Molecular development of the lateral geniculate nucleus in the absence of retinal waves during the time of retinal axon eye-specific segregation

Neuroscience

Volumn 159, Issue 4, 2009, Pages 1326-1337

  Iwai, L ^a,b   Kawasaki, H ^a,b,c  

^a UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

ferret; mouse; PCP4; spontaneous activity; TCF7L2; visual system

Indexed keywords

CELL PROTEIN; CLORGYLINE; EPIBATIDINE; LIM HOMEOBOX PROTEIN 9; NUCLEIC ACID BINDING PROTEIN; PURKINJE CELL PROTEIN 4; TRANSCRIPTION FACTOR 7 LIKE 2; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CONTROLLED STUDY; FERRET; IN VIVO STUDY; LATERAL GENICULATE NUCLEUS; MALE; NONHUMAN; PRIORITY JOURNAL; RETINA;

ANIMALS; ANIMALS, NEWBORN; BICYCLO COMPOUNDS, HETEROCYCLIC; CLORGYLINE; EYE ENUCLEATION; FERRETS; GENICULATE BODIES; HOMEODOMAIN PROTEINS; LYMPHOID ENHANCER-BINDING FACTOR 1; MICE; MICE, INBRED C57BL; MONOAMINE OXIDASE INHIBITORS; NERVE TISSUE PROTEINS; NICOTINIC AGONISTS; PYRIDINES; RETINA; RETINAL NEURONS; TCF TRANSCRIPTION FACTORS; VISUAL PATHWAYS;

EID: 63349087017     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2009.02.010     Document Type: Article

References (53)

1. Arce L., Yokoyama N.N., and Waterman M.L. Diversity of LEF/TCF action in development and disease. Oncogene 25 (2006) 7492-7504
2. Bansal A., Singer J.H., Hwang B.J., Xu W., Beaudet A., and 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
3. Bjartmar L., Huberman A.D., Ullian E.M., Renteria R.C., Liu X., Xu W., Prezioso J., Susman M.W., Stellwagen D., Stokes C.C., Cho R., Worley P., Malenka R.C., Ball S., Peachey N.S., Copenhagen D., Chapman B., Nakamoto M., Barres B.A., and Perin M.S. Neuronal pentraxins mediate synaptic refinement in the developing visual system. J Neurosci 26 (2006) 6269-6281
4. Boulanger L.M., and Shatz C.J. Immune signalling in neural development, synaptic plasticity and disease. Nat Rev Neurosci 5 (2004) 521-531
5. Bribian A., Barallobre M.J., Soussi-Yanicostas N., and de Castro F. Anosmin-1 modulates the FGF-2-dependent migration of oligodendrocyte precursors in the developing optic nerve. Mol Cell Neurosci 33 (2006) 2-14
6. Cases O., Vitalis T., Seif I., De Maeyer E., Sotelo C., and Gaspar P. Lack of barrels in the somatosensory cortex of monoamine oxidase A-deficient mice: role of a serotonin excess during the critical period. Neuron 16 (1996) 297-307
7. Corriveau R.A., Huh G.S., and Shatz C.J. Regulation of class I MHC gene expression in the developing and mature CNS by neural activity. Neuron 21 (1998) 505-520
8. Crowley J.C., and Katz L.C. Development of ocular dominance columns in the absence of retinal input. Nat Neurosci 2 (1999) 1125-1130
9. Erhardt J.A., Legos J.J., Johanson R.A., Slemmon J.R., and Wang X. Expression of PEP-19 inhibits apoptosis in PC12 cells. Neuroreport 11 (2000) 3719-3723
10. Feller M.B., Wellis D.P., Stellwagen D., Werblin F.S., and Shatz C.J. Requirement for cholinergic synaptic transmission in the propagation of spontaneous retinal waves. Science 272 (1996) 1182-1187
11. Galli L., and Maffei L. Spontaneous impulse activity of rat retinal ganglion cells in prenatal life. Science 242 (1988) 90-91
12. Godement P., Salaun J., and Imbert M. Prenatal and postnatal development of retinogeniculate and retinocollicular projections in the mouse. J Comp Neurol 230 (1984) 552-575
13. Guillery R.W., LaMantia A.S., Robson J.A., and Huang K. The influence of retinal afferents upon the development of layers in the dorsal lateral geniculate nucleus of mustelids. J Neurosci 5 (1985) 1370-1379
14. Harada T., Morooka T., Ogawa S., and Nishida E. ERK induces p35, a neuron-specific activator of Cdk5, through induction of Egr1. Nat Cell Biol 3 (2001) 453-459
15. Heumann D., and Rabinowicz T. Postnatal development of the dorsal lateral geniculate nucleus in the normal and enucleated albino mouse. Exp Brain Res 38 (1980) 75-85
16. Hoppler S., and Kavanagh C.L. Wnt signalling: variety at the core. J Cell Sci 120 (2007) 385-393
17. Huberman A.D., Stellwagen D., and Chapman B. Decoupling eye-specific segregation from lamination in the lateral geniculate nucleus. J Neurosci 22 (2002) 9419-9429
18. Huh G.S., Boulanger L.M., Du H., Riquelme P.A., Brotz T.M., and Shatz C.J. Functional requirement for class I MHC in CNS development and plasticity. Science 290 (2000) 2155-2159
19. Jaubert-Miazza L., Green E., Lo F.S., Bui K., Mills J., and Guido W. Structural and functional composition of the developing retinogeniculate pathway in the mouse. Vis Neurosci 22 (2005) 661-676
20. Jessell T.M., and Dodd J. Structure and expression of differentiation antigens on functional subclasses of primary sensory neurons. Philos Trans R Soc Lond B Biol Sci 308 (1985) 271-281
21. Johanson R.A., Sarau H.M., Foley J.J., and Slemmon J.R. Calmodulin-binding peptide PEP-19 modulates activation of calmodulin kinase II in situ. J Neurosci 20 (2000) 2860-2866
22. Kawano H., Fukuda T., Kubo K., Horie M., Uyemura K., Takeuchi K., Osumi N., Eto K., and Kawamura K. Pax-6 is required for thalamocortical pathway formation in fetal rats. J Comp Neurol 408 (1999) 147-160
23. Kawasaki H., Crowley J.C., Livesey F.J., and Katz L.C. Molecular organization of the ferret visual thalamus. J Neurosci 24 (2004) 9962-9970
24. Kawasaki H., Fujii H., Gotoh Y., Morooka T., Shimohama S., Nishida E., and Hirano T. Requirement for mitogen-activated protein kinase in cerebellar long term depression. J Biol Chem 274 (1999) 13498-13502
25. Kawasaki H., Mizuseki K., Nishikawa S., Kaneko S., Kuwana Y., Nakanishi S., Nishikawa S.I., and Sasai Y. Induction of midbrain dopaminergic neurons from ES cells by stromal cell-derived inducing activity. Neuron 28 (2000) 31-40
26. Konur S., and Ghosh A. Calcium signaling and the control of dendritic development. Neuron 46 (2005) 401-405
27. Kunz M., Herrmann M., Wedlich D., and Gradl D. Autoregulation of canonical Wnt signaling controls midbrain development. Dev Biol 273 (2004) 390-401
28. Linden D.C., Guillery R.W., and Cucchiaro J. The dorsal lateral geniculate nucleus of the normal ferret and its postnatal development. J Comp Neurol 203 (1981) 189-211
29. Maffei L., and Galli-Resta L. Correlation in the discharges of neighboring rat retinal ganglion cells during prenatal life. Proc Natl Acad Sci U S A 87 (1990) 2861-2864
30. McAllister A.K., Lo D.C., and Katz L.C. Neurotrophins regulate dendritic growth in developing visual cortex. Neuron 15 (1995) 791-803
31. McLaughlin T., Torborg C.L., Feller M.B., and O'Leary D.D. Retinotopic map refinement requires spontaneous retinal waves during a brief critical period of development. Neuron 40 (2003) 1147-1160
32. Meister M., Wong R.O., Baylor D.A., and Shatz C.J. Synchronous bursts of action potentials in ganglion cells of the developing mammalian retina. Science 252 (1991) 939-943
33. Menna E., Cenni M.C., Naska S., and Maffei L. The anterogradely transported BDNF promotes retinal axon remodeling during eye specific segregation within the LGN. Mol Cell Neurosci 24 (2003) 972-983
34. Molle B., Pere S., Failli V., Bach I., and Retaux S. Lhx9 and lhx9alpha: differential biochemical properties and effects on neuronal differentiation. DNA Cell Biol 23 (2004) 761-768
35. Nakagawa Y., and O'Leary D.D. Combinatorial expression patterns of LIM-homeodomain and other regulatory genes parcellate developing thalamus. J Neurosci 21 (2001) 2711-2725
36. Naska S., Cenni M.C., Menna E., and Maffei L. ERK signaling is required for eye-specific retino-geniculate segregation. Development 131 (2004) 3559-3570
37. Penn A.A., Riquelme P.A., Feller M.B., and Shatz C.J. Competition in retinogeniculate patterning driven by spontaneous activity. Science 279 (1998) 2108-2112
38. Pham T.A., Rubenstein J.L., Silva A.J., Storm D.R., and Stryker M.P. The CRE/CREB pathway is transiently expressed in thalamic circuit development and contributes to refinement of retinogeniculate axons. Neuron 31 (2001) 409-420
39. Porter F.D., Drago J., Xu Y., Cheema S.S., Wassif C., Huang S.P., Lee E., Grinberg A., Massalas J.S., Bodine D., Alt F., and Westphal H. Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development. Development 124 (1997) 2935-2944
40. Pratt T., Vitalis T., Warren N., Edgar J.M., Mason J.O., and Price D.J. A role for Pax6 in the normal development of dorsal thalamus and its cortical connections. Development 127 (2000) 5167-5178
41. Ravary A., Muzerelle A., Herve D., Pascoli V., Ba-Charvet K.N., Girault J.A., Welker E., and Gaspar P. Adenylate cyclase 1 as a key actor in the refinement of retinal projection maps. J Neurosci 23 (2003) 2228-2238
42. Salichon N., Gaspar P., Upton A.L., Picaud S., Hanoun N., Hamon M., De Maeyer E., Murphy D.L., Mossner R., Lesch K.P., Hen R., and Seif I. Excessive activation of serotonin (5-HT) 1B receptors disrupts the formation of sensory maps in monoamine oxidase A and 5-HT transporter knock-out mice. J Neurosci 21 (2001) 884-896
43. Schmitt A.M., Shi J., Wolf A.M., Lu C.C., King L.A., and Zou Y. Wnt-Ryk signalling mediates medial-lateral retinotectal topographic mapping. Nature 439 (2006) 31-37
44. Shatz C.J. The prenatal development of the cat's retinogeniculate pathway. J Neurosci 3 (1983) 482-499
45. Shatz C.J., and Stryker M.P. Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents. Science 242 (1988) 87-89
46. Sherman S.M., and Guillery R.W. Thalamus. In: Shepherd G.M. (Ed). The synaptic organization of the brain (2004), Oxford University Press, New York 311-359
47. Slemmon J.R., Morgan J.I., Fullerton S.M., Danho W., Hilbush B.S., and Wengenack T.M. Camstatins are peptide antagonists of calmodulin based upon a conserved structural motif in PEP-19, neurogranin, and neuromodulin. J Biol Chem 271 (1996) 15911-15917
48. Sretavan D.W., and Shatz C.J. Prenatal development of retinal ganglion cell axons: segregation into eye-specific layers within the cat's lateral geniculate nucleus. J Neurosci 6 (1986) 234-251
49. Toda T., Hayakawa I., Matsubayashi Y., Tanaka K., Ikenaka K., Lu Q.R., and Kawasaki H. Termination of lesion-induced plasticity in the mouse barrel cortex in the absence of oligodendrocytes. Mol Cell Neurosci 39 (2008) 40-49
50. Torborg C.L., and Feller M.B. Spontaneous patterned retinal activity and the refinement of retinal projections. Prog Neurobiol 76 (2005) 213-235
51. Upton A.L., Salichon N., Lebrand C., Ravary A., Blakely R., Seif I., and 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. J Neurosci 19 (1999) 7007-7024
52. Wong R.O. Retinal waves and visual system development. Annu Rev Neurosci 22 (1999) 29-47
53. Wong R.O., Meister M., and Shatz C.J. Transient period of correlated bursting activity during development of the mammalian retina. Neuron 11 (1993) 923-938