Literature DB >> 10404257

Pattern formation by retinal afferents in the ferret lateral geniculate nucleus: developmental segregation and the role of N-methyl-D-aspartate receptors.

J O Hahm1, K S Cramer, M Sur.   

Abstract

The projection from the retina to the lateral geniculate nucleus (LGN) in ferrets segregates during development into eye-specific layers and ON/OFF sublayers. The projection pattern and the morphology of single axons was examined at several postnatal ages. The axons progress from a simple, sparsely branched morphology at birth to crude arbors at postnatal day 7 (P7). At P14-P15, axons have terminal arbors that span one eye-specific layer. By P19-P21, retinal afferents in the A layers have segregated into inner and outer sublaminae that correspond to ON- and OFF-center cells. Sublaminae form mainly by directed growth of terminal arbors in appropriately positioned regions of the LGN, along with elimination of extraneous branches in inappropriate regions. From P28 to P35, the LGN assumes an adult-like shape, and retinogeniculate axons form terminal boutons on branch endings. During the period between P14 and P21, when retinogeniculate axons segregate into ON/OFF sublaminae, N-methyl-D-aspartate (NMDA) receptors were blocked with chronic infusion of specific antagonists into the LGN. NMDA receptor blockade prevents the retinal afferent segregation into ON/OFF sublaminae. Some individual retinogeniculate axons have arbors that are not restricted appropriately, and most are restricted in size but are located inappropriately within the eye-specific laminae. Thus, NMDA receptor blockade prevents the positioning of retinogeniculate arbors that lead to the formation of ON/OFF sublaminae in the LGN. These results indicate that the activity of postsynaptic cells, and the activation of NMDA receptors in particular, can influence significantly the patterning of inputs and the structure of presynaptic afferents during development. Copyright 1999 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10404257     DOI: 10.1002/(sici)1096-9861(19990823)411:2<327::aid-cne12>3.0.co;2-#

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  18 in total

1.  Developmental changes in the neurotransmitter regulation of correlated spontaneous retinal activity.

Authors:  W T Wong; K L Myhr; E D Miller; R O Wong
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

2.  Activity-dependent patterning of retinogeniculate axons proceeds with a constant contribution from AMPA and NMDA receptors.

Authors:  C D Hohnke; S Oray; M Sur
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

3.  Decoupling eye-specific segregation from lamination in the lateral geniculate nucleus.

Authors:  Andrew D Huberman; David Stellwagen; Barbara Chapman
Journal:  J Neurosci       Date:  2002-11-01       Impact factor: 6.167

4.  Disruption of retinogeniculate pattern formation by inhibition of soluble guanylyl cyclase.

Authors:  C A Leamey; C L Ho-Pao; M Sur
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

5.  Activity dependence of cortical axon branch formation: a morphological and electrophysiological study using organotypic slice cultures.

Authors:  Naofumi Uesaka; Satoshi Hirai; Takuro Maruyama; Edward S Ruthazer; Nobuhiko Yamamoto
Journal:  J Neurosci       Date:  2005-01-05       Impact factor: 6.167

6.  Ephrin-As mediate targeting of eye-specific projections to the lateral geniculate nucleus.

Authors:  Andrew D Huberman; Karl D Murray; David K Warland; David A Feldheim; Barbara Chapman
Journal:  Nat Neurosci       Date:  2005-07-17       Impact factor: 24.884

7.  Increasing Spontaneous Retinal Activity before Eye Opening Accelerates the Development of Geniculate Receptive Fields.

Authors:  Zachary W Davis; Barbara Chapman; Hwai-Jong Cheng
Journal:  J Neurosci       Date:  2015-10-28       Impact factor: 6.167

8.  Rearrangement of retinogeniculate projection patterns after eye-specific segregation in mice.

Authors:  Itaru Hayakawa; Hiroshi Kawasaki
Journal:  PLoS One       Date:  2010-06-08       Impact factor: 3.240

9.  Orexin-A and orexin-B during the postnatal development of the rat brain.

Authors:  Irina I Stoyanova; Wim L C Rutten; Joost le Feber
Journal:  Cell Mol Neurobiol       Date:  2009-07-25       Impact factor: 5.046

10.  Hardwiring of fine synaptic layers in the zebrafish visual pathway.

Authors:  Linda M Nevin; Michael R Taylor; Herwig Baier
Journal:  Neural Dev       Date:  2008-12-16       Impact factor: 3.842

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.