Expression of the neurokinin 1 receptor in the rabbit retina

Neuroscience

Volumn 115, Issue 4, 2002, Pages 1309-1321

  Casini, G ^a   Sabatini, A ^a   Catalani, E ^a   Willems, D ^a   Bosco, L ^a   Brecha, N C ^b,c  

^a UNIVERSITY OF TUSCIA   (Italy)

^b JULES STEIN EYE INSTITUTE   (United States)

^c VA GREATER LOS ANGELES HEALTHCARE SYSTEM   (United States)

Author keywords

Amacrine cells; Bipolar cells; Dopamine; Neuropeptide receptors; Photoreceptors; Substance P

Indexed keywords

NEUROKININ 1 RECEPTOR; RECEPTOR ANTIBODY; TYROSINE 3 MONOOXYGENASE;

ANIMAL TISSUE; ARTICLE; BRAIN REGION; CELL DENSITY; CELL POPULATION; CONTROLLED STUDY; IMMUNOCYTOCHEMISTRY; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; NERVE CELL; NERVE FIBER; NONHUMAN; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN PURIFICATION; RABBIT; RETINA; RETINA AMACRINE CELL; RETINA BIPOLAR GANGLION CELL; RETINA NERVE CELL;

AMACRINE CELLS; ANIMALS; AXONS; DENDRITES; DOPAMINE; IMMUNOHISTOCHEMISTRY; NEURAL PATHWAYS; NEURONS; RABBITS; RECEPTORS, NEUROKININ-1; RETINA; RETINAL GANGLION CELLS; SUBSTANCE P; SYNAPSES; SYNAPTIC TRANSMISSION; TYROSINE 3-MONOOXYGENASE; VISION;

EID: 0037121664     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(02)00408-6     Document Type: Article

References (74)

1. Ayoub G.S., Matthews G. Substance P modulates calcium current in retinal bipolar neurons. Vis. Neurosci. 8:1992;539-544.
2. Bartho L., Holzer P. Search for a physiological role of substance P in gastrointestinal motility. Neuroscience. 16:1985;1-32.
3. Bloomfield S.A., Dacheux R.F. Rod vision: pathways and processing in the mammalian retina. Prog. Retinal Eye Res. 20:2001;351-384.
4. Boelen M.K., Boelen M.G., Marshak D.W. Light-stimulated release of dopamine from the primate retina is blocked by 1-2-amino-4-phosphonobutyric acid (APB). Vis. Neurosci. 15:1998;97-103.
5. Brecha N.C., Johnson D., Bolz J., Sharma S., Parnavelas J.G., Lieberman A.R. Substance P-immunoreactive retinal ganglion cells and their central axon terminals in rabbit. Nature. 327:1987;155-158.
6. Brown S.P., Masland R.H. Costratification of a population of bipolar cells with the direction-selective circuitry of the rabbit retina. J. Comp. Neurol. 408:1999;97-106.
7. Cajal S.R. La rétine des vertébrés. Cellule. 9:1893;119-257.
8. Caruso D.M., Owczarzak M.T., Pourcho R.G. Colocalization of substance P and GABA in retinal ganglion cells: a computer-assisted visualization. Vis. Neurosci. 5:1990;389-394.
9. Casini G., Brecha N.C. Postnatal development of tyrosine hydroxylase immunoreactive amacrine cells in the rabbit retina. I. Morphological characterization. J. Comp. Neurol. 326:1992;283-301.
10. Casini G., Brecha N.C. Postnatal development of tyrosine hydroxylase immunoreactive amacrine cells in the rabbit retina. II. Quantitative analysis. J. Comp. Neurol. 326:1992;302-313.
11. Casini G., Brecha N.C., Bosco L., Rickman D.W. Developmental expression of neurokinin-1 and neurokinin-3 receptors in the rat retina. J. Comp. Neurol. 421:2000;275-287.
12. Casini G., Grassi A., Trasarti L., Bagnoli P. Developmental expression of protein kinase C immunoreactivity in rod bipolar cells of the rabbit retina. Vis. Neurosci. 13:1996;817-831.
13. Casini G., Rickman D.W., Brecha N.C. The AII amacrine cell population in the rabbit retina: identification with parvalbumin immunoreactivity. J. Comp. Neurol. 355:1995;1-11.
14. Casini G., Rickman D.W., Sternini C., Brecha N.C. Neurokinin 1 receptor expression in the rat retina. J. Comp. Neurol. 389:1997;496-507.
15. Casini G., Sabatini A., Trasarti L., Catalani E., Marroni P., Bosco L., Brecha N.C. Neurokinin 1 (NK1) receptor expression in rabbit retina. Soc. Neurosci. Abstr. 26:2000;2152.
16. Casini G., Trasarti L., Andolfi L., Bagnoli P. Morphologic maturation of tachykinin peptide-expressing cells in the postnatal rabbit retina. Dev. Brain Res. 99:1997;131-141.
17. Chen L.W., Wei L.C., Liu H.L., Duan L., Ju G., Chan Y.S. Retinal dopaminergic neurons (A17) expressing neuromedin K receptor (NK(3)): a double immunocytochemical study in the rat. Brain Res. 885:2000;122-127.
18. 1) in the rabbit retina. Invest. Ophthalmol. Vis. Sci. 41:2000;3191-3199.
19. Cuenca N., Kolb H. Circuitry and role of substance P-immunoreactive neurons in the primate retina. J. Comp. Neurol. 393:1998;439-456.
20. Dick E., Miller R.F. Peptides influence retinal ganglion cells. Neurosci. Lett. 26:1981;131-135.
21. Djamgoz M.B., Wagner H.J. Localization and function of dopamine in the adult vertebrate retina. Neurochem. Int. 20:1992;139-191.
22. Eberhardt L.L. Some developments in 'distance sampling'. Biometrics. 23:1967;207-216.
23. Euler T., Wässle H. Immunocytochemical identification of cone bipolar cells in the rat retina. J. Comp. Neurol. 361:1995;461-478.
24. Famiglietti E.V. Functional architecture of cone bipolar cells in mammalian retina. Vis. Res. 21:1981;1559-1563.
25. Famiglietti E.V., Kolb H. Structural basis for ON- and OFF-center responses in retinal ganglion cells. Science. 194:1976;193-195.
26. Famiglietti E.V., Sharpe S.J. Regional topography of rod and immunocytochemically characterized 'blue' and 'green' cone photoreceptors in rabbit retina. Vis. Neurosci. 12:1995;1151-1175.
27. Fontanesi G., Gargini C., Bagnoli P. Postnatal development of somatostatin 2A (sst2A) receptors expression in the rabbit retina. Dev. Brain Res. 123:2000;67-80.
28. Glickman R.D., Adolph A.R., Dowling J.E. Inner plexiform circuits in the carp retina: effects of cholinergic agonists, GABA, and substance P on the ganglion cells. Brain Res. 234:1982;81-99.
29. Goehler L.E., Sternini C., Brecha N.C. Calcitonin gene-related peptide immunoreactivity in the biliary pathway and liver of the guinea pig: distribution and colocalization with substance P. Cell Tissue Res. 253:1988;145-150.
30. Greferath U., Grünert U., Wässle H. Rod bipolar cells in the mammalian retina show protein kinase C-like immunoreactivity. J. Comp. Neurol. 301:1990;433-442.
31. Hampson E.C.G.M., Vaney D.I., Weiler R. Dopaminergic modulation of gap junction permeability between amacrine cells in mammalian retina. J. Neurosci. 12:1992;4911-4922.
32. Hartveit E. Functional organization of cone bipolar cells in the rat retina. J. Neurophysiol. 4:1997;1716-1730.
33. 2 in the rat retina. Invest. Ophthalmol. Vis. Sci. 40:1999;2376-2382.
34. Ishimoto I., Millar T., Chubb I.W., Morgan I.G. Somatostatin-immunoreactive amacrine cells of chicken retina: retinal mosaic, ultrastructural features, and light-driven variations in peptide metabolism. Neuroscience. 17:1986;1217-1233.
35. Jensen R.J. Mechanism and site of action of a dopamine D1 antagonist in the rabbit retina. Vis. Neurosci. 3:1989;573-585.
36. Jeon C.J., Masland R.H. A population of wide-field bipolar cells in the rabbit's retina. J. Comp. Neurol. 360:1995;403-412.
37. Johnson J., Wong H., Walsh J.H., Brecha N.C. Expression of the somatostatin subtype 2A receptor in the rabbit retina. J. Comp. Neurol. 393:1998;93-101.
38. Johnson J., Wu V., Wong H., Walsh J.H., Brecha N.C. Somatostatin receptor subtype 2A expression in the rat retina. Neuroscience. 94:1999;675-683.
39. Jonsson G., Hallman H. Substance P counteracts neurotoxin damage on norepinephrine neurons in rat brain during ontogeny. Science. 125:1982;75-77.
40. Jonsson G., Hallman H. Substance P modifies the 6-hydroxydopamine induced alteration of postnatal development of central noradrenaline neurons. Neuroscience. 7:1982;2909-2918.
41. Kolb H., Cuenca N., Dekorver L. Postembedding immunocytochemistry for GABA and glycine reveals the synaptic relationships of the dopaminergic amacrine cell of the cat retina. J. Comp. Neurol. 310:1991;267-284.
42. Kolb H., Cuenca N., Wang H.H., Dekorver L. The synaptic organization of the dopaminergic amacrine cell in the cat retina. J. Neurocytol. 19:1990;343-366.
43. Kolb H., Fernandez E., Ammermuller J., Cuenca N. Substance P: a neurotransmitter of amacrine and ganglion cells in the vertebrate retina. Histol. Histopathol. 10:1995;947-968.
44. Kondoh A., Houtani T., Ueyama T., Baba K., Ikeda M., Yamagishi K., Miki H., Uyama M., Nakanishi S., Sugimoto T. In situ hybridization analysis of substance P receptor in the rat retina. Exp. Brain Res. 112:1996;181-186.
45. Lambrecht H.-G., Koch K.-W. Recoverin, a novel calcium binding protein from vertebrate photoreceptors. Biochim. Biophys. Acta. 1160:1992;63-66.
46. Li H.B., So K.F., Cheuk W. Substance P-immunoreactive neurons in hamster retinas. Vis. Neurosci. 16:1999;475-481.
47. Maggio J.E. Tachykinins. Annu. Rev. Neurosci. 11:1988;13-28.
48. Massey S.C., Mills S.L. A calbindin-immunoreactive cone bipolar cell type in the rabbit retina. J. Comp. Neurol. 366:1996;15-33.
49. McGillem G.S., Dacheux R.F. Rabbit cone bipolar cells: correlation of their morphologies with whole-cell recordings. Vis. Neurosci. 18:2001;675-685.
50. Merighi A., Raviola E., Dacheux R.F. Connections of two types of flat cone bipolars in the rabbit retina. J. Comp. Neurol. 371:1996;164-178.
51. Mills S.L., Massey S.C. Morphology of bipolar cells labeled by DAPI in the rabbit retina. J. Comp. Neurol. 321:1992;133-149.
52. Nelson R., Famiglietti E.V., Kolb H. Intracellular staining reveals different levels of stratification for on-center and off-center ganglion cells in the cat retina. J. Neurophysiol. 4:1978;427-483.
53. Nelson R., Kolb H. Synaptic patterns and response properties of bipolar and ganglion cells in the cat retina. Vis. Res. 23:1983;1183-1195.
54. Nilsson J., von Euler A.M., Dalsgaard C.J. Stimulation of connective tissue cell growth by substance P and substance K. Nature. 315:1985;61-63.
55. Onoda N., Fujita S.C. A monoclonal antibody specific for a subpopulation of retinal bipolar cells in the frog and other vertebrates. Brain Res. 416:1987;359-363.
56. Otsuka M., Yoshioka K. Neurotransmitter functions of mammalian tachykinins. Physiol. Rev. 73:1993;229-308.
57. Oyamada H., Takatsuji K., Senba E., Manthy P.W., Tohyama M. Postnatal development of NK1, NK2 and NK3 neurokinin receptors expression in the rat retina. Dev. Brain Res. 117:1999;59-70.
58. Peichl L., Wässle H. Morphological identification of ON- and OFF-centre brisk transient (Y) cells in the cat retina. Proc. R. Soc. London B Biol. Sci. 212:1981;139-153.
59. Pernow B. Substance P. Pharmacol. Rev. 35:1983;85-141.
60. Pourcho R.G. Dopaminergic amacrine cells in the cat retina. Brain Res. 252:1982;101-109.
61. Rickman D.W., Blanks J.C., Brecha N.C. Somatostatin-immunoreactive neurons in the adult rabbit retina. J. Comp. Neurol. 365:1996;491-503.
62. Rohrer H., Acheson A.L., Thibault J., Thoenen H. Developmental potential of quail dorsal root ganglion cells analyzed in vitro and in vivo. J. Neurosci. 6:1986;2616-2624.
63. Shughrue P.J., Lane M.V., Merchenthaler I. In situ hybridization analysis of the distribution of neurokinin-3 mRNA in the rat central nervous system. J. Comp. Neurol. 372:1996;395-414.
64. Takatsuji K., Miguel-Hidalgo J.J., Tohyama M. Substance P-immunoreactive innervation from the retina to the suprachiasmatic nucleus in the rat. Brain Res. 568:1991;223-229.
65. Tsang, D., 1986. Effect of substance P on dopamine release in rat retina. In: Kon, O.L., Chung, M.C.M., Hwang, P.L.H., Leong, S.F., Loke, K.H., Thiayagarajah, P., Wong, P.H.T. (Eds.), Contemporary Themes in Biochemistry. Cambridge University Press, Cambridge, pp. 588-589.
66. Versaux-Botteri C., Martin-Martinelli E., Nguyen-Legros J., Geffard M., Vigny A., Denoroy L. Regional specialization of the rat retina: catecholamine-containing amacrine cell characterization and distribution. J. Comp. Neurol. 243:1986;422-433.
67. Vigna S.R., Bowden J.J., McDonald D.M., Fisher J., Okamoto A., McVey D.C., Payan D.J., Bunnett N.W. Characterization of antibodies to the rat substance P (NK-1) receptor and to a chimeric substance P receptor expressed in mammalian cells. J. Neurosci. 14:1994;834-845.
68. Voigt T., Wässle H. Dopaminergic innervation of AII amacrine cells in mammalian retina. J. Neurosci. 7:1987;4115-4128.
69. Wässle H., Boycott B.B. Functional architecture of the mammalian retina. Physiol. Rev. 71:1991;447-480.
70. Wässle H., Riemann H.J. The mosaic of nerve cells in the mammalian retina. Proc. R. Soc. London B Biol. Sci. 200:1978;441-461.
71. Yang D.S., Li Z.K., Morgan I.G. A light-driven rhythm in neurotensin-like immunoreactivity in the chicken retina. Aust. New Zealand J. Ophthalmol. 1:(Suppl):1997;S67-D69.
72. Young H.M., Vaney D.I. Rod-signal interneurons in the rabbit retina. 1. Rod bipolar cells. J. Comp. Neurol. 310:1991;139-153.
73. Zalutsky R.A., Miller R.F. The physiology of substance P in the rabbit retina. J. Neurosci. 10:1990;394-402.
74. Zalutsky R.A., Miller R.F. The physiology of somatostatin in the rabbit retina. J. Neurosci. 10:1990;383-393.