receptors (GPCRs), and there is a well-established link between different classes of G-proteins and cytoskeletal structure changes affecting cellular morphology that has been unexplored for odorant sensing. Thus, the present study was conducted to determine if odorant binding in non-olfactory cells causes cytoskeletal changes that will lead to cell changes detectable by electric cell-substrate impedance sensing (ECIS). To this end, we used the human umbilical vein endothelial cells (HUVECs), which express OR10J5, and the human keratinocyte (HaCaT) cells, which express OR2AT4. Using these two different cell barriers, we showed that odorant addition, lyral and Sandalore, respectively, caused an increase in cAMP, changes in the organization of the cytoskeleton, and a decrease in the integrity of the junctions between the cells, causing a decrease in cellular electrical resistance. In addition, the random cellular movement of the monolayers (micromotion) was significantly decreased after odorant exposure. Collectively, these data demonstrate a new physiological role of olfactory receptor signaling in endothelial and epithelial cell barriers and represent a new label-free method to detect odorant binding.
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spelling doaj.art-6bc71f42e0f04b68ade0ec198ae38e702023-11-17T09:53:50ZengMDPI AGBiosensors2079-63742023-02-0113332910.3390/bios13030329Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and MicromotionTheresa M. Curtis0Annabella M. Nilon1Anthony J. Greenberg2Matthew Besner3Jacob J. Scibek4Jennifer A. Nichols5Janet L. Huie6Department of Biological Sciences, SUNY Cortland, Cortland, NY 13045, USADepartment of Biological Sciences, SUNY Cortland, Cortland, NY 13045, USABayesic Research, LLC, Ithaca, NY 14850, USADepartment of Biological Sciences, SUNY Cortland, Cortland, NY 13045, USADepartment of Biological Sciences, SUNY Cortland, Cortland, NY 13045, USAJan Biotech, Inc., Ithaca, NY 14850, USAJan Biotech, Inc., Ithaca, NY 14850, USANon-olfactory cells have excellent biosensor potential because they express functional olfactory receptors (ORs) and are non-neuronal cells that are easy to culture. ORs are G-protein coupled receptors (GPCRs), and there is a well-established link between different classes of G-proteins and cytoskeletal structure changes affecting cellular morphology that has been unexplored for odorant sensing. Thus, the present study was conducted to determine if odorant binding in non-olfactory cells causes cytoskeletal changes that will lead to cell changes detectable by electric cell-substrate impedance sensing (ECIS). To this end, we used the human umbilical vein endothelial cells (HUVECs), which express OR10J5, and the human keratinocyte (HaCaT) cells, which express OR2AT4. Using these two different cell barriers, we showed that odorant addition, lyral and Sandalore, respectively, caused an increase in cAMP, changes in the organization of the cytoskeleton, and a decrease in the integrity of the junctions between the cells, causing a decrease in cellular electrical resistance. In addition, the random cellular movement of the monolayers (micromotion) was significantly decreased after odorant exposure. Collectively, these data demonstrate a new physiological role of olfactory receptor signaling in endothelial and epithelial cell barriers and represent a new label-free method to detect odorant binding.https://www.mdpi.com/2079-6374/13/3/329odorant cell-based biosensorelectrical resistancemicromotioncytoskeletonolfactory receptorbarrier function
spellingShingle Theresa M. Curtis
Annabella M. Nilon
Anthony J. Greenberg
Matthew Besner
Jacob J. Scibek
Jennifer A. Nichols
Janet L. Huie
Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
Biosensors
odorant cell-based biosensor
electrical resistance
micromotion
cytoskeleton
olfactory receptor
barrier function
title Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
title_full Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
title_fullStr Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
title_full_unstemmed Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
title_short Odorant Binding Causes Cytoskeletal Rearrangement, Leading to Detectable Changes in Endothelial and Epithelial Barrier Function and Micromotion
title_sort odorant binding causes cytoskeletal rearrangement leading to detectable changes in endothelial and epithelial barrier function and micromotion
topic odorant cell-based biosensor
electrical resistance
micromotion
cytoskeleton
olfactory receptor
barrier function
url https://www.mdpi.com/2079-6374/13/3/329
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