Oxygen sensing by ion channels and chemotransduction in single glomus cells

Journal of General Physiology

Volumn 107, Issue 1, 1996, Pages 133-143

  Montoro, R J ^a   Urena J ^a   Fernandez Chacon R ^a   Alvarez De Toledo, G ^a   Lopez Barneo J ^a  

^a UNIVERSITY OF SEVILLE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; DOPAMINE; ION CHANNEL; OXYGEN; POTASSIUM ION;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM CURRENT; CAROTID BODY; CELL HYPOXIA; CHEMOSENSITIVITY; CONTROLLED STUDY; NONHUMAN; OXYGEN TENSION; RABBIT;

ACTION POTENTIALS; ANIMALS; CALCIUM; CAROTID BODY; DOPAMINE; ION CHANNELS; OXYGEN; RABBITS; SIGNAL TRANSDUCTION;

EID: 0030045380     PISSN: 00221295     EISSN: None     Source Type: Journal    
DOI: 10.1085/jgp.107.1.133     Document Type: Article

References (41)

1. 2+ signal from fura-2 loaded mast cells depends strongly on the method of dye loading. FEBS Lett. 192:13-18.
2. Alvarez de Toledo, G., R. Fernández-Chacón, and J. Fernández. 1993. Release of secretory products during transient vesicle fusion. Nature (Land.). 363:554-557.
3. Biscoe, T. J., and M. R. Duchen. 1990. Cellular basis of transduction in carotid chemoreceptors. Am. J. Physiol. 258:L271-L27S.
4. Biscoe, T. J., M. J. Purves, and S. R. Sampson. 1970. The frequency of nerve impulses in single carotid body chemoreceptor afferent fibers recorded in vivo with intact circulation. J. Physiol (Land.). 208:121-131.
5. Buckler, K.J., and R. D. Vaughan-Jones. 1994. Effects of hypoxia on membrane potential and intracellular calcium in rat neonatal carotid body type I cells. J. Physiol. (Land.). 476:423-428.
6. 2+ and the secretory-vesicle dynamics. Trends Neurosa. 18:191-196.
7. Chow, R. H., L. von Rüden, and E. Neher. 1992. Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells Nature (Land.). 356:60-63.
8. + channel in type-I cell of the rabbit carotid body. FEBS Lett. 249:195-198.
9. Donnelly, D. F. 1993. Electrochemical detection of catecholamine release from rat carotid body in vitro. J. Appl. Physiol. 74:2330-2337.
10. Duchen, M. R., K. W. T. Caddv, G. C. Kirby, D. L. Patterson, J. Ponte, and T. J. Biscoe. 1988. Biophysical studies of the cellular elements of the rabbit carotid body. Neuroicience. 26:291-311.
11. Fenwick. E. M., A. Marty, and E. Neher. 1982. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetvlcholine. J. Physiol. (Lond.). 331:577-597.
12. Fidone, S. J., and C. González. 1986. Initiadon and control of chemoreceptor activity in the carotid body. In Handbook of Physiology. The Respiratory System. Vol. II. A. P Fishman, editor. American Physiological Society, MD. 247-312.
13. Fishman, M. C., W. L. Greene, and D. Platika. 1985. Oxygen chemoreception by carotid body cells in culture. Proc. Natl. Acad. Sci. USA. 82:1448-1450.
14. Franco-Obregón, A., J. Ureña, and J. López-Barnco. 1995. Oxygen-sensitive calcium channels in vascular smooth muscle and their possible role in hypoxic arterial relaxation. Pror. Natl. Acad. Sci., USA. 92:4715-4719.
15. 2 tension. Proc. Natl. Acad. Sci., USA. 88:2927-2930.
16. Ganfornina, M. D., and J. López-Barneo. 1992a. Potassium channel types in arterial chemoreceptor cells and their selective modulation by oxygen. J. Gen. Physiol. 100:401-426.
17. 2 J. Gen. Physiol. 100:427-455.
18. González, C., L. Almaraz. A. Obeso. and R. Rigual. 1992. Oxygen and acid chemoreception in the carotid body chemoreceptors. Trends Neurosci. 15:146-153.
19. Grynkiewicz, G., M. Poenie, and R. Y. Tsien. 1985. A new generation of Ca indicators with greatly improved fluorescence properties. J. Biol. Chem. 260:3440-3450.
20. Hamill, O. P., A. Martv, E. Neher, B. Sakmann, and F. Sigworth, 1981. Improved patch clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 391:85-100.
21. Heidelberger, R., C. Heinemann. E. Neher, and G. Matthews. 1994. Calcium dependence of the rate of exocytosis in a synaptic terminal. Nature (Lond.). 371:513-515.
22. Hornbein, T. F. 1968. The relationship between stimulus to chemoreceptors and their response. In Arterial Chemoreceptors. R. W. Torrance. editor. Blackwell, Oxford. 65-78.
23. 2 chemoreception: the carotid body model. News Physiol. Sci. 9:161-165.
24. 2 in the cat carotid body chemotransduction. J. Appl. Physiol. 75:1035-1043.
25. López-Barneo, J. 1994. Oxygen-sensitive ion channels: how ubiquitous are they? Trends Neurosci. 17:133-135.
26. López-Barneo, J., A. R. Benot, and J. Ureña. 1993. Oxygen sensing and the electrophysiology of arterial chemoreceptor cells. News Physiol, Sci. 8:191-195.
27. 2 in type I chemoreceptor cells. Science (Wash. DC). 242:580-582.
28. + channel activity in chemoreceptor cells of the mammalian carotid body. J. Gen. Physiol. 93: 1001-1015.
29. McDonald, D. M. 1981. Peripheral chemoreceptors: structure-function relationships in the carotid body. In Regulation of Breathing. T. R Hornbein. editor. Marcel Dekker, New York. 105-320.
30. Montoro, R., and J. López-Barneo. 1995. Calcium channels in glomus cells and their regulation by oxygen tension. Biophys. J. 68:A209.
31. + current. Neurosci Lett. 119:253-256.
32. 2+ elevation above a threshold level in bullfrog sympathetic ganglia, Neuron. 10:465-473.
33. Rigual, R., E. González, C. González, and S. Fidone. 1986. Synthesis and release of catecholamines by the cat carotid body in vitro: effect of hypoxic stimulation. Brain Res. 374:101-109.
34. Sato, M., K. Ikeda, K. Yoshizaki, and H. Koyano. 1991. Response of cytosolic calcium to anoxia and cyanide in cultured glomus cells of new born rabbit carotid body. Brain Res. 551:327-330.
35. 2-sensitive rat carotid body cells grown in short-and long-term culture. Pflugers Arch. 418:93-101.
36. 2+ receptor controls the final steps in peptide secretion from pituitary melanotrophs. Neuron. 11:93-104.
37. 2+ by the peptide TRH and its derivatives in guinea-pig septal neurones. J. Physiol. (Loand.). 472:327-340.
38. 2+ entry and quantal dopamine secretion in carotid body glomus cells. Proc. Natl. Acad. Sci., USA. 91:10208-10211.
39. Ureña, J., J. R. López-López, C. González, and J. López-Barneo. 1989. Ionic currents in dispersed chemoreceptor cells of the mammalian carotid body. J. Gen. Physiol. 93:979-999.
40. Verna, A., M. Roumy, and L. M. Leitner. 1975. Loss of chemoreceptive properties of the rabbit carotid body after destruction of the glomus cells. Brain Res. 100:13-23.
41. Wightman, R. M., J. A. Jankowski. R. T. Kennedy, K. T. Kawagoe, T. J. Schroeder, D. J. Leszczyszyn, J. A. Near, E. J. Diliberto, and O. H. Viveros. 1991. Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells. Proc Natl. Acad. Sci., USA. 88:10754-10758.