QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

HOME  |   SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, December 27, 2006, 26(52):13523-13530; doi:10.1523/JNEUROSCI.4021-06.2006

This Article Full Text Full Text (PDF) Submit an eLetter Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (18) Citing Articles via Google Scholar Google Scholar Articles by Wen, R. Articles by Sieving, P. A. Search for Related Content PubMed PubMed Citation Articles by Wen, R. Articles by Sieving, P. A. Pubmed/NCBI databases Gene GEO Profiles HomoloGene UniGene Substance via MeSH

 Previous Article  |  Next Article 

Cellular/Molecular
Regulation of Rod Phototransduction Machinery by Ciliary Neurotrophic Factor

Rong Wen,¹ Ying Song,¹ Sten Kjellstrom,² Atsuhiro Tanikawa,² Yun Liu,¹ Yiwen Li,¹ Lian Zhao,¹ Ronald A. Bush,² Alan M. Laties,¹ and Paul A. Sieving^2,3

¹Departments of Ophthalmology, University of Pennsylvania, School of Medicine, Philadelphia, Pennsylvania 19104, ²National Institute on Deafness and Other Communication Disorders, and ³National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892

Correspondence should be addressed to Dr. Rong Wen, Department of Ophthalmology, D-603 Richards Building, University of Pennsylvania, School of Medicine, Philadelphia, PA 19104. Email: rwen{at}mail.med.upenn.edu

Ciliary neurotrophic factor (CNTF) promotes photoreceptor survival but also suppresses electroretinogram (ERG) responses. This has caused concerns about whether CNTF is detrimental to the function of photoreceptors because it is considered to be a potential treatment for retinal degenerative disorders. Here we report that the suppression of ERG responses is attributable to negative regulation of the phototransduction machinery in rod photoreceptors. Intravitreal injection of recombinant human CNTF protein in rat results in a series of biochemical and morphological changes in rod photoreceptors. CNTF induces a decrease in rhodopsin expression and an increase in arrestin level. Morphologically, CNTF treatment causes a shortening of rod outer segments (ROS). All of these changes are fully reversible. The lower rhodopsin level and shortened ROS reduce the photon catch of rods. Less rhodopsin and more arrestin dramatically increase the arrestin-to-rhodopsin ratio so that more arrestin molecules are available to quench the photoexcited rhodopsin. The overall effect of CNTF is to negatively regulate the phototransduction machinery, which reduces the photoresponsiveness of rods, resulting in lower ERG amplitude at a given intensity of light stimulus. The CNTF-induced changes in rods are similar to those in light-induced photoreceptor plasticity. Whether CNTF-induced changes in rods are through the same mechanism that mediates light-induced photoreceptor plasticity remains to be answered.

Key words: CNTF; phototransduction; Müller cells; ERG; electroretinogram; retina; rod

---

Received Sept. 14, 2006; revised Nov. 23, 2006; accepted Nov. 25, 2006.

Correspondence should be addressed to Dr. Rong Wen, Department of Ophthalmology, D-603 Richards Building, University of Pennsylvania, School of Medicine, Philadelphia, PA 19104. Email: rwen{at}mail.med.upenn.edu

This article has been cited by other articles:

				S.-W. M. Koh, J. Celeste, and C. Y. P. Ku Functional CNTF Receptor {alpha} Subunit Restored by Its Recombinant in Corneal Endothelial Cells in Stored Human Donor Corneas: Connexin-43 Upregulation Invest. Ophthalmol. Vis. Sci., April 1, 2009; 50(4): 1801 - 1807. [Abstract] [Full Text] [PDF]

				M. Sasaki, Y. Ozawa, T. Kurihara, K. Noda, Y. Imamura, S. Kobayashi, S. Ishida, and K. Tsubota Neuroprotective Effect of an Antioxidant, Lutein, during Retinal Inflammation Invest. Ophthalmol. Vis. Sci., March 1, 2009; 50(3): 1433 - 1439. [Abstract] [Full Text] [PDF]

				Y. Ozawa, K. Nakao, T. Kurihara, T. Shimazaki, S. Shimmura, S. Ishida, A. Yoshimura, K. Tsubota, and H. Okano Roles of STAT3/SOCS3 Pathway in Regulating the Visual Function and Ubiquitin-Proteasome-dependent Degradation of Rhodopsin during Retinal Inflammation J. Biol. Chem., September 5, 2008; 283(36): 24561 - 24570. [Abstract] [Full Text] [PDF]

				T. J. McGill, G. T. Prusky, R. M. Douglas, D. Yasumura, M. T. Matthes, G. Nune, K. Donohue-Rolfe, H. Yang, D. Niculescu, W. W. Hauswirth, et al. Intraocular CNTF Reduces Vision in Normal Rats in a Dose-Dependent Manner Invest. Ophthalmol. Vis. Sci., December 1, 2007; 48(12): 5756 - 5766. [Abstract] [Full Text] [PDF]

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help