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Vol. 40, No. 3-4, 2008   

Free Abstract     Article (References)     Article (PDF 444 KB)     

Paper

Ccl2/Cx3cr1-Deficient Mice: An Animal Model for Age-Related Macular Degeneration
Chi-Chao Chana, Robert J. Rossa, Defen Shena, Xiaoyan Dinga, Zigurts Majumdarb, Christine M. Bojanowskia, Min Zhoua, Norman Salem, Jr.c, Robert Bonnerb, Jingsheng Tuoa

aSection of Immunopathology, Laboratory of Immunology, National Eye Institute,
bSection on Medical Biophysics, Laboratory of Integrative and Medical Biophysics, National Institute of Child Health and Human Development, and
cLaboratory of Membrane Biochemistry and Biophysics, National Institute of Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Md., USA

Address of Corresponding Author

Ophthalmic Res 2008;40:124-128 (DOI: 10.1159/000119862)


 goto top of page Key Words

  • Age-related macular degeneration
  • Animal model
  • CCL2
  • CX3CR1
  • Retinal pigment epithelium
  • N-retinylidene-N-retinylethanolamine
  • Chaperone
  • Omega-3 long-chain polyunsaturated fatty acids

 goto top of page Abstract

Background/Aims: Senescent Ccl2-/- mice develop cardinal features of human age-related macular degeneration (AMD). Loss-of-function single-nucleotide polymorphisms within CX3CR1 are associated with AMD. Methods: We generated Ccl2-/-/Cx3cr1-/- [double-knockout (DKO)] mice and evaluated the eyes using fundoscopy routine histology, immunochemistry, biochemistry and proteomics. Results: At 6 weeks old, all DKO mice developed AMD-like retinal lesions such as abnormal retinal pigment epithelium cells, drusen, photoreceptor atrophy and choroidal neovascularization, which progressed with age and reversed with high omega-3 long-chain polyunsaturated fatty acid diet. N-retinylidene-N-retinylethanolamine (A2E), a major lipofuscin fluorophore, illustrated by an emission peak at ~600 nm, was significantly higher in DKO retinal pigment epithelium. Decreased ERp29 was found in the retina of DKO mice. Conclusion: A broad spectrum of AMD pathologies with early onset and high penetrance in these mice implicate certain chemokines, A2E and endoplasmic reticulum proteins in AMD pathogenesis.

Copyright © 2008 S. Karger AG, Basel


 goto top of page Author Contacts

Chi-Chao Chan, MD
Building 10, Room 10N103
10 Center Drive, NIH/NEI
Bethesda, MD 20892-1857 (USA)
Tel. +1 301 496 0417, Fax +1 301 402 8664, E-Mail chanc@nei.nih.gov


 goto top of page Article Information

Published online: April 18, 2008
Number of Print Pages : 5
Number of Figures : 5, Number of Tables : 0, Number of References : 24

 
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Medline Abstract (ID 18421225)
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copyright  © 2009 S. Karger AG, Basel