Coupling of Airway Smooth Muscle Bitter Taste Receptors to Intracellular Signaling and Relaxation Is via G_αi1,2,3

Authors

Donghwa Kim, University of South FloridaFollow
Jung A. Woo, University of South FloridaFollow
Ezekiel Geffken, Johns Hopkins Bloomberg School of Public Health
Steven S. An, Johns Hopkins Bloomberg School of Public Health
Stephen B. Liggett, University of South FloridaFollow

Document Type

Article

Publication Date

2016

Keywords

bitter taste receptors, G proteins, airway smooth muscle, asthma, chronic obstructive pulmonary disease Clinical R

Digital Object Identifier (DOI)

https://doi.org/10.1165/rcmb.2016-0373OC

Abstract

Bitter taste receptors (TAS2Rs) are expressed on human airway smooth muscle (HASM) and evoke marked relaxation. Agonist interaction with TAS2Rs activates phospholipase C and increases compartmentalized intracellular Ca2+ ([Ca2+]i) via inositol 1,4,5 triphosphate. In taste cells, the G protein gustducin couples TAS2R to phospholipase C; however, we find very low levels of Gαgust mRNA or protein in HASM. We hypothesized that another G protein in HASM transmits TAS2R function. TAS2R signaling to [Ca2+]i, extracellular signal–regulated kinase (ERK) 1/2, and physiologic relaxation was sensitive to pertussis toxin, confirming a role for a member of the Gi family. α subunit expression in HASM was Gαi2 > Gαi1 = Gαi3 > Gαtrans1 ≈ Gαtrans2, with Gαgust and Gαo at the limits of detection (>100-fold lower than Gαi2). Small interfering RNA knockdowns in HASM showed losses of [Ca2+]i and ERK1/2 signaling when Gαi1, Gαi2, or Gαi3 were reduced. Gαtrans1 and Gαtrans2 knockdowns had no effect on [Ca2+]i and a minimal, transient effect on ERK1/2 phosphorylation. Furthermore, Gαgust and Gαo knockdowns did not affect any TAS2R signaling. In overexpression experiments in human embryonic kidney-293T cells, we confirmed an agonist-dependent physical interaction between TAS2R14 and Gαi2. ASM cells from transgenic mice expressing a peptide inhibitor of Gαi2 had attenuated relaxation to TAS2R agonist. These data indicate that, unlike in taste cells, TAS2Rs couple to the prevalent G proteins, Gαi1, Gαi2, and Gαi3, with no evidence for functional coupling to Gαgust. This absence of function for the “canonical” TAS2R G protein in HASM may be due to the very low expression of Gαgust, indicating that TAS2Rs can optionally couple to several G proteins in a cell type–dependent manner contingent upon G protein expression.

Was this content written or created while at USF?

Yes

Citation / Publisher Attribution

American Journal of Respiratory Cell and Molecular Biology, v. 56, issue 6, p. 762-771

Scholar Commons Citation

Kim, Donghwa; Woo, Jung A.; Geffken, Ezekiel; An, Steven S.; and Liggett, Stephen B., "Coupling of Airway Smooth Muscle Bitter Taste Receptors to Intracellular Signaling and Relaxation Is via G_αi1,2,3" (2016). Internal Medicine Faculty Publications. 229.
https://digitalcommons.usf.edu/intmed_facpub/229