Abstract
We investigated expression of the Nogo receptor (NgR) in the retina of rats between postnatal day 0 (PND 0) and adulthood (PND 63). Frozen sections of eyeball were prepared from each of six rats on PND 0, PND 3, PND 7, PND 14, PND 21, PND 35, PND 49, and PND 63. Immunofluorescence–histochemistry and laser-confocal microscopy were used to observe the expression of NgR protein. NgR is positive in the retina at all stages. It was distributed around ganglion cell nuclei and disposed linearly in the optic nerve. The NgR was expressed in rat retina at the time of birth and was present throughout postnatal development.
Similar content being viewed by others
References
Ye J, Wang ZG, Zhu PF, et al. Expressive varieties of Nogo-A mRNA in injured optic nerves. Chin J Fundus Dis 2003;19:247–249
Wang KC, Koprivica V, Kim JA, et al. Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth. Nature 2002;417:941–944
Liu BP, Fournier A, GrandPre T, et al. Myelin associated glycoprotein as a functional ligand for the Nogo-66 receptor. Science 2002;297:1190–1193
Brittis PA, Flanagan JG. Nogo domains and a Nogo receptor: implications for axon regeneration. Neuron 2001;30:11–14
Song XY, Zhong JH, Wang X, et al. Suppression of p75NTR does not promote regeneration of injured spinal cord in mice. J Neurosci 2004;24:542–546
Mi S, Lee X, Shao Z, et al. LINGO-1 is a component of the Nogo-66 receptor/p75 signaling complex. Nat Neurosci 2004;7:221–228
Hasegawa T, Ohno K, Sano M, et al. The differential expression patterns of messenger RNAs encoding Nogo-A and Nogo-receptor in the rat central nervous system. Brain Res Mol Brain Res 2005;133:119–130
Fournier AE, GrandPre T, Strittmatter SM. Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration. Nature 2001;409:341–346
McGee AW, Strittmatter SM. The Nogo-66 receptor: focusing myelin inhibition of axon regeneration. Trends Neurosci 2003;26:193–198
Fournier AE, Gould GC, Liu BP, et al. Truncated soluble Nogo receptor binds Nogo-66 and blocks inhibition of axon growth by myelin. J Neurosci 2002;22:8876–8883
Lehmann M, Fournier A, Selles-Navarro I, et al. Inactivation of Rho signaling pathway promotes CNS axon regeneration. J Neurosci 1999;19:7537–7547
Niederost B, Oertle T, Fritsche J, et al. Nogo-A and myelin-associated glycoprotein mediate neurite growth inhibition by antagonistic regulation of RhoA and Rac1. J Neurosci 2002;22:10368–10376
Fournier AE, Takizawa BT, Strittmatter SM. Rho kinase inhibition enhances axonal regeneration in the injured CNS. J Neurosci 2003;23:1416–1423
Wong ST, Henley JR, Kanning KC, et al. A p75(NTR) and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein. Nat Neurosci 2002;5:1302–1308
Wang X, Chun SJ, Treloar H, et al. Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact. J Neurosci 2002;22:5505–5515
Cai WQ. Neurobiology for Medicine, 1st edition. Chongqing: Southwest Normal University Press; 2001. p. 399
Acknowledgement
Foundation item: National Natural Science Foundation of China (No. 30572009).
Author information
Authors and Affiliations
Corresponding author
Additional information
Drs. Xiaolei, Jian, Chunlin, and Rongdi are from the Third Military Medical University, Department of Ophthalmology, Daping Hospital, Chongqing, China. E-mail: yinxiaolei971221@163.com
The authors have stated they do not have a significant financial interest or other relationship with any product manufacturer or provider of services discussed in this article. The authors also do not discuss the use of off-label products, which includes unlabeled, unapproved, or investigative products or devices.
We investigated Nogo receptor (NgR) expression in the retina of rats from postnatal day 0 to adulthood.
Rights and permissions
About this article
Cite this article
Xiaolei, Y., Chunlin, C., Rongdi, Y. et al. An Immunofluorescence–Histochemistry Study of the Nogo Receptor in the Rat Retina During Postnatal Development. Ann Ophthalmol 39, 140–144 (2007). https://doi.org/10.1007/s12009-007-0001-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12009-007-0001-1