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P2X4 and nNOS expression in human ciliated airway epithelium

P2X4 and nNOS expression in human ciliated airway epithelium
P2X4 and nNOS expression in human ciliated airway epithelium
Background Calcium (Ca2+) and nitric oxide (NO) modulate ciliary beat frequency (CBF). NO synthase (NOS) isoenzymes, responsible for NO production, localise in human airway epithelium and constitutive NOS activity is dependant on Ca2+. Adenosine triphosphate gated purinergic ion channels, comprised of P2X1–7 subunits, govern Ca2+ influx and P2X4 reportedly localises to rabbit airway cilia. Also, P2X proteins co-localise with neuronal NOS (nNOS) in guinea pig cochlea outer hair cells and rat hypothalamus. We hypothesised that P2X4 and nNOS co-localise in human airway cilia and are involved in modulating CBF.

Objectives To determine P2X1,3–7 mRNA expression and P2X4 and nNOS localisation in human nasal epithelium, and assess their possible interaction in CBF modulation.

Methods and Results Relative to b-actin expression, consistent and moderate P2X4,6 mRNA and variable P2X3,5,7 mRNA were detected by RT-PCR in (n=4) human primary airway epithelium cultured at air-liquid interface (ALI). In ALI cultured primary epithelium P2X4 localised (n=3) to cell membranes and cytoplasm and nNOS localised to cilia (n=3) by immunofluorescence. P2X4 localised to the ciliary tips (n=2), whilst nNOS localised to the proximal portion of cilia (specificity confirmed by blocking peptide) in nasal polyp paraffin wax sections by immunohistochemistry (n=6). High speed video microscopy confirmed a 30 minute baseline CBF at 37oC (12.9 Hz SD±0.8, n=5) on nasal epithelium biopsies (n=2) and 30 minutes of NOS inhibition [with 1 mM: L-N-Ornithine, 1400W and S-Methyl-L-thiocitrulline] reduced baseline CBF by 20% to 9.6 Hz SD±0.9 (p<0.001) but the P2X4 inhibitor [10 µM brilliant blue G] had no effect.

Conclusion P2X4 and nNOS are expressed in human airway cilia but do not co-localise. NOS inhibition reduced CBF whilst P2X4 inhibition did not, suggesting that blocking P2X4 activity alone is not sufficient to modify NOS activity or CBF .
0040-6376
176-177
Premadeva, Irnthu
1fc18967-7bf1-4511-8411-fdf19c8d5b03
Lenartowicz, H.
dd180956-ad9e-4c44-807a-5263fc987273
Underwood, J.
5fa2bb90-acb2-478c-a499-d110198440a6
Lackie, Peter
4afbbe1a-22a6-4ceb-8cad-f3696dc43a7a
Lucas, Jane
5cb3546c-87b2-4e59-af48-402076e25313
Jackson, Claire
64cdd6fa-74c3-4ac6-94ef-070620a6efd9
Premadeva, Irnthu
1fc18967-7bf1-4511-8411-fdf19c8d5b03
Lenartowicz, H.
dd180956-ad9e-4c44-807a-5263fc987273
Underwood, J.
5fa2bb90-acb2-478c-a499-d110198440a6
Lackie, Peter
4afbbe1a-22a6-4ceb-8cad-f3696dc43a7a
Lucas, Jane
5cb3546c-87b2-4e59-af48-402076e25313
Jackson, Claire
64cdd6fa-74c3-4ac6-94ef-070620a6efd9

Premadeva, Irnthu, Lenartowicz, H., Underwood, J., Lackie, Peter, Lucas, Jane and Jackson, Claire (2012) P2X4 and nNOS expression in human ciliated airway epithelium. Thorax, 67 (Suppl 2), 176-177. (doi:10.1136/thoraxjnl-2012-202678.348).

Record type: Meeting abstract

Abstract

Background Calcium (Ca2+) and nitric oxide (NO) modulate ciliary beat frequency (CBF). NO synthase (NOS) isoenzymes, responsible for NO production, localise in human airway epithelium and constitutive NOS activity is dependant on Ca2+. Adenosine triphosphate gated purinergic ion channels, comprised of P2X1–7 subunits, govern Ca2+ influx and P2X4 reportedly localises to rabbit airway cilia. Also, P2X proteins co-localise with neuronal NOS (nNOS) in guinea pig cochlea outer hair cells and rat hypothalamus. We hypothesised that P2X4 and nNOS co-localise in human airway cilia and are involved in modulating CBF.

Objectives To determine P2X1,3–7 mRNA expression and P2X4 and nNOS localisation in human nasal epithelium, and assess their possible interaction in CBF modulation.

Methods and Results Relative to b-actin expression, consistent and moderate P2X4,6 mRNA and variable P2X3,5,7 mRNA were detected by RT-PCR in (n=4) human primary airway epithelium cultured at air-liquid interface (ALI). In ALI cultured primary epithelium P2X4 localised (n=3) to cell membranes and cytoplasm and nNOS localised to cilia (n=3) by immunofluorescence. P2X4 localised to the ciliary tips (n=2), whilst nNOS localised to the proximal portion of cilia (specificity confirmed by blocking peptide) in nasal polyp paraffin wax sections by immunohistochemistry (n=6). High speed video microscopy confirmed a 30 minute baseline CBF at 37oC (12.9 Hz SD±0.8, n=5) on nasal epithelium biopsies (n=2) and 30 minutes of NOS inhibition [with 1 mM: L-N-Ornithine, 1400W and S-Methyl-L-thiocitrulline] reduced baseline CBF by 20% to 9.6 Hz SD±0.9 (p<0.001) but the P2X4 inhibitor [10 µM brilliant blue G] had no effect.

Conclusion P2X4 and nNOS are expressed in human airway cilia but do not co-localise. NOS inhibition reduced CBF whilst P2X4 inhibition did not, suggesting that blocking P2X4 activity alone is not sufficient to modify NOS activity or CBF .

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Published date: 19 November 2012

Identifiers

Local EPrints ID: 470023
URI: http://eprints.soton.ac.uk/id/eprint/470023
ISSN: 0040-6376
PURE UUID: 08d52729-6943-467b-855a-189b9606489c
ORCID for Peter Lackie: ORCID iD orcid.org/0000-0001-7138-3764
ORCID for Jane Lucas: ORCID iD orcid.org/0000-0001-8701-9975
ORCID for Claire Jackson: ORCID iD orcid.org/0000-0002-1200-0935

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Date deposited: 30 Sep 2022 16:42
Last modified: 17 Mar 2024 03:02

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Contributors

Author: Irnthu Premadeva
Author: H. Lenartowicz
Author: J. Underwood
Author: Peter Lackie ORCID iD
Author: Jane Lucas ORCID iD
Author: Claire Jackson ORCID iD

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