Alterations in the aqueous humor proteome in patients with Fuchs endothelial corneal dystrophy

Matthew R. Richardson, Zaneer M. Segu, Marianne O. Price, Xianyin Lai, Frank Witzmann, Yehia Mechref, Mervin Yoder, Francis W. Price

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Fuchs endothelial corneal dystrophy (FECD) is a progressive disorder characterized by corneal endothelial decompensation leading to corneal edema, clouding, and vision impairment. Despite improved understanding over the last century since its first description, the exact mechanism(s) behind the pathogenesis of FECD remain unknown, and surgical correction is the only effective treatment available. Previous studies have suggested a role for changes in aqueous humor (AH) composition in FECD pathogenesis, so to explore this possibility, we probed the AH proteome for alterations correlating with end-stage corneal disease. Following albumin depletion we performed label-free quantitative tandem mass spectrometry on proteins isolated from patients with and without FECD who were scheduled to undergo routine cataract extraction. We identified 64 proteins, most of which were identified in previous AH proteomic studies of patients with cataracts, in the albumin-depleted fraction. The levels of five of these were significantly lower (afamin, complement C3, histidine-rich glycoprotein, immunoglobulin heavy [IgH], and protein family with sequence similarity 3, member C [FAM3C]), while the levels of one (suprabasin) was significantly higher in patients with FECD compared to controls (p≤0.01). We also identified 34 proteins in the albumin-bound fraction, four of which were significantly elevated in patients with FECD including a hemoglobin fragment, immunoglobulin kappa (IgK), immunoglobulin lambda (IgL), and uncharacterized protein albumin (ALB), (p≤0.01). Although it has been reported that females have a greater extent of disease than males, we were unable to detect any significant differences in protein levels due to gender. Because FECD is a progressive disorder, regression analyses were performed to determine any significant correlations with age, and of interest retinol-binding protein 3 was significantly correlated with age in patients with FECD (p≤0.01), whereas no proteins in the control group correlated with age. This is the first report indicating alterations in the AH proteome with FECD, and taken together this study suggests several novel hypotheses regarding AH proteins role in FECD pathogenesis.

Original languageEnglish
Pages (from-to)2376-2383
Number of pages8
JournalMolecular Vision
Volume16
StatePublished - 2010

Fingerprint

Fuchs' Endothelial Dystrophy
Aqueous Humor
Proteome
Albumins
Proteins
Immunoglobulins
Corneal Diseases
Corneal Edema
Retinol-Binding Proteins
Immunoglobulin Fragments
Complement C3
Cataract Extraction
Tandem Mass Spectrometry
Proteomics
Cataract
Hemoglobins

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Richardson, M. R., Segu, Z. M., Price, M. O., Lai, X., Witzmann, F., Mechref, Y., ... Price, F. W. (2010). Alterations in the aqueous humor proteome in patients with Fuchs endothelial corneal dystrophy. Molecular Vision, 16, 2376-2383.

Alterations in the aqueous humor proteome in patients with Fuchs endothelial corneal dystrophy. / Richardson, Matthew R.; Segu, Zaneer M.; Price, Marianne O.; Lai, Xianyin; Witzmann, Frank; Mechref, Yehia; Yoder, Mervin; Price, Francis W.

In: Molecular Vision, Vol. 16, 2010, p. 2376-2383.

Research output: Contribution to journalArticle

Richardson, MR, Segu, ZM, Price, MO, Lai, X, Witzmann, F, Mechref, Y, Yoder, M & Price, FW 2010, 'Alterations in the aqueous humor proteome in patients with Fuchs endothelial corneal dystrophy', Molecular Vision, vol. 16, pp. 2376-2383.
Richardson, Matthew R. ; Segu, Zaneer M. ; Price, Marianne O. ; Lai, Xianyin ; Witzmann, Frank ; Mechref, Yehia ; Yoder, Mervin ; Price, Francis W. / Alterations in the aqueous humor proteome in patients with Fuchs endothelial corneal dystrophy. In: Molecular Vision. 2010 ; Vol. 16. pp. 2376-2383.
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