The expression of advanced glycation endproduct receptors in rpe cells associated with basal deposits in human maculas

Yuko Yamada, Kazuko Ishibashi, Kazuki Ishibashi, Imran A. Bhutto, Jane Tian, Gerard Anthony Lutty, James Handa

Research output: Contribution to journalArticle

Abstract

Basal deposits within Bruch's membrane are associated with aging and age-related macular degeneration (AMD) although the factors causing their formation are incompletely understood. Advanced glycation endproducts (AGEs) accumulate in Bruch's membrane including basal deposits and drusen with aging. One mechanism by which AGEs alter a cell's phenotype is via AGE receptors. The purpose of this study was to immunolocalize and quantify the expression of AGE receptors by RPE cells associated with basal deposits or normal Bruch's membrane that were microdissected from human maculas. Postmortem eyes from 14 aged control donors and five donors with non-neovascular AMD were cryopreserved. RPE cells associated with normal Bruch's membrane or basal deposits were laser capture microdissected. The RNA was extracted and used for RT-qPCR to quantify the expression of RAGE, AGE R1, AGE R2, and AGE R3. Streptavidin alkaline phosphatase immunohistochemistry for these receptors was also performed and sections were bleached from 14 normal and nine AMD donors. RT-qPCR showed significant upregulation of RAGE, AGE R1, and AGE R3 in RPE cells overlying basal deposits compared to cells attached to morphologically normal Bruch's membrane. Immunohistochemical analysis for RAGE, AGER1, R2, and R3 showed diffuse, light staining of RPE cells and strong choriocapillaris staining in areas of normal Bruch's membrane. In areas of basal deposits, the RPE had more intense staining for RAGE and AGER1 compared to regions of normal Bruch's membrane. These results suggest that AGE receptors could influence the formation of basal deposits during aging and AMD.

Original languageEnglish (US)
Pages (from-to)840-848
Number of pages9
JournalExperimental Eye Research
Volume82
Issue number5
DOIs
StatePublished - May 2006

Fingerprint

Bruch Membrane
Macular Degeneration
Staining and Labeling
Streptavidin
Advanced Glycosylation End Product-Specific Receptor
Alkaline Phosphatase
Lasers
Up-Regulation
Immunohistochemistry
RNA
Phenotype
Light

Keywords

  • Advanced glycation endproduct receptor complex
  • Advanced glycation endproducts
  • Age-related macular degeneration
  • Aging
  • Basal deposits
  • Bruch's membrane
  • Receptor for advanced glycation endproducts
  • Retinal pigment epithelium

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems

Cite this

The expression of advanced glycation endproduct receptors in rpe cells associated with basal deposits in human maculas. / Yamada, Yuko; Ishibashi, Kazuko; Ishibashi, Kazuki; Bhutto, Imran A.; Tian, Jane; Lutty, Gerard Anthony; Handa, James.

In: Experimental Eye Research, Vol. 82, No. 5, 05.2006, p. 840-848.

Research output: Contribution to journalArticle

Yamada, Yuko ; Ishibashi, Kazuko ; Ishibashi, Kazuki ; Bhutto, Imran A. ; Tian, Jane ; Lutty, Gerard Anthony ; Handa, James. / The expression of advanced glycation endproduct receptors in rpe cells associated with basal deposits in human maculas. In: Experimental Eye Research. 2006 ; Vol. 82, No. 5. pp. 840-848.
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abstract = "Basal deposits within Bruch's membrane are associated with aging and age-related macular degeneration (AMD) although the factors causing their formation are incompletely understood. Advanced glycation endproducts (AGEs) accumulate in Bruch's membrane including basal deposits and drusen with aging. One mechanism by which AGEs alter a cell's phenotype is via AGE receptors. The purpose of this study was to immunolocalize and quantify the expression of AGE receptors by RPE cells associated with basal deposits or normal Bruch's membrane that were microdissected from human maculas. Postmortem eyes from 14 aged control donors and five donors with non-neovascular AMD were cryopreserved. RPE cells associated with normal Bruch's membrane or basal deposits were laser capture microdissected. The RNA was extracted and used for RT-qPCR to quantify the expression of RAGE, AGE R1, AGE R2, and AGE R3. Streptavidin alkaline phosphatase immunohistochemistry for these receptors was also performed and sections were bleached from 14 normal and nine AMD donors. RT-qPCR showed significant upregulation of RAGE, AGE R1, and AGE R3 in RPE cells overlying basal deposits compared to cells attached to morphologically normal Bruch's membrane. Immunohistochemical analysis for RAGE, AGER1, R2, and R3 showed diffuse, light staining of RPE cells and strong choriocapillaris staining in areas of normal Bruch's membrane. In areas of basal deposits, the RPE had more intense staining for RAGE and AGER1 compared to regions of normal Bruch's membrane. These results suggest that AGE receptors could influence the formation of basal deposits during aging and AMD.",
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