HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Human cone photoreceptor dependence on RPE65 isomerase.

Abstract
The visual (retinoid) cycle, the enzymatic pathway that regenerates chromophore after light absorption, is located primarily in the retinal pigment epithelium (RPE) and is essential for rod photoreceptor survival. Whether this pathway also is essential for cone photoreceptor survival is unknown, and there are no data from man or monkey to address this question. The visual cycle is naturally disrupted in humans with Leber congenital amaurosis (LCA), which is caused by mutations in RPE65, the gene that encodes the retinoid isomerase. We investigated such patients over a wide age range (3-52 years) for effects on the cone-rich human fovea. In vivo microscopy of the fovea showed that, even at the youngest ages, patients with RPE65-LCA exhibited cone photoreceptor loss. This loss was incomplete, however, and residual cone photoreceptor structure and function persisted for decades. Basic questions about localization of RPE65 and isomerase activity in the primate eye were addressed by examining normal macaque. RPE65 was definitively localized by immunocytochemistry to the central RPE and, by immunoblotting, appeared to concentrate in the central retina. The central retinal RPE layer also showed a 4-fold higher retinoid isomerase activity than more peripheral RPE. Early cone photoreceptor losses in RPE65-LCA suggest that robust RPE65-based visual chromophore production is important for cones; the residual retained cone structure and function support the speculation that alternative pathways are critical for cone photoreceptor survival.
AuthorsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, Elise Heon, Marcin Golczak, William A Beltran, Alexander Sumaroka, Sharon B Schwartz, Alejandro J Roman, Elizabeth A M Windsor, James M Wilson, Gustavo D Aguirre, Edwin M Stone, Krzysztof Palczewski
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 104 Issue 38 Pg. 15123-8 (Sep 18 2007) ISSN: 0027-8424 [Print] United States
PMID17848510 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Carrier Proteins
  • Eye Proteins
  • retinoid isomerohydrolase
  • cis-trans-Isomerases
Topics
  • Adolescent
  • Adult
  • Animals
  • Carrier Proteins (analysis, genetics, metabolism)
  • Child
  • Child, Preschool
  • Eye Proteins (analysis, genetics, metabolism)
  • Female
  • Fluorescent Antibody Technique
  • Humans
  • Macaca fascicularis
  • Male
  • Middle Aged
  • Optic Atrophy, Hereditary, Leber (metabolism)
  • Pigment Epithelium of Eye (enzymology, metabolism)
  • Retinal Cone Photoreceptor Cells (physiology)
  • cis-trans-Isomerases (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: