Creb is modulated in the mouse superior colliculus in developmental and experimentally-induced models of plasticity

International Journal of Developmental Neuroscience

Volumn 31, Issue 1, 2013, Pages 46-52

  Vierci, Gabriela ^a   Oliveira, Camila Salum De ^b,d   Perera, Lucia Ruiz ^a   Bornia, Natalia ^a   Leal, Rodrigo Bainy ^b   Rossi, Francesco Mattia ^a,c  

^a UNIVERSIDAD DE LA REPÚBLICA   (Uruguay)

^b FEDERAL UNIVERSITY OF SANTA CATARINA   (Brazil)

^c INSTITUT PASTEUR DE MONTEVIDEO   (Uruguay)

^d UNIVERSITY OF NEWCASTLE   (Australia)

Author keywords

CREB; Mouse; Neuronal plasticity; Phospho CREB; Superior colliculus

Indexed keywords

CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN; FLUOXETINE; PROTEIN ANTIBODY;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN DAMAGE; BRAIN DEVELOPMENT; CONTROLLED STUDY; INTRACELLULAR SIGNALING; MOUSE; NERVE CELL PLASTICITY; NEUROMODULATION; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; SUPERIOR COLLICULUS; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION; VISUAL CORTEX; WESTERN BLOTTING;

AGE FACTORS; ANALYSIS OF VARIANCE; ANIMALS; ANIMALS, NEWBORN; CREB-BINDING PROTEIN; DENSITOMETRY; EYE ENUCLEATION; FLUOXETINE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; NEURONAL PLASTICITY; SERINE; SEROTONIN UPTAKE INHIBITORS; SUPERIOR COLLICULI; VISUAL PATHWAYS;

ANIMALIA; MUS;

EID: 84870489219     PISSN: 07365748     EISSN: 1873474X     Source Type: Journal    
DOI: 10.1016/j.ijdevneu.2012.10.003     Document Type: Article

References (58)

1. Baroncelli L., Braschi C., Spolidoro M., Begenisic T., Sale A., Maffei L. Nurturing brain plasticity: impact of environmental enrichment. Cell Death and Differentiation 2010, 17:1092-1103.
2. Bastos E.F., Marcelino J.L., Amaral A.R., Serfaty C.A. Fluoxetine-induced plasticity in the rodent visual system. Brain Research 1999, 824:28-35.
3. Benito E., Barco A. CREB's control of intrinsic and synaptic plasticity: implications for CREB-dependent memory models. Trends in Neurosciences 2010, 33:230-240.
4. Brindle P.K., Montminy M.R. The CREB family of transcription activators. Current Opinion in Genetics and Development 1992, 2:199-204.
5. Campello-Costa P., Fosse A.M., Ribeiro J.C., Paes-De-Carvalho R., Serfaty C.A. Acute blockade of nitric oxide synthesis induces disorganization and amplifies lesion-induced plasticity in the rat retinotectal projection. Journal of Neurobiology 2000, 44:371-381.
6. Carlezon W.A., Duman R.S., Nestler E.J. The many faces of CREB. Trends in Neurosciences 2005, 28:436-445.
7. Castrén E., Rantamäki T. The role of BDNF and its receptors in depression and antidepressant drug action: reactivation of developmental plasticity. Developmental Neurobiology 2010, 70:289-297.
8. Chalupa L.M., Henderson Z. Monocular enucleation in adult hamsters induces functional changes in the remaining ipsilateral retinotectal projection. Brain Research 1980, 192:249-254.
9. Chen J.L., Lin W.C., Cha J.W., So P.T., Kubota Y., Nedivi E. Structural basis for the role of inhibition in facilitating adult brain plasticity. Nature Neuroscience 2011, 14:587-594.
10. Di Cristo G., Berardi N., Cancedda L., Pizzorusso T., Putignano E., Ratto G.M., Maffei L. Requirement of ERK activation for visual cortical plasticity. Science 2001, 292:2337-2340.
11. Dulawa S.C., Holick K.A., Gundersen B., Hen R. Effects of chronic fluoxetine in animal models of anxiety and depression. Neuropsychopharmacology 2004, 29:1321-1330.
12. Fawcett J.W., O'Leary D.D., Cowan W.M. Activity and the control of ganglion cell death in the rat retina. Proceedings of the National Academy of Sciences of the United States of America 1984, 81:5589-5593.
13. Feldheim D.A., O'Leary D.D. Visual map development: bidirectional signaling, bifunctional guidance molecules, and competition. Cold Spring Harbor Perspectives in Biology 2010, 2:a001768.
14. Frost D.O., Schneider G.E. Plasticity of retinofugal projections after partial lesions of the retina in newborn Syrian hamsters. Journal of Comparative Neurology 1979, 185:517-567.
15. Gau D., Lemberger T., von Gall C., Kretz O., Le Minh N., Gass P., Schmid W., Schibler U., Korf H.W., Schütz G. Phosphorylation of CREB Ser142 regulates light-induced phase shifts of the circadian clock. Neuron 2002, 34:245-253.
16. Godement P., Saillour P., Imbert M. The ipsilateral optic pathway to the dorsal lateral geniculate nucleus and superior colliculus in mice with prenatal or postnatal loss of one eye. Journal of Comparative Neurology 1980, 190:611-626.
17. Godement P., Salaun J., Imbert M. Prenatal and postnatal development of retinogeniculate and retino-collicular projections in the mouse. Journal of Comparative Neurology 1984, 230:552-575.
18. Hahm J.O., Langdon R.B., Sur M. Disruption of retinogeniculate afferent segregation by antagonists to NMDA receptors. Nature 1991, 351:568-570.
19. Hammer Ø., Harper D.A.T., Ryan P.D. PAST: paleontological statistics software package for education and data analysis. Palaeontologia Electronica 2001, 4(1):9. http://palaeo-electronica.org/2001_1/past/issue1_01.htm.
20. Johannessen M., Delghandi M.P., Moens U. What turns CREB on?. Cellular Signalling 2004, 16:1211-1227.
21. Karpova N.N., Lindholm J., Pruunsild P., Timmusk T., Castrén E. Long-lasting behavioural and molecular alterations induced by early postnatal fluoxetine exposure are restored by chronic fluoxetine treatment in adult mice. European Neuropsychopharmacology 2009, 19:97-108.
22. Katoh-Semba R., Tsuzuki M., Miyazaki N., Matsuda M., Nakagawa C., Ichisaka S., Sudo K., Kitajima S., Hamatake M., Hata Y., Nagata K. A phase advance of the light-dark cycle stimulates production of BDNF, but not of other neurotrophins, in the adult rat cerebral cortex: association with the activation of CREB. Journal of Neurochemistry 2008, 106:2131-2142.
23. Katz L.C., Shatz C.J. Synaptic activity and the construction of cortical circuits. Science 1996, 274:1133-1138.
24. Krahe T.E., Seabrook T.A., Chen C.K., Fox M.A., Guido W. Modulation of CREB in the dorsal lateral geniculate nucleus of dark-reared mice. Neural Plasticity 2012, 2012:426437.
25. Lalonde J., Chaudhuri A. Dynamic changes in CREB phosphorylation and neuroadaptive gene expression in area V1 of adult monkeys after monocular enucleation. Molecular and Cellular Neurosciences 2007, 35:24-37.
26. Land P.W., Lund R.D. Development of the rat's uncrossed retinotectal pathway and its relation to plasticity studies. Science 1979, 205:698-700.
27. Levelt C.N., Hübener M. Critical-period plasticity in the visual cortex. Annual Review of Neuroscience 2012, 35:309-330.
28. Lund R.D., Lund J.S. Plasticity in the developing visual system: the effects of retinal lesions made in young rats. Journal of Comparative Neurology 1976, 169:133-154.
29. Maya-Vetencourt J.F., Sale A., Viegi A., Baroncelli L., De Pasquale R., O'Leary O.F., Castrén E., Maffei L. The antidepressant fluoxetine restores plasticity in the adult visual cortex. Science 2008, 320:385-388.
30. McClung C.A., Nestler E.J. Neuroplasticity mediated by altered gene expression. Neuropsychopharmacology 2008, 33:3-17.
31. Mo Z., Suneja S.K., Potashner S.J. Phosphorylated cAMP response element-binding protein levels in guinea pig brainstem auditory nuclei after unilateral cochlear ablation. Journal of Neuroscience Research 2006, 83:1323-1330.
32. Mower A.F., Liao D.S., Nestler E.J., Neve R.L., Ramoa A.S. cAMP/Ca2+ response element-binding protein function is essential for ocular dominance plasticity. Journal of Neuroscience 2002, 22:2237-2245.
33. Naska S., Cenni M.C., Menna E., Maffei L. ERK signaling is required for eye-specific retino-geniculate segregation. Development 2004, 131:3559-3570.
34. Obata S., Obata J., Das A., Gilbert C.D. Molecular correlates of topographic reorganization in primary visual cortex following retinal lesions. Cerebral Cortex 1999, 9:238-248.
35. Obrietan K., Impey S., Smith D., Athos J., Storm D.R. Circadian regulation of cAMP response element-mediated gene expression in the suprachiasmatic nuclei. Journal of Biological Chemistry 1999, 274:17748-17756.
36. Oliveira C.S., Rigon A.P., Leal R.B., Rossi F.M. The activation of ERK1/2 and p38 mitogen-activated protein kinases is dynamically regulated in the developing rat visual system. International Journal of Developmental Neuroscience 2008, 26:355-362.
37. Oliveira-Silva P., Jurgilas P.B., Trindade P., Campello-Costa P., Perales J., Savino W., Serfaty C.A. Matrix metalloproteinase-9 is involved in the development and plasticity of retinotectal projections in rats. Neuroimmunomodulation 2007, 14:144-149.
38. Parker D., Jhala U.S., Radhakrishnan I., Yaffe M.B., Reyes C., Shulman A.I., Cantley L.C., Wright P.E., Montminy M. Analysis of an activator: coactivator complex reveals an essential role for secondary structure in transcriptional activation. Molecular Cell 1998, 2:353-359.
39. Pham T.A., Impey S., Storm D.R., Stryker M.P. CRE-mediated gene transcription in neocortical neuronal plasticity during the developmental critical period. Neuron 1999, 22:63-72.
40. Pham T.A., Rubenstein J.L., Silva A.J., Storm D.R., Stryker M.P. The CRE/CREB pathway is transiently expressed in thalamic circuit development and contributes to refinement of retinogeniculate axons. Neuron 2001, 31:409-420.
41. Pham T.A., Graham S.J., Suzuki S., Barco A., Kandel E.R., Gordon B., Lickey M.E. A semi-persistent adult ocular dominance plasticity in visual cortex is stabilized by activated CREB. Learning and Memory 2004, 11:738-747.
42. Rantamäki T., Hendolin P., Kankaanpää A., Mijatovic J., Piepponen P., Domenici E., Chao M.V., Männistö P.T., Castrén E. Pharmacologically diverse antidepressants rapidly activate brain-derived neurotrophic factor receptor TrkB and induce phospholipase-Cgamma signaling pathways in mouse brain. Neuropsychopharmacology 2007, 32:2152-2162.
43. Ravary A., Muzerelle A., Hervé D., Pascoli V., Ba-Charvet K.N., Girault J.A., Welker E., Gaspar P. Adenylate cyclase 1 as a key actor in the refinement of retinal projection maps. Journal of Neuroscience 2003, 23:2228-2238.
44. Rossi F.M., Sala R., Maffei L. Expression of the nerve growth factor receptors TrkA and p75NTR in the visual cortex of the rat: development and regulation by the cholinergic input. Journal of Neuroscience 2002, 22:912-919.
45. Sakamoto K., Karelina K., Obrietan K. CREB: a multifaceted regulator of neuronal plasticity and protection. Journal of Neurochemistry 2011, 116:1-9.
46. Sale A., Berardi N., Maffei L. Enrich the environment to empower the brain. Trends in Neurosciences 2009, 32:233-239.
47. Sassone-Corsi P. Transcription factors responsive to cAMP. Annual Review of Cell and Developmental Biology 1995, 11:355-377.
48. Serfaty C.A., Campello-Costa P., Linden R. Rapid and long-term plasticity in the neonatal and adult retinotectal pathways following a retinal lesion. Brain Research Bulletin 2005, 66:128-134.
49. Shatz C.J., Stryker M.P. Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents. Science 1988, 242:87-89.
50. Sretavan D.W., Shatz C.J., Stryker M.P. Modification of retinal ganglion cell axon morphology by prenatal infusion of tetrodotoxin. Nature 1988, 336:468-471.
51. Tardito D., Perez J., Tiraboschi E., Musazzi L., Racagni G., Popoli M. Signaling pathways regulating gene expression, neuroplasticity, and neurotrophic mechanisms in the action of antidepressants: a critical overview. Pharmacological Reviews 2006, 58:115-134.
52. Tavares Gomes A.L., Maia F.B., Oliveira-Silva P., Marques Ventura A.L., Paes-De-Carvalho R., Serfaty C.A., Campello-Costa P. Purinergic modulation in the development of the rat uncrossed retinotectal pathway. Neuroscience 2009, 163:1061-1068.
53. Thome J., Sakai N., Shin K., Steffen C., Zhang Y.J., Impey S., Storm D., Duman R.S. cAMP response element-mediated gene transcription is upregulated by chronic antidepressant treatment. Journal of Neuroscience 2000, 20:4030-4036.
54. Tiraboschi E., Tardito D., Kasahara J., Moraschi S., Pruneri P., Gennarelli M., Racagni G., Popoli M. Selective phosphorylation of nuclear CREB by fluoxetine is linked to activation of CaM kinase IV and MAP kinase cascades. Neuropsychopharmacology 2004, 29:1831-1840.
55. Tropea D., Caleo M., Maffei L. Synergistic effects of brain-derived neurotrophic factor and chondroitinase ABC on retinal fiber sprouting after denervation of the superior colliculus in adult rats. Journal of Neuroscience 2003, 23:7034-7044.
56. Upton A.L., Salichon N., Lebrand C., Ravary A., Blakely R., Seif I., Gaspar P. Excess of serotonin (5-HT) alters the segregation of ispilateral and contralateral retinal projections in monoamine oxidase A knock-out mice: possible role of 5-HT uptake in retinal ganglion cells during development. Journal of Neuroscience 1999, 19:7007-7024.
57. Vercelli A., Garbossa D., Biasiol S., Repici M., Jhaveri S. NOS inhibition during postnatal development leads to increased ipsilateral retino-collicular and retinogeniculate projections in rats. European Journal of Neuroscience 2000, 12:473-490.
58. Wu X., McMurray C.T. Calmodulin kinase II attenuation of gene transcription by preventing cAMP response element-binding protein (CREB) dimerization and binding of the CREB-binding protein. Journal of Biological Chemistry 2001, 276:1735-1741.