IOVS Biophysical Journal
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


(Investigative Ophthalmology and Visual Science. 2004;45:2514-2521.)
© 2004 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.04-0065

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (18)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nour, M.
Right arrow Articles by Naash, M. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nour, M.
Right arrow Articles by Naash, M. I.

Modulating Expression of Peripherin/rds in Transgenic Mice: Critical Levels and the Effect of Overexpression

May Nour,1 Xi-Qin Ding,1 Heidi Stricker,1 Steven J. Fliesler,2,3 and Muna I. Naash1

1From the Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma; and the 2Departments of Ophthalmology and 3Pharmacological and Physiological Science, St. Louis University School of Medicine, St. Louis, Missouri.

PURPOSE. Mutations in the photoreceptor-specific protein peripherin/rds are associated with multiple retinal diseases. To date, attempts to achieve complete structural and functional rescue in animal models of peripherin/rds-induced retinal degeneration have not been successful. Gene therapy–directed approaches have been hindered by the haploinsufficiency phenotype, which dictates well-regulated expression of peripherin/rds protein levels.

METHODS.Using a transgenic mouse line expressing wild-type peripherin/rds (NMP), the authors evaluated the critical in vivo level of peripherin/rds needed to maintain photoreceptor structure and ERG function and assessed the consequences of peripherin/rds overexpression in both rods and cones by Western blot and immunoprecipitation analyses, immunohistochemistry, electron microscopy, and electroretinography. The NMP transgene included a C-terminal modification (P341Q) to facilitate detection of the transgenic protein in the presence of wild-type peripherin/rds, using the monoclonal antibody 3B6.

RESULTS.Peripherin/rds protein levels in NMP homozygotes were ~60% of wild-type levels. Western blot and immunoprecipitation analyses confirmed normal biochemical properties of the NMP protein when compared with wild-type peripherin/rds. Immunohistochemistry demonstrated appropriate localization of transgenic peripherin/rds protein to the disc rim region of photoreceptor outer segments. Total peripherin/rds levels in the retina were modulated by crossing NMP transgenic mice into different rds genetic backgrounds. A positive correlation was observed between peripherin/rds expression levels and the structural and functional integrity of photoreceptor outer segments. Overexpression of peripherin/rds caused no detectable adverse effects on rod or cone structure and function.

CONCLUSIONS.These findings may have significant implications regarding therapeutic intervention in peripherin/rds-associated retinal diseases.





This article has been cited by other articles:


Home page
Hum Mol GenetHome page
D. Chakraborty, X.-Q. Ding, S. M. Conley, S. J. Fliesler, and M. I. Naash
Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones
Hum. Mol. Genet., March 1, 2009; 18(5): 797 - 808.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
S. Conley, M. Nour, S. J. Fliesler, and M. I. Naash
Late-Onset Cone Photoreceptor Degeneration Induced by R172W Mutation in Rds and Partial Rescue by Gene Supplementation
Invest. Ophthalmol. Vis. Sci., December 1, 2007; 48(12): 5397 - 5407.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
A. F. X. Goldberg, L. M. Ritter, N. Khattree, N. S. Peachey, R. N. Fariss, L. Dang, M. Yu, and A. R. Bottrell
An Intramembrane Glutamic Acid Governs Peripherin/rds Function for Photoreceptor Disk Morphogenesis
Invest. Ophthalmol. Vis. Sci., July 1, 2007; 48(7): 2975 - 2986.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
R. Farjo, J. S. Skaggs, B. A. Nagel, A. B. Quiambao, Z. A. Nash, S. J. Fliesler, and M. I. Naash
Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors
J. Cell Biol., April 10, 2006; 173(1): 59 - 68.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the Association for Research in Vision and Ophthalmology