Differential immunodetection of l-DOPA decarboxylase and tyrosine hydroxylase in the vertebrate retina

International Journal of Developmental Neuroscience

Volumn 27, Issue 5, 2009, Pages 469-476

  Taveira da Silva, Rosilane ^a   Hokoç, Jan Nora ^a   de Mello, Fernando Garcia ^a   Gardino, Patrícia Franca ^a  

^a FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

Author keywords

Avian; Dopaminergic activity; Mammals; Retina development

Indexed keywords

AROMATIC LEVO AMINO ACID DECARBOXYLASE; DOPAMINE; TYROSINE 3 MONOOXYGENASE;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DENSITY; CELL LABELING; CONTROLLED STUDY; DEVELOPMENTAL STAGE; DOPAMINE METABOLISM; EMBRYO; EMBRYO DEVELOPMENT; ENZYME LOCALIZATION; FEMALE; IMMUNODETECTION; MALE; NONHUMAN; OPOSSUM; PRIORITY JOURNAL; RAT; RETINA CELL;

ANIMALS; CHICK EMBRYO; DIDELPHIS; DOPA DECARBOXYLASE; FEMALE; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; MALE; MICROSCOPY, CONFOCAL; RATS; RETINA; TYROSINE 3-MONOOXYGENASE;

AVES; DIDELPHIDAE; MAMMALIA; RATTUS; VERTEBRATA;

EID: 67349273637     PISSN: 07365748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijdevneu.2009.05.003     Document Type: Article

References (33)

1. Berger B., Verney C., Alvarez C., Vigny A., and Helle K.B. New dopaminergic terminal fields in the motor, visual (area 18b) and retrosplenial cortex in the young and adult rat. Immunocytochemical and catecholamine histochemical analyses. Neuroscience 15 (1985) 983-998
2. Borba J.C., Henze I.P., Silveira M.S., Kubrusly R.C., Gardino P.F., De Mello M.C., Hokoç J.N., and De Mello F.G. Pituitary adenylate cyclase-activating polypeptide (PACAP) can act as determinant of the tyrosine hydroxylase phenotype of dopaminergic cells during retina development. Developmental Brain Research 156 (2005) 193-201
3. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72 (1976) 248-254
4. De Mello F.G. The ontogeny of dopamine-dependent increase of adenosine 3′, 5′-cyclic monophosphate in the chick retina. Journal of Neurochemistry 31 (1978) 1049-1053
5. De Melo Reis R.A., Ventura A.L., Schitine C.S., de Mello M.C., and de Mello F.G. Müller glia as an active compartment modulating nervous activity in the vertebrate retina: neurotransmitters and trophic factors. Neurochemical Research 33 (2008) 1466-1474
6. Dos Santos R.M., and Gardino P.F. Differential distribution of a second type of tyrosine hydroxylase immunoreactive amacrine cell in the chick retina. Journal of Neurocytology 27 (1998) 33-43
7. Gardino P.F., Dos Santos R.M., and Hokoc J.N. Histogenesis and topographical distribution of tyrosine hydroxylase immunoreactive amacrine cells in the developing chick retina. Developmental Brain Research 72 (1993) 226-236
8. Guimarães M.Z., Hokoc J.N., Duvoisin R., Reis R.A., and De Mello F.G. Dopaminergic retinal cell differentiation in culture: modulation by forskolin and dopamine. European Journal of Neuroscience 13 (2001) 1931-1937
9. Hamburguer V., and Hamilton H.L. A series of normal stages in the development of the chick embryo. Journal of Morphology 88 (1951) 49-92
10. Ilia M., and Jeffery G. Retinal cell addition and rod production depend on early stages of ocular melanin synthesis. Journal of Comparative Neurology 420 (2000) 437-444
11. Izumi Y., Hammerman S.B., Benz A.M., Labruyere J., Zorumski C.F., and Olney J.W. Comparison of rat retinal fixation techniques: chemical fixation and microwave irradiation. Experimental Eye Research 70 (2000) 191-198
12. Jaeger C.B., and Joh T.H. Transient expression of tyrosine hydroxylase in some neurons of the developing inferior colliculus of the rat. Brain Research 313 (1983) 128-132
13. Kagami H., Sakai H., Uryu K., Kaneda T., and Sakanaka M. Development of tyrosine hydroxylase-like immunoreactive structures in the chick retina: three-dimensional analysis. Journal of Comparative Neurology 308 (1991) 356-370
14. Jeffery G., Brem G., and Montoliu L. Correction of retinal abnormalities found in albinism by introduction of a functional tyrosinase gene in transgenic mice and rabbits. Brain Research Developmental Brain Research 99 (1997) 95-102
15. Jeffery G. The retinal pigment epithelium as a developmental regulator of the neural retina. Eye 12 (1998) 499-503
16. Kato S., Negishi K., and Teranishi T. Embryonic development of monoaminergic neurons in the chick retina. Journal of Comparative Neurology 224 (1984) 437-444
17. Kojima A., Nakahama K., Ohno-Matsui K., Shimada N., Mori K., Iseki S., Sato T., Mochizuki M., and Morita I. Connexin-43 contributes to differentiation of retinal epithelial cells via cyclic AMP signaling. Biochemical and Biophysical Research Communications 366 (2007) 532-538
18. Kralj-Hans I., Tibber M., Jeffery G., and Mobbs P. Differential effect of dopamine on mitosis in early postnatal albino and pigmented rat retinae. Journal of Neurobiology 66 (2006) 47-55
19. Kubrusly R.C., Guimarães M.Z., Vieira A.P., Hokoc J.N., Casarini D.E., De Mello M.C., and De Mello F.G. l-DOPA supply to the neuro retina activates dopaminergic communication at the early stages of embryonic development. Journal of Neurochemistry 86 (2003) 45-54
20. Kubrusly R.C., Panizzutti R., Gardino P.F., Stutz B., Reis R.A., Ventura A.L., de Mello M.C., and de Mello F.G. Expression of functional dopaminergic phenotype in purified cultured Müller cells from vertebrate retina. Neurochemical International 53 (2008) 63-70
21. Lankford K.L., De Mello F.G., and Klein W.L. D1-type dopamine receptors inhibit growth cone motility in cultured retina neurons: evidence that neurotransmitters act as morphogenic growth regulators in the developing central nervous system. Proceedings of the National Academy of Sciences of the United States of America 85 (1988) 2839-2843
22. Lavado A., Jeffery G., Tovar V., de la Villa P., and Montoliu L. Ectopic expression of tyrosine hydroxylase in the pigmented epithelium rescues the retinal abnormalities and visual function common in albinos in the absence of melanin. Journal of Neurochemistry 96 (2006) 1201-1211
23. Naash M.I., Ripps H., Li S., Goto Y., and Peachey N.S. Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice. Journal of Neuroscience 16 (1996) 7853-7858
24. Nagatsu I., Sakai M., Takeuchi T., Arai R., Karasawa N., Yamada K., and Nagatsu T. Tyrosine hydroxylase (TH)-only-immunoreactive non-catecholaminergic neurons in the brain of wild mice or the human TH transgenic mice do not contain GTP cyclohydrolase I. Neuroscience Letters 228 (1997) 55-57
25. Page-Mccaw P., Chung S.C., Muto A., Roeser T., Staub W., Finger-Baier K.C., Korenbrot J.I., and Baier H. Retinal network adaptation to bright light requires tyrosinase. Nature Neuroscience 7 (2004) 1329-1336
26. Soares H.C., De Melo Reis R.A., De Mello F.G., Ventura A.L., and Kurtenbach E. Differential expression of D (1A) and D (1B) dopamine receptor mRNAs in the developing retina. Journal of Neurochemistry 75 (2000) 1071-1075
27. Summers C.G. Vision in albinism. Transactions of the American Ophthalmological Society 94 (1996) 1095-1155
28. Teakle E.M., Wildsoet C.F., and Vaney D.I. The spatial organization of tyrosine hydroxylase-immunoreactive amacrine cells in the chicken retina and the consequences of myopia. Vision Research 33 (1993) 2383-2396
29. Tibber M.S., Becker D., and Jeffery G. Levels of transient gap junctions between the retinal pigment epithelium and the neuroblastic retina are influenced by catecholamines and correlate with patterns of cell production. Journal of Comparative Neurology 503 (2007) 128-134
30. Tibber M.S., Whitmore A.V., and Jeffery G. Cell division and cleavage orientation in the developing retina are regulated by l-DOPA. Journal of Comparative Neurology 496 (2006) 369-381
31. Ventura A.L., Klein W.L., and De Mello F.G. Differential ontogenesis of D1 and D2 dopaminergic receptors in the chick embryo retina. Brain Research 314 (1984) 217-223
32. Versaux-Botteri C., Nguyen-Legros J., Vigny A., and Raoux N. Morphology, density and distribution of tyrosine hydroxylase-like immunoreactive cells in the retina of mice. Brain Research 301 (1984) 192-197
33. Wang H.H., Cuenca N., and Kolb H. Development of morphological types and distribution patterns of amacrine cells immunoreactive to tyrosine hydroxylase in the cat retina. Vision Neuroscience 4 (1990) 159-175