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Acute cigarette smoke or extract exposure rapidly activates TRPA1-mediated calcium influx in primary human airway smooth muscle cells

Abstract:
The cystic fibrosis transmembrane conductance regulator (CFTR) anion channel and the epithelial Na+ channel (ENaC) play essential roles in transepithelial ion and fluid transport in numerous epithelial tissues. Inhibitors of both channels have been important tools for defining their physiological role in vitro. However, two commonly used CFTR inhibitors, CFTRinh-172 and GlyH-101, also inhibit non-CFTR anion channels, indicating they are not CFTR specific. However, the potential off-target effects of these inhibitors on epithelial cation channels has to date not been addressed. Here, we show that both CFTR blockers, at concentrations routinely employed by many researchers, caused a significant inhibition of store-operated calcium entry (SOCE) that was time-dependent, poorly reversible and independent of CFTR. Patch clamp experiments showed that both CFTRinh-172 and GlyH-101 caused a significant block of Orai1-mediated whole cell currents, establishing that they likely reduce SOCE via modulation of this Ca2+ release-activated Ca2+ (CRAC) channel. In addition to off-target effects on calcium channels, both inhibitors significantly reduced human αβγ-ENaC-mediated currents after heterologous expression in Xenopus oocytes, but had differential effects on δβγ-ENaC function. Molecular docking identified two putative binding sites in the extracellular domain of ENaC for both CFTR blockers. Together, our results indicate that caution is needed when using these two CFTR inhibitors to dissect the role of CFTR, and potentially ENaC, in physiological processes
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41598-021-89051-4
Publication website:
https://pub.h-brs.de/files/6457/s00424-022-02758-9.pdf

Authors

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-6424-204X
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Role:
Author
ORCID:
0000-0002-9981-2783
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Role:
Author
ORCID:
0000-0003-2885-3382
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Role:
Author
ORCID:
0000-0002-8913-4165
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Role:
Author
ORCID:
0000-0003-4591-8299


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Funder identifier:
10.13039/501100000265
Grant:
MR/M008797/1
More from this funder
Funder identifier:
10.13039/100000002
Grant:
NIH/NHLBI HL135642


Publisher:
Nature Research
Journal:
Scientific Reports More from this journal
Volume:
11
Issue:
1
Pages:
9643-9643
Article number:
9643
Publication date:
2021-05-05
DOI:
EISSN:
2045-2322
ISSN:
2045-2322


Language:
English
Keywords:
Pubs id:
1510170
Local pid:
pubs:1510170
Source identifiers:
W3159840533
Deposit date:
2026-05-12
ARK identifier:
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