Aberrant glycosylation in the human trabecular meshwork

Proteomics Clin Appl. 2014 Apr;8(3-4):130-42. doi: 10.1002/prca.201300031. Epub 2014 Mar 7.

Abstract

Purpose: To determine the difference in protein glycosylation and glycosylation enzyme levels between glaucomatous and control trabecular meshwork (TM).

Experimental design: Glaucomatous and normal donor (n = 12 each) TM tissues, lectin fluorescence, fluorophore-assisted carbohydrate analyses, and quantitative MS were used to determine the glycosylation levels. Primary TM cells and glycosylation inhibitors were used to determine their effect on cell shape and motility.

Results: In contrast to elevated levels of glycoproteins determined by lectin fluorescence, simultaneous hyper- and hypo-glycosylation in glaucomatous TM was revealed by fluorophore-assisted carbohydrate analyses. Analyses of enzymes showed elevation of beta-glycosidase 1 and decrease in galactosyltransferase family 6 domain containing protein 1 in the glaucomatous TM. Quantitative MS identified select protein level changes between glaucomatous and normal TM. Primary TM cells were treated with inhibitors to elicit hypo-glycosylation, which affected cell shape, motility, and fluorescent tracer transport across a layer of TM cells.

Conclusions and clinical relevance: Global protein glycosylation is aberrant in glaucomatous TM compared to controls. The results presented here suggest that the alteration in global TM protein glycosylation encompassing cellular and extracellular matrix proteins contributes to glaucoma pathology likely mediated through changes in properties of TM cells.

Keywords: Carbohydrate electrophoresis; Glaucoma; Glycosylation; Trabecular meshwork.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Enzymes / biosynthesis*
  • Extracellular Matrix Proteins / biosynthesis*
  • Gene Expression Regulation, Enzymologic
  • Glaucoma / genetics*
  • Glaucoma / pathology
  • Glycosylation
  • Humans
  • Trabecular Meshwork / enzymology
  • Trabecular Meshwork / metabolism*
  • Trabecular Meshwork / pathology

Substances

  • Enzymes
  • Extracellular Matrix Proteins