Blockade of a retinal cGMP-gated channel by polyamines

Journal of General Physiology

Volumn 113, Issue 1, 1999, Pages 35-43

  Lu, Zhe ^a   Ding, Long ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Cyclic nucleotide gated channel ion permeation; Putrescine; Spermidine; Spermine

Indexed keywords

CALCIUM ION; CYCLIC GMP; MAGNESIUM ION; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; POLYAMINE; PUTRESCINE; SPERMIDINE; SPERMINE;

ANIMAL CELL; ARTICLE; CATTLE; CELL MEMBRANE CONDUCTANCE; CELL MEMBRANE DEPOLARIZATION; CELL MEMBRANE POTENTIAL; CHANNEL GATING; CONTROLLED STUDY; NOISE; NONHUMAN; OOCYTE; RETINA ROD; SIGNAL TRANSDUCTION; XENOPUS LAEVIS;

ANIMALS; CATTLE; CYCLIC GMP; ELECTRIC STIMULATION; ELECTROPHYSIOLOGY; EXTRACELLULAR SPACE; ION CHANNEL GATING; LIGHT; MEMBRANE POTENTIALS; PATCH-CLAMP TECHNIQUES; POLYAMINES; RETINA; RODS (RETINA);

EID: 0032916347     PISSN: 00221295     EISSN: None     Source Type: Journal    
DOI: 10.1085/jgp.113.1.35     Document Type: Article

References (50)

1. Araneda, R.C., R.S. Zukin, and M.V.L. Bennett. 1993. Effects of polyamines on NMDA-induced currents in rat hippocampal neurons: a whole-cell and single channel study. Neurosci. Lett. 152: 107-112.
2. Ault, B., R.H. Evans, A.A. Francis, D.J. Oakes, and J.C. Witkins. 1980. Selective depression of excitatory amino acid induced depolarization by magnesium ions in isolated spinal cord preparations. J. Physiol 307:413-428.
3. Bader, C.R., P.R. Macleish, and E.A. Schwartz. 1979. A voltage-clamp study of the light response in solitary rods of the tiger salamander. J. Physiol. (Camb.). 296:1-26.
4. Bahring, R., D. Boeie, M. Benveniste, and M.L. Mayer. 1997. Permeation and block of the rat GluR6 glutamate receptor channels by internal and external polyamines. J. Physiol. (Camb.). 502: 575-589.
5. Bastian, B.L., and G.L. Fein. 1982. The effects of sodium replacement on the responses of toad rads. J. Physiol. (Camb.). 330:331-347.
6. Baylor, D.A., and B.J. Nunn. 1986. Electrical properties of the light-sensitive conductance of salamander rods. J. Physiol. (Camb.). 371: 115-145.
7. Benveniste, M., and M.L. Mayer. 1993. Multiple effects of spermine on N-methyl-D-aspartic acid receptor responses of rat cultured hippocampal neurons. J. Physiol. (Camb.). 464:131-163.
8. Bododia, R.D., and P.B. Detwiler. 1985. Patch-clamp recordings of the light-sensitive dark noise in retinal rods from the lizard and frog. J. Physiol. (Camb.). 367:183-216.
9. Bowie, D., and M.L. Mayer. 1995. Inward rectification of both AMPA and kainate subtype glutamate receptors generated by polyamine-mediated ion channel block. Neuron. 15:453-462.
10. Capovilla, M., A. Caretta, L. Cervetto, and V. Torre. 1983. Ionic movements through light-sensitive channels of toad rods. J. Physiol. (Camb.). 343:295-310.
11. 1-(n-octane-sulfonyl)-spermine, novel glutamate receptor antagonists: block and permeation of N-methyl-D-aspartate receptors. Mol. Pharmacol. 51:861-871.
12. Colamartino, G., A. Menini, and V. Torre. 1991. Blockade and permeation of divalent cations through the cyclic GMP-activated channel from tiger salamander retinal rods. J. Physiol. (Camb.). 440:189-206.
13. 2+-permeable-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid receptors. Proc. Natl. Acad. Sci. USA. 92:9298-9302.
14. 2+ blockage, and ion selectivity. Proc. Natl. Acad. Sci. USA. 91: 1109-1113.
15. + channels is caused by intracellular spermine. Cell. 80:149-154.
16. + channels. Science. 266:1068-1072.
17. Golliding, E.H., J. Ngai, R.H. Kramer, S. Colicos, R. Axel, S.A. Siegelbaum, and A. Chess. 1992. Molecular cloning and single channel properties of the cyclic nucleotide-gated channel from catfish olfactory neurons. Neuron. 8:45-58.
18. Goulding, E.H., G.R. Tibbs, D. Liu, and S.A. Siegelbaum. 1993. Role of H5 domain in determining pore diameter and ion permeation through cyclic nucleotide-gated channels. Nature. 364: 61-64.
19. Haynes, L.W., A.R. Kay, and K.-W. Yau. 1986. Single cyclic GMP-activated channel activity in excised patches of rod outer segment membrane. Nature. 321:66-70.
20. Hodgkin, A.L., P.A. McNaughton, B.J. Nunn, and K.-W. Yau, 1984. Effects of ions on retinal rods from Bufo marinus. J. Physiol. (Camb.). 350:649-680.
21. Hodgkin, A.L., P.A. McNaughton, and B.J. Nunn. 1985. The ion selectivity and calcium dependence of the light-sensitive pathway in toad rods. J. Physiol. (Camb.). 358:447-468.
22. Horie, M., H. Irisawa, and A. Noma. 1987. Voltage-dependent magnesium block of adenosine-triphosphate-sensitive potassium channel in guinea-pig ventricular cells. J. Physiol. (Camb.). 387: 251-272.
23. Igarashi, K., and K. Williams. 1995. Antagonist properties of polyamines and bis(ethyl)polyamines at N-methyl-D-aspartate receptors. J. Pharmacol. Exp. Ther. 272:1101-1109.
24. 2+ permeable AMPA receptor channels. Neuroreport. 6:2045-2048.
25. Kamboj, S.K., G.T. Swanson, and S.G. Cull-Candy. 1995. Intracellular spermine confers rectification on rat calcium permeable AMPA and kainate receptors. J. Physiol (Camb.). 486:297-303.
26. 2+ in vertebrate photoreceptor excitation and adaptation. Annu. Rev. Physiol. 54:153-175.
27. Kaupp, U.B., T. Niidome, T. Tanabe, S. Terada, W. Baningk, W. Stühmer, N. Cook, K. Kangawa, H. Matsuo, T. Hirose, and S. Numa. 1989. Primary structure and functional expression from complementary DNA of rod photoreceptor cyclic GMP-gated channel. Nature. 342:283-292.
28. 2+-permeable AMPA receptors in rat brain by intracellular polyamines generates double rectification. J. Physiol. (Camb.). 486:305-312.
29. Koutalous, Y., and K.-W. Yau. 1993. A rich complexity emerges in phototransduction. Curr. Opin. Neurobiol. 3:513-519.
30. + channel determined by construction of multimeric cDNAs. Neuron. 9:861-871.
31. Lopatin, A.N., E.N. Makhaaina, and C.G. Nichols. 1994. Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification. Nature. 372:366-369.
32. 2+. Nature. 325:156-159.
33. 2+ of NMDA responses in spinal cord neurons. Nature. 309:261-263.
34. + channel. J. Gen. Physiol. 79:869-891.
35. Nakatani, K., and K.-W. Yau. 1988. Calcium and magnesium fluxes across the plasma membrane of the toad rod outer segment. J. Physiol. (Camb.). 395:695-729.
36. Nowak, L., P. Bregestovski, P. Ascher, A. Herbet, and A. Prochiantz. 1984. Magnesium gates glutamate-activated channels in mouse central neurons. Nature. 307:462-465.
37. Park, C.-S., and R. MacKinnon. 1995. Divalent cation selectivity in a cyclic nucleotide-gated ion channel. Biochemistry. 34:13326-13333.
38. Rock, D.M., and R.L. Macdonald. 1992a. The polyamine spermine has multiple actions on N-methyl-D-aspartate receptor single-channel currents in cultured cortical neurons. Mol. Pharmacol. 41:83-88.
39. Rock, D.M., and R.L. Macdonald. 1992b. Spermine and related polyamines produce a voltage-dependent reduction of N-methyl-D-aspartate receptor single-channel conductance. Mol. Pharmacol. 42:157-164.
40. Root, M.J., and R. MacKinnon. 1993. Identification of an external divalent cation-binding site in the pore of a cGMP-activated channel. Neuron. 11:459-466.
41. Stern, J.H., H. Knutsson, and P.R. Macleish. 1987. Divalent cations directly affect the conductance of excised patches of rod photoreceptor membrane. Science. 236:1674-1678.
42. Torre, V., H.R. Matthews, and T.D. Lamb. 1987. Ion selectivity, blockage and control of light-sensitive conductance. Neurosci. Res. 6:S25-S44.
43. Vandenberg, C.A. 1987. Inward rectification of a potassium channel in cardiac ventricular cells depends on internal magnesium ions. Proc. Natl. Acad. Sci. USA. 84:2560-2564.
44. Werblin, F.S. 1975. Regeneration of hyperpolarization in rods. J. Physiol. (Camb.). 244:53-81.
45. Williams, K. 1997. Modulation and block of ion channels: a new biology of polyamines. Cell Signal 9:1-13.
46. Woodruff, M.L., G.L. Fain, and B.L. Bastian. 1982. Light-dependent ion flux into toad photoreceptors. J. Gen. Physiol. 80:517-536.
47. Yau, K.-W., and D.A. Baylor. 1989. Cyclic CMP-activated conductance of retinal photoreceptor. Annu. Rev. Neurosci. 12:289-327.
48. Yau, K.-W., P.A. McNaughton, and A.L. Hodgkin. 1981. Effects of ions on the light-sensitive current in retinal rods. Nature. 292: 502-505.
49. Yau, K.-W., and K. Nakatini. 1984. Cation selectivity of light-sensitive conductance in retinal rods. Nature. 309:352-354.
50. Zimmerman, A.L., and D.A. Baylor. 1992. Cation interactions within the cyclic GMP-activated channel of retinal rods from the tiger salamander. J. Physiol. (Camb.). 449:759-783.