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      Experience-dependent expression of Nogo-A and Nogo receptor in the developing rat visual cortex

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          Abstract

          Nogo-A and Nogo receptor (NgR) expression in the visual cortex following a critical developmental period (postnatal days 20–60) has been previously shown. However, little is known regarding Nogo-A and NgR expression between postnatal day 0 and initiation of the critical period. The present study analyzed Nogo-A and NgR expression at four different time points: postnatal day 0 (P0), before critical period (P14), during critical period (P28), and after critical period (P60). Results showed significantly increased Nogo-A mRNA and protein expression levels in the visual cortex following birth, and expression levels remained steady between P28 and P60. NgR mRNA or protein expression was dramatically upregulated with age and peaked at P14 or P28, respectively, and maintained high expression to P60. In addition, Nogo-A and NgR expression was analyzed in each visual cortex layer in normal developing rats and rats with monocular deprivation. Monocular deprivation decreased Nogo-A and NgR mRNA and protein expression in the rat visual cortex, in particular in layers II-III and IV in the visual cortex contralateral to the deprived eye. These findings suggested that Nogo-A and NgR regulated termination of the critical period in experience- dependent visual cortical plasticity.

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          Most cited references17

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          SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE.

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            Experience-dependent plasticity of binocular responses in the primary visual cortex of the mouse.

            An activity-dependent form of synaptic plasticity underlies the fine tuning of connections in the developing primary visual cortex of mammals such as the cat and monkey. Studies of the effects of manipulations of visual experience during a critical period have demonstrated that a correlation-based competitive process governs this plasticity. The cellular mechanisms underlying this competition, however, are poorly understood. Transgenic and gene-targeting technologies have led to the development of a new category of reagents that have the potential to help answer questions of cellular mechanism, provided that the questions can be studied in a mouse model. The current study attempts to characterize a developmental plasticity in the mouse primary visual cortex and to demonstrate its relevance to that found in higher mammals. We found that 4 d of monocular lid suture at postnatal day 28 (P28) induced a maximal loss of responsiveness of cortical neurons to the deprived eye. These ocular dominance shifts occurred during a well-defined critical period, between P19 and P32. Furthermore, binocular deprivation during this critical period did not decrease visual cortical responses, and alternating monocular deprivation resulted in a decrease in the number of binocularly responsive neurons. Finally, a laminar analysis demonstrated plasticity of both geniculocortical and intracortical connections. These results demonstrate that an activity-dependent, competitive form of synaptic plasticity that obeys correlation-based rules operates in the developing primary visual cortex of the mouse.
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              LINGO-1 is a component of the Nogo-66 receptor/p75 signaling complex.

              Axon regeneration in the adult CNS is prevented by inhibitors in myelin. These inhibitors seem to modulate RhoA activity by binding to a receptor complex comprising a ligand-binding subunit (the Nogo-66 receptor NgR1) and a signal transducing subunit (the neurotrophin receptor p75). However, in reconstituted non-neuronal systems, NgR1 and p75 together are unable to activate RhoA, suggesting that additional components of the receptor may exist. Here we describe LINGO-1, a nervous system-specific transmembrane protein that binds NgR1 and p75 and that is an additional functional component of the NgR1/p75 signaling complex. In non-neuronal cells, coexpression of human NgR1, p75 and LINGO-1 conferred responsiveness to oligodendrocyte myelin glycoprotein, as measured by RhoA activation. A dominant-negative human LINGO-1 construct attenuated myelin inhibition in transfected primary neuronal cultures. This effect on neurons was mimicked using an exogenously added human LINGO-1-Fc fusion protein. Together these observations suggest that LINGO-1 has an important role in CNS biology.
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                Author and article information

                Journal
                Neural Regen Res
                Neural Regen Res
                NRR
                Neural Regeneration Research
                Medknow Publications & Media Pvt Ltd (India )
                1673-5374
                1876-7958
                05 January 2012
                : 7
                : 1
                : 13-17
                Affiliations
                [1] Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China
                Author notes

                Xiaoying Wu, Professor, Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China

                Corresponding author: Xiaoying Wu, Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China wux-iaoyingxy@ 123456yahoo.cn (N20110225002/WLM)

                Author contributions: Xiaoying Wu, Yulin Luo, and Shuangzhen Liu designed the study; Yulin Luo and Kuanshu Li performed the experiments; Yulin Luo and Xiaoying Wu analyzed the data; Yulin Luo and Xiaoying Wu wrote the manuscript.

                Article
                NRR-7-13
                10.3969/j.issn.1673-5374.2012.01.002
                4354109
                1cf5e8fc-68d7-4fe5-9f9c-a45a5a251217
                Copyright: © Neural Regeneration Research

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 May 2011
                : 12 July 2011
                Categories
                Research and Report: Neurogensis and Neural Plasticicty

                monocular deprivation,neural regeneration,nogo receptor,nogo-a,plasticity,primary visual cortex

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