Development of On and Off retinal pathways and retinogeniculate projections

Progress in Retinal and Eye Research

Volumn 23, Issue 1, 2004, Pages 31-51

  Chalupa, Leo M ^a   Günhan, Emine ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 4 PHOSPHONOBUTYRIC ACID; GLUTAMIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

CELL MATURATION; CHOLINERGIC SYSTEM; CORRELATION ANALYSIS; DENDRITE; ELECTROPHYSIOLOGY; EXTRACELLULAR MATRIX; GENICULATE BODY; GENICULATE NUCLEUS; HUMAN; HYPERPOLARIZATION; INTERNEURON; LIGHT; NERVE CELL NECROSIS; NERVE CELL PLASTICITY; NERVE FIBER; NERVE PROJECTION; NONHUMAN; PRIORITY JOURNAL; RECEPTOR BINDING; REGULATORY MECHANISM; RETINA; RETINA AMACRINE CELL; RETINA BIPOLAR GANGLION CELL; RETINA CONE; RETINA GANGLION CELL; RETINA ROD; REVIEW; STRATIFICATION; VISUAL SYSTEM;

EID: 0842303360     PISSN: 13509462     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.preteyeres.2003.10.001     Document Type: Review

References (84)

1. Akerman C.J., Smyth D., Thompson I.D. Visual experience before eye-opening and the development of the retinogeniculate pathway. Neuron. 36:2002;869-879.
2. Ammermuller J., Kolb H. The organization of the turtle inner retina. I. ON- and OFF-center pathways. J. Comp. Neurol. 358:1995;1-34.
3. Bansal A., Singer J.H., Hwang B.J., Xu W., Beaudet A., Feller M.B. Mice lacking specific nicotinic acetylcholine receptor subunits exhibit dramatically altered spontaneous activity patterns and reveal a limited role for retinal waves in forming ON and OFF circuits in the inner retina. J. Neurosci. 20:2000;7672-7681.
4. Bisti S., Gargini C., Chalupa L.M. Blockade of glutamate-mediated activity in the developing retina perturbs functional segregation of ON and OFF pathways. J. Neurosci. 18:1998;5019-5025.
5. Bodnarenko S.R., Chalupa L.M. Stratification of On and Off ganglion cell dendrites is dependent on glutamate-mediated afferent activity in the developing retina. Nature. 364:1993;144-146.
6. Bodnarenko S.R., Jeyarasasingam G., Chalupa L.M. Development and regulation of dendritic stratification in retinal ganglion cells by glutamate-mediated afferent activity. J. Neurosci. 15:1995;7037-7045.
7. Chalupa L.M., Rhoades R.W. Modification of visual response properties in the superior colliculus of the golden hamster following stroboscopic rearing. J. Physiol. (London). 274:1978;571-592.
8. Chalupa L.M., Rhoades R.W. Directional selectivity in hamster superior colliculus is modified by strobe-rearing but not by dark-rearing. Science. 199:1978;998-1001.
9. Chalupa L.M. Visual physiology of the mammalian superior colliculus. Vanegas H. Comparative Neurology of the Optic Tectum. 1984;775-818 Plenum Press, New York.
10. Chalupa L.M., Williams R.W., Henderson Z. Binocular interaction in the fetal cat regulates the size of the ganglion cell population. Neuroscience. 12:1984;1139-1146.
11. Chalupa L.M., Jeyarasasingam G., Snider C., Bodnarenko S.R. Development of ON and OFF ganglion cell mosaics in cat retina. Chalupa L.M., Finlay B.L. Development and Organization of the Retina: From Molecules to Function. 1998;77-89 Plenum Press, New York.
12. Chun M.H., Kim I.B., Oh S.J., Chung J.W. Synaptic connectivity of two types of recoverin-labeled cone bipolar cells and glutamic acid decarboxylase immunoreactive amacrine cells in the inner plexiform layer of the rat retina. Vis. Neurosci. 16:1999;791-800.
13. Cook J. Spatial regularity among retinal neurons. Chalupa L.M., Werner J.S. The Visual Neurosciences. 2003;463-477 MIT Press, Cambridge, MA.
14. Cook J., Chalupa L.M. Retinal mosaics. New insights on an old concept Trends Neurosci. 23:2000;26-34.
15. Cramer K.S., Sur M. Blockade of afferent impulse activity disrupts ON/ OFF sublamination in the ferret lateral geniculate nucleus. Dev. Brain Res. 98:1997;287-290.
16. Dann J.F., Buhl E.H., Peichl L. Postnatal dendritic maturation of alpha and beta ganglion cells in cat retina. J. Neurosci. 8:1988;1485-1499.
17. DeVries S.H. Bipolar cells use kainate and AMPA receptors to filter visual information into separate channels. Neuron. 28:2000;847-856.
18. Dizhoor A.M., Ray S., Kumar S., Niemi G., Spencer M., Brolley D., Walsh K.A., Philipov P.P., Hurley J.B., Stryer L. Recoverin. a calcium sensitive activator of retinal rod guanylate cyclase Science. 251:1991;915-918.
19. Dubin M.W., Stark L.A., Archer S.M. A role for action-potential activity in the development of neuronal connections in the kitten retinogeniculate pathway. J. Neurosci. 6:1986;1021-1036.
20. Euler T., Wässle H. Immunocytochemical identification of cone bipolar cells in the rat retina. J. Comp. Neurol. 361:1995;461-478.
21. Famiglietti E.V. Dendritic co-stratification of ON and On-Off directionally selective ganglion cells with starburst amacrine cells in rabbit retina. J. Comp. Neurol. 324:1992;322-335.
22. Famiglietti E.V. Jr., Kolb H. Structural basis for ON-and OFF center responses in retinal ganglion cells. Science. 194:1976;193-195.
23. Galli-Resta L., Resta G., Tan S.S., Reese B.E. Mosaics of islet-1-expressing amacrine cells assembled by short-range cellular interactions. J. Neurosci. 17:1997;7831-7838.
24. Galli-Resta L., Novelli E., Volpini M., Strettoi E. The spatial organization of cholinergic mosaics in the adult mouse retina. Eur. J. Neurosci. 12(10):2000;3819-3822.
25. Günhan-Agar E., Kahn D., Chalupa L.M. Segregation of On and Off bipolar cell axonal arbors in the absence of retinal ganglion cells. J. Neurosci. 20:2000;308-314.
26. Günhan E., Choudary P.V., Landerholm T.E., Chalupa L.M. Depletion of cholinergic amacrine cells by a novel immunotoxin does not perturb the formation of segregated On and Off cone bipolar cell projections. J. Neurosci. 22:2002;265-2273.
27. Günhan E., Van der List D., Chalupa L.M. Ectopic photoreceptors and cone bipolar cells in the developing and mature retina. J. Neurosci. 23:2003;1383-1389.
28. Hack I., Peichl L., Brandstatter J.H. An alternative pathway for rod signals in the rodent retina. rod photoreceptors, cone bipolar cells, and the localization of glutamate receptors Proc. Natl. Acad. Sci. USA. 96:1999;14130-14135.
29. Hahm J.O., Langdon R.B., Sur M. Disruption of retinogeniculate afferent segregation by antagonists to NMDA receptors. Nature. 351:1991;568-570.
30. Hahm J.O., Cramer K.S., Sur M. Pattern formation by retinal afferents in the ferret lateral geniculate nucleus. developmental segregation and the role of N-methyl-D-aspartate receptors J. Comp. Neurol. 411:1999;327-345.
31. Hartline H.K. The response of single optic nerve fibers of the vertebrate eye to illumination of the retina. Am. J. Physiol. 121:1938;400-415.
32. Hebb D.O. The Organization of Behavior. 1949;Wiley, New York.
33. Huberman A.D., Gunhan-Agar E., Choudary P.V., Landerholm T.E., Chalupa L.M. Combined elimination of ganglion and cholinergic amacrine cells severely perturbs retinal development. Soc. Neurosci. Abs. 31:2001;659.
34. Huberman A., Wang G.-Y., Liets L.C., Collins O.A., Chapman B., Chalupa L.M. Eye-specific retinogeniculate segregation independent of normal neuronal activity. Science. 300:2003;994-998.
35. Jeyarasasingam G., Snider C.J., Ratto G.M., Chalupa L.M. Activity-regulated cell death contributes to the formation of ON and OFF alpha ganglion cell mosaics. J. Comp. Neurol. 394:1998;335-343.
36. Kuffler S.W. Discharge patterns and functional organization of mammalian retina. J. Neurophysiol. 16:1953;47-68.
37. Lambrecht H.G., Koch K.W. Recoverin, a novel calcium-binding protein from vertebrate photoreceptors. Biochim. Biophys. Acta. 1160:1992;63-66.
38. Lee C.W., Eglen S.J., Wong R.O. Segregation of ON and OFF retinogeniculate connectivity directed by patterned spontaneous activity. J. Neurophysiol. 88:2002;2311-2321.
39. LeVay S., McConnell S.K. ON and OFF layers in the lateral geniculate nucleus of the mink. Nature. 300:1982;350-351.
40. Liets L.C., Chalupa L.M. The metabotropic glutamate agonist 2-amino-4-phosphonobutryric acid (APB) does not activate currents in postnatal retinal ganglion cells. NeuroReport. 7:1996;2873-2877.
41. Liets L.C., Olshausen B.A., Wang G.-Y., Chalupa L.M. Spontaneous activity of morphologically identified ganglion cells in the developing ferret retina. J. Neurosci. 23:2003;7343-7350.
42. Linden D.C., Guillery R.W., Cucchiaro J. The dorsal lateral geniculate nucleus of the normal ferret and its postnatal development. J. Comp. Neurol. 203:1981;89-211.
43. Maslim J., Stone J. Synaptogenesis in the retina of the cat. Brain Res. 373:1986;35-48.
44. Maslim J., Stone J. Time course of stratification of the dendritic fields of ganglion cells in the retina of the cat. Brain Res. Dev. Brain Res. 44:1988;87-93.
45. McGinnis J.F., Stepanik P.L., Chen W., Elias R., Cao W., Lerious V. Unique retina cell phenotypes revealed by immunological analysis of recoverin expression in rat retina cells. J. Neurosci. Res. 55:1999;252-260.
46. Milam A.H., Dacey D.M., Dizhoor A.M. Recoverin immunoreactivity in mammalian cone bipolar cells. Vis. Neurosci. 10:1993;1-12.
47. Miller E.D., Tran M.N., Wong G.K., Oakley D.M., Wong R.O.L. Morphological differentiation of bipolar cells in the ferret retina. Vis. Neurosci. 16:1999;1133-1144.
48. Nakajima Y., Iwakabe H., Akazawa C., Nawa H., Shigemoto R., Mizuno N., Nakanishi S. Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4- phosphonobutyrate. J. Biol. Chem. 268:1993;11868-11873.
49. Nelson R., Kolb H. ON and OFF pathways in the vertebrate retina and visual system. Chalupa L.M., Werner J.S. The Visual Neurosciences. 2003;260-278 MIT Press, Cambridge, MA.
50. Nelson R., Famiglietti E.V.J., Kolb H. Intracellular staining reveals different levels of stratification for on- and off-center ganglion cells in the cat retina. J. Neurophysiol. 41:1978;472-483.
51. Nomura A., Shigemoto R., Nakamura Y., Okamoto N., Mizuno N., Nakanishi S. Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells. Cell. 77:1994;361-369.
52. Okada M., Erickson A., Hendrickson A. Light and electron microscopic analysis of synaptic development in Macaca monkey retina as detected by immunocytochemical labeling for the synaptic vesicle protein, SV2. J. Comp. Neurol. 339:1994;535-558.
53. Olson C.R., Freeman R.D. Monocular deprivation and recovery during sensitive period in kittens. J. Neurophysiol. 41:1978;6574.
54. Rakic P. Cell migration and neuronal ectopias in the brain. Birth Defects Orig. Artic. Ser. 11:1975;95-129.
55. Rakic P. Mechanism of ocular dominance segregation in the lateral geniculate nucleus. competitive elimination hypothesis Trends Neurosci. 9:1986;11-15.
56. Rakic P. Defects of neuronal migration and the pathogenesis of cortical malformations. Prog. Brain Res. 73:1988;15-37.
57. Rakic P., Riley K.P. Regulation of Axon number in primate optic nerve by prenatal binocular competition. Nature. 305:1983;135-137.
58. Reese B.E., Necessary B.D., Tam P.P., Faulkner-Jones B., Tan S.S. Clonal expansion and cell dispersion in the developing mouse retina. Eur. J. Neurosci. 11:1999;2965-2978.
59. Scheetz A.J., Williams R.W., Dubin M.W. Severity of ganglion cell death during early postnatal development is modulated by both neuronal activity and binocular competition. Vis. Neurosci. 12:1995;605-610.
60. Sharpe L.T., Stockman A. Rod pathways. the importance of seeing nothing Trends Neurosci. 22:1999;497-504.
61. Sherman S.M., Guillery R.W. The visual relays in the thalamus. Chalupa L.M., &Werner J.S. The Visual Neurosciences. 2003;565-591 MIT Press, Cambridge, MA.
62. Slaughter M.M., Miller R.F. 2-Amino-4-phosphonobutyric acid. a new pharmacological tool for retina research Science. 211:1981;182-185.
63. Soucy E., Wang Y., Nirenberg S., Nathans J., Meister M. A novel signaling pathway from rod photoreceptors to ganglion cells in mammalian retina. Neuron. 21:1998;481-493.
64. Stein B.E., Labos E., Kruger L. Sequence of changes in properties of neurons of superior colliculus of the kitten during maturation. J. Neurophysiol. 36:1973;667-679.
65. Stepanik P.L., Lerious V., McGinnis J.F. Developmental appearance, species and tissue specificity of mouse 23-kDa, a retinal calcium-binding protein (recoverin). Exp. Eye Res. 57:1993;189-197.
66. Sterling P. Retina. Shepherd G.M. The Synaptic Organization of the Brain. 1998;205-253 Oxford University Press, New York.
67. Sterling P. How retinal circuits optimize the transfer of visual information. Chalupa L.M., Werner J.S. The Visual Neurosciences. 2003;234-259 MIT Press, Cambridge, MA.
68. Stryker M.P., Zahs K.R. On and off sublaminae in the lateral geniculate nucleus of the ferret. J. Neurosci. 3:1983;1943-1951.
69. Tagawa Y., Sawai H., Ueda Y., Tauchi M., Nakanishi S. Immunohistological studies of metabotropic glutamate receptor subtype 6-deficient mice show no abnormality of retinal cell organization and ganglion cell maturation. J. Neurosci. 19:1999;2568-2579.
70. Tian N., Copenhagen D.R. Visual stimulation is required for refinement of ON and OFF pathways in postnatal retina. Neuron. 39:2003;85-96.
71. Tootle J.S. Early postnatal development of visual function in ganglion cells of the cat retina. J. Neurophysiol. 69:1993;1645-1660.
72. Wang G.-Y., Liets L.C., Chalupa L.M. Unique functional properties of On and Off pathways in the developing mammalian retina. J. Neurosci. 21:2001;4310-4317.
73. Wassle H., Riemann H.J. The mosaic of nerve cells in the mammalian retina. Proc. R. Soc. Lond. B Biol. Sci. 200(1141):1978;441-461.
74. Werblin F.S., Dowling J.E. Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. J. Neurophysiol. 32:1969;339-355.
75. Wiechmann A.F., Hammarback J.A. Expression of recoverin mRNA in the human retina. localization by in situ hybridization Exp. Eye Res. 57:1993;763-769.
76. Williams R.W., Chalupa L.M. An analysis of axon caliber within the optic nerve of the cat. evidence of size groupings and regional organization J. Neurosci. 3:1983;1554-1564.
77. Williams R.W., Bastiani M.J., Chalupa L.M. Loss of axons following fetal unilateral enucleation. an electron microscopic analysis J. Neurosci. 3:1983;133-144.
78. Williams R.W., Bastiani M.J., Lia B., Chalupa L.M. Growth cones, dying axons, and developmental fluctuations in the fiber population of the cat's optic nerve. J. Comp. Neurol. 246:1986;32-69.
79. Wong R.O.L. Retinal waves and visual system development. Annu. Rev. Neurosci. 22:1999;29-47.
80. Wong R.O.L., Oakley D.M. Changing patterns of spontaneous bursting activity of on and off retinal ganglion cells during development. Neuron. 16:1996;1087-1095.
81. Wong R.O.L., Godinho L. Development of the vertebrate retina. Chalupa L.M., Werner J.S. The Visual Neurosciences. 2003;77-93 MIT Press, Cambridge, MA.
82. Yan X.X., Wiechmann A.F. Early expression of recoverin in a unique population of neurons in the human retina. Anat. Embryol. (Berl). 195:1997;51-63.
83. Zhan X.J., Troy J.B. Modeling cat retinal beta-cell arrays. Vis. Neurosci. 17:2000;23-39.
84. Zhou Z.J. The function of the cholinergic system in the developing mammalian retina. Prog. Brain Res. 131:2001;599-614.