Muscarinic Stimulation of Airway Smooth Muscle Cells

1998 ◽  
Vol 31 (3) ◽  
pp. 349-356 ◽  
Author(s):  
Etienne Roux ◽  
Mathieu Molimard ◽  
Savineau ◽  
Roger Marthan
1997 ◽  
Vol 273 (3) ◽  
pp. C868-C873 ◽  
Author(s):  
D. O. Warner ◽  
K. A. Jones ◽  
R. R. Lorenz ◽  
C. M. Pabelick

Prior studies suggest that the mechanism of action by which halothane relaxes airway smooth muscle depends on the contractile state of the cell. We hypothesized that halothane would inhibit the influx of Ca2+ into canine airway smooth muscle cells during submaximal, but not maximal, muscarinic stimulation. This hypothesis was tested by using the rate of quenching of fura 2 fluorescence by Mn2+ in strips of canine tracheal smooth muscle as an index of Ca2+ influx. Acetylcholine (ACh) produced a dose-dependent increase in Mn2+ influx. Halothane (0.64 +/- 0.05 microM) significantly decreased Mn2+ influx and intracellular Ca2+ concentration when added to strips stimulated with a submaximal concentration of ACh (0.3 microM) but had no effect on Mn2+ influx or intracellular Ca2+ concentration during maximal stimulation with ACh (100 microM). Similar results were observed when the strips were treated with verapamil. These results demonstrate that anesthetic effects on Ca2+ homeostasis in intact canine tracheal smooth muscle cells may be critically modulated by receptor-linked mechanisms.


2013 ◽  
Vol 228 (8) ◽  
pp. 1745-1753 ◽  
Author(s):  
Stamatina Tsapournioti ◽  
Ilias Mylonis ◽  
Apostolia Hatziefthimiou ◽  
Maria G. Ioannou ◽  
Rodopi Stamatiou ◽  
...  

2002 ◽  
Vol 282 (1) ◽  
pp. L91-L98 ◽  
Author(s):  
Tracy L. Ediger ◽  
Bryan L. Danforth ◽  
Myron L. Toews

Human airway smooth muscle cells treated with lysophosphatidic acid (LPA) and epidermal growth factor (EGF) exhibit synergistic stimulation of mitogenesis (Ediger TL and Toews ML. J Pharmacol Exp Ther 294: 1076–1082, 2000). The effects of LPA treatment of human airway smooth muscle cells on EGF receptor (EGFR) regulation have now been investigated. LPA treatment for 12–24 h resulted in a twofold increase in 125I-EGF binding and EGFR protein levels as assessed by Western blot analysis. Competition binding assays indicated single-site binding with an affinity of 3 nM, and the affinity was not changed by LPA treatment. EGFR upregulation was blocked by cycloheximide and actinomycin D, suggesting that LPA influences transcriptional regulation of EGFR expression. Inhibitor studies revealed a prominent role for activation of mitogen-activated protein kinase and p70 ribosomal S6 kinase. Both synergism and EGFR upregulation increased with increased cell density, whereas EGFR expression in control cells decreased. The similar requirements for exposure time, LPA concentrations, and cell confluence suggest that EGFR upregulation may be one contributing factor to the synergistic stimulation of mitogenesis seen with LPA plus EGF.


Sign in / Sign up

Export Citation Format

Share Document