Postnatal development of parvalbumin immunoreactive amacrine cells in the rabbit retina

Developmental Brain Research

Volumn 111, Issue 1, 1998, Pages 107-117

  Casini, Giovanni ^a   Rickman, Dennis W ^b   Trasarti, Luigi ^a   Brecha, Nicholas C ^c,d  

^a UNIVERSITY OF TUSCIA   (Italy)

^b UNIVERSITY OF IOWA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

All amacrine cell; Calcium binding protein; Retina development; Rod pathway

Indexed keywords

PARVALBUMIN;

ANIMAL CELL; ARTICLE; IMMUNOHISTOCHEMISTRY; NEWBORN; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RABBIT; RETINA AMACRINE CELL; RETINA DEVELOPMENT;

AGING; ANIMALS; ANIMALS, NEWBORN; CELL COUNT; IMMUNOHISTOCHEMISTRY; PARVALBUMINS; RABBITS; RETINA;

EID: 0032212046     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-3806(98)00127-8     Document Type: Article

References (65)

1. Casini G., Brecha N.C. Vasoactive intestinal polypeptide-containing cells in the rabbit retina: immunohistochemical localization and quantitative analysis. J. Comp. Neurol. 305:1991;313-327.
2. Casini G., Brecha N.C. Postnatal development of tyrosine hydroxylase immunoreactive neurons in the rabbit retina: I. Morphological characterization. J. Comp. Neurol. 326:1991;283-301.
3. Casini G., Brecha N.C. Postnatal development of tyrosine hydroxylase immunoreactive neurons in the rabbit retina: II. Quantitative analysis. J. Comp. Neurol. 326:1992;302-313.
4. Casini G., Rickman D.W., Brecha N.C. Parvalbumin immunoreactivity in the developing rabbit retina. Invest. Ophthalmol. Vis. Sci. 33:1992;694.
5. Casini G., Molnar M., Brecha N.C. Vasoactive intestinal polypeptide/peptide histidine isoleucine mRNA in the rat retina: adult distribution and developmental expression. Neuroscience. 58:1994;657-667.
6. 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.
7. 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.
8. 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.
9. Celio M.R. Calbindin D-28 k and parvalbumin in the rat nervous system. Neuroscience. 35:1990;375-475.
10. Celio M.R., Baier W., de Virag P., Scährer E., Gerday Ch. Monoclonal antibodies directed against the calcium binding protein parvalbumin. Cell Calcium. 9:1988;81-86.
11. Chun M.-H., Han S.-H., Chung J.-W., Wässle H. Electron microscopic analysis of the rod pathway of the rabbit retina. J. Comp. Neurol. 332:1993;421-432.
12. Crooks J., Kolb H. Localization of GABA, glycine, glutamate and tyrosine hydroxylase in the human retina. J. Comp. Neurol. 315:1992;287-302.
13. Dacheux R.F., Miller R.F. An intracellular electrophysiological study of the ontogeny of functional synapses in the rabbit retina: II. Amacrine cells. J. Comp. Neurol. 198:1981;327-334.
14. Dacheux R.F., Raviola E. The rod pathway in the rabbit retina: a depolarizing bipolar and amacrine cell. J. Neurosci. 6:1986;331-345.
15. Dann J.F. Cholinergic amacrine cells in the developing cat retina. J. Comp. Neurol. 289:1981;143-155.
16. Eberhardt L.L. Some developments in 'distance sampling'. Biometrics. 23:1967;207-216.
17. Endo T., Kobayashi S., Onaya T. Parvalbumin in rat cerebrum, cerebellum and retina during postnatal development. Neurosci. Lett. 603:1985;279-282.
18. Endo T., Kobayashi M., Kobayashi S., Onaya T. Immunocytochemical and biochemical localization of parvalbumin in the retina. Cell Tissue Res. 243:1986;213-217.
19. Famiglietti E.V., Kolb H. A bistratified amacrine cell and synaptic circuitry in the inner plexiform layer of the retina. Brain Res. 84:1975;293-300.
20. Frederick J.M., Rayborn M.E., Hollyfield J.G. Glycinergic neurons in the human retina. J. Comp. Neurol. 227:1984;159-172.
21. Fung S.-C., Kong Y.-C., Lam D.M.-K. Prenatal development of GABAergic, glycinergic, and dopaminergic neurons in the rabbit retina. J. Neurosci. 11:1982;1623-1632.
22. Gábriel R., Straznicky C. Immunocytochemical localization of parvalbumin- and neurofilament triplet protein immunoreactivity in the cat retina: colocalization in a subpopulation of AII amacrine cells. Brain Res. 595:1992;133-136.
23. Greiner J.V., Weidman T.A. Embryogensis of the rabbit retina. Exp. Eye Res. 34:1982;749-765.
24. Guo Q.X., Yu M.C., Garey L.J., Jen L.S. Development of parvalbumin immunoreactive neurons in normal and intracranially transplanted retinas in the rat. Exp. Brain Res. 90:1992;359-368.
25. Hamano K., Kiyama H., Emson P.C., Manabe R., Nakauchi M., Tohyama M. Localization of two calcium binding proteins, calbindin (28 kD) and parvalbumin (12 kD), in the vertebrate retina. J. Comp. Neurol. 302:1990;417-424.
26. Hendrickson A.E., Koontz M.A., Pourcho R.G., Sarthy P.V., Goebel D.J. Localization of glycine-containing neurons in the Macaca monkey retina. J. Comp. Neurol. 273:1988;473-487.
27. Holt C.E., Bertsch T.W., Ellis H.M., Harris W.A. Cellular determination in the Xenopus retina is independent of lineage and birth date. Neuron. 1:1988;15-26.
28. 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.
29. 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.
30. Kong Y.-C., Fung S.-C., Lam D.M.-K. The postnatal development of glycinergic neurons in rabbit retina. J. Comp. Neurol. 193:1980;1127-1135.
31. Lam D.M.-K., Fung S.-C., Kong Y.-C. The postnatal development of GABAergic neurons in the rabbit retina. J. Comp. Neurol. 193:1980;89-102.
32. McArdle C.B., Dowling J.E., Masland R.H. Development of outer segments and synapses in the rabbit retina. J. Comp. Neurol. 175:1977;253-273.
33. 3H] Glycine-accumulating neurons of the human retina J. Comp. Neurol. 232:1985;241-260.
34. Masland R.H. Maturation of functions in the developing rabbit retina. J. Comp. Neurol. 175:1977;275-286.
35. Masland R.H., Rizzo J.F., Sandell J.H. Developmental variation in the structure of the retina. J. Neurosci. 13:1993;5194-5202.
36. Mitrofanis J., Robinson S.R., Ashwell K. Development of catecholaminergic, indoleamine-accumulating and NADPH-diaphorase amacrine cells in rabbit retinae. J. Comp. Neurol. 319:1992;560-585.
37. 3H) -GABA by amacrine cells in the cat retina Brain Res. 198:1980;333-346.
38. Pourcho R.G. Dopaminergic amacrine cells in the cat retina. Brain Res. 252:1982;101-109.
39. 3H) -glycine-accumulating amacrine cells in the cat retina J. Comp. Neurol. 233:1985;473-480.
40. Pourcho R.G., Owczarzak M.T. Connectivity of glycine immunoreactive amacrine cells in the cat retina. J. Comp. Neurol. 307:1991;549-561.
41. Pow D.V., Cook D.K., Wong R.O.L. Early appearance and transient expression of putative amino acid neurotransmitters and related molecules in the developing rabbit retina: an immunocytochemical study. Vis. Neurosci. 11:1994;1115-1134.
42. Reh T.A., Radke K. A role for the extracellular matrix molecules in retinal neurogenesis in vitro. Dev. Biol. 129:1988;283-293.
43. Reh T.A., Tully T. Regulation of tyrosine hydroxylase-containing amacrine cell number in larval frog retina. Dev. Biol. 114:1986;463-469.
44. Robinson S.R., Dreher B., McCall M.J. Nonuniform retinal expansion during the formation of the rabbit's visual streak: implications for the ontogeny of mammalian retinal topography. Vis. Neurosci. 2:1989;201-219.
45. Robinson S.R., Dangerfield F.C., Dreher B., Rapaport D.H. Neuronal birth and loss in developing rabbit retinae. Soc. Neurosci. Abstr. 17:1992;1125.
46. Röhrenbeck J., Wässle H., Heizmann H. Immunocytochemical labeling of horizontal cells in mammalian retina using antibodies against calcium binding proteins. Neurosci. Lett. 77:1987;255-260.
47. Röhrenbeck J., Wässle H., Boycott B.B. Horizontal cells in the monkey retina: immunocytochemical staining with antibodies against calcium binding proteins. Eur. J. Neurosci. 1:1989;407-420.
48. Sanna P.P., Keyser K.T., Battenberg E., Bloom F.E. Parvalbumin immunoreactivity in the rat retina. Neurosci. Lett. 118:1990;136-139.
49. Sanna P.P., Keyser K.T., Celio M.R., Karten H.J., Bloom F.E. Distribution of parvalbumin immunoreactivity in the vertebrate retina. Brain Res. 600:1993;141-150.
50. Smith R.G., Freed M.A., Sterling P. Microcircuitry of the dark-adapted cat retina: functional architecture of the rod-cone network. J. Neurosci. 6:1986;3505-3517.
51. Sterling P., Freed M.A., Smith R.G. Architecture of rod and cone circuits to the on-beta ganglion cell. J. Neurosci. 8:1988;623-642.
52. J. Stone, The Wholemount Handbook, Sydney, Maitland Press, 1981.
53. Strettoi E., Dacheux R.F., Raviola E. Synaptic connections of rod bipolar cells in the inner plexiform layer of the rabbit retina. J. Comp. Neurol. 295:1990;449-466.
54. Strettoi E., Raviola E., Dacheux R.F. Synaptic connections of the narrow-field, bistratified rod amacrine cell (AII) in the rabbit retina. J. Comp. Neurol. 325:1992;152-168.
55. Turner D.L., Cepko C.L. A common progenitor for neurons and glia persists in rat retina late in development. Nature. 328:1987;131-136.
56. Uesugi R., Yamada M., Mizuguchi M., Baimbridge K.G., Kim S.U. Calbindin D-28 k and parvalbumin immunohistochemistry in developing rat retina. Exp. Eye Res. 54:1992;491-499.
57. Vaney D.I., Gynther I.C., Young H.M. Rod-signal interneurons in the rabbit retina: 2. AII amacrine cells. J. Comp. Neurol. 310:1991;154-169.
58. Vaney D.I., Young H.M., Gynther I.C. The rod circuit in the rabbit retina. Vis. Neurosci. 7:1991;141-154.
59. Voigt T., Wässle H. Dopaminergic innervation of AII amacrine cells in mammalian retina. J. Neurosci. 7:1987;4115-4128.
60. Wässle H., Riemann H.J. The mosaic of nerve cells in the mammalian retina. Proc. R. Soc. Lond. (B). 200:1978;441-461.
61. Wässle H., Grünert U., Röhrenbeck J. Immunocytochemical staining of AII amacrine cells in the rat retina with antibodies against parvalbumin. J. Comp. Neurol. 332:1993;407-420.
62. Wässle H., Grünert U., Chun M.-H., Boycott B.B. The rod pathway of the macaque monkey retina: Identification of AII-amacrine cells with antibodies against calretinin. J. Comp. Neurol. 361:1995;537-551.
63. Wikler K.C., Rakic P. Relation of an array of early-differentiating cones to the photoreceptor mosaic in the primate retina. Nature. 351:1991;397-400.
64. Wong R.O.L. Effects of glutamate and its analogs on intracellular calcium levels in the developing retina. Vis. Neurosci. 12:1995;907-917.
65. Young H.M., Vaney D.I. Rod-signal interneurons in the rabbit retina: 1. Rod bipolar cells. J. Comp. Neurol. 310:1991;139-153.