» Articles » PMID: 7756536

Extracellular ATP Induces Hyperpolarization and Motility Stimulation of Ciliary Cells

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1995 Mar 1
PMID 7756536
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Cellular membrane potential and ciliary motility were examined in tissues cultures prepared from frog palate and esophagus epithelia. Addition of micromolar concentrations of extracellular ATP caused membrane hyperpolarization and enhanced the beat frequency. These two effects of ATP were 1) dose dependent, reaching a maximum at 10 microM ATP; 2) dependent on the presence of extracellular Ca2+ or Mg2+; 3) insensitive to inhibitors of voltage-gated calcium channels; 4) abolished after depleting the intracellular Ca2+ stores with thapsigargin; 5) attenuated by quinidine (1 mM), Cs+ (5-20 mM), and replacement of extracellular Na+ by K+; 6) insensitive to charybdotoxin (5-20 nM), TEA (1-20 microM), and apamin (0.1-1 microM); 7) independent of initial membrane potential; and 8) unaffected by amiloride. In addition, extracellular ATP induced an appreciable rise in intracellular Ca2+. Addition of thapsigargin caused an initial enhancement of the ciliary beat frequency and membrane hyperpolarization. These results strongly suggest the involvement of calcium-dependent potassium channels in the response to ATP. The results show that moderate hyperpolarization is closely associated with a sustained enhancement of ciliary beating by extracellular ATP.

Citing Articles

The Interplay between Mitochondrial Metabolism and Nasal Mucociliary Function as a Surrogate Method to Diagnose Thyroid Dysfunction: Insights from a Population-Based Study.

Farhadi M, Ghanbari H, Salehi A, Ashique S, Taghizadeh-Hesary F Biomedicines. 2024; 12(8).

PMID: 39200361 PMC: 11351756. DOI: 10.3390/biomedicines12081897.


Seeing cilia: imaging modalities for ciliary motion and clinical connections.

Peabody J, Shei R, Bermingham B, Phillips S, Turner B, Rowe S Am J Physiol Lung Cell Mol Physiol. 2018; 314(6):L909-L921.

PMID: 29493257 PMC: 6032069. DOI: 10.1152/ajplung.00556.2017.


Drug-induced ciliogenesis in pancreatic cancer cells is facilitated by the secreted ATP-purinergic receptor signaling pathway.

Khan N, Garg A, Agostinis P, Swinnen J Oncotarget. 2018; 9(3):3507-3518.

PMID: 29423062 PMC: 5790479. DOI: 10.18632/oncotarget.23335.


Innervation of Gill Lateral Cells in the Bivalve Mollusc Affects Cellular Membrane Potential and Cilia Activity.

Catapane E, Nelson M, Adams T, Carroll M J Pharmacol Rep. 2016; 1(2).

PMID: 27489887 PMC: 4968879.


Purinergic signalling in the gastrointestinal tract and related organs in health and disease.

Burnstock G Purinergic Signal. 2013; 10(1):3-50.

PMID: 24307520 PMC: 3944042. DOI: 10.1007/s11302-013-9397-9.


References
1.
Eshel D, Priel Z . Characterization of metachronal wave of beating cilia on frog's palate epithelium in tissue culture. J Physiol. 1987; 388:1-8. PMC: 1192531. DOI: 10.1113/jphysiol.1987.sp016597. View

2.
Inoue R, Brading A . The properties of the ATP-induced depolarization and current in single cells isolated from the guinea-pig urinary bladder. Br J Pharmacol. 1990; 100(3):619-25. PMC: 1917811. DOI: 10.1111/j.1476-5381.1990.tb15856.x. View

3.
Wiener E, Dubyak G, Scarpa A . Na+/H+ exchange in Ehrlich ascites tumor cells. Regulation by extracellular ATP and 12-O-tetradecanoylphorbol 13-acetate. J Biol Chem. 1986; 261(10):4529-34. View

4.
Soltoff S, McMillian M, Talamo B . ATP activates a cation-permeable pathway in rat parotid acinar cells. Am J Physiol. 1992; 262(4 Pt 1):C934-40. DOI: 10.1152/ajpcell.1992.262.4.C934. View

5.
Nelson D, Wright E . The distribution, activity, and function of the cilia in the frog brain. J Physiol. 1974; 243(1):63-78. PMC: 1330689. DOI: 10.1113/jphysiol.1974.sp010742. View