J Korean Ophthalmol Soc.  2012 Oct;53(10):1512-1522.

Human Vitreous Proteomes in Idiopathic Macular Hole

Affiliations
  • 1Happyeye21 Clinic, Gwangju, Korea.
  • 2Samsung Eye & ENT Clinic Center, Jeonju, Korea. Opth20@freechal.com

Abstract

PURPOSE
To investigate the vitreous proteomic profiles of macular hole (MH) patients compared to donor eyes and epiretinal membrane (ERM) patients.
METHODS
Ten donor eyes, 25 MH patients (15 MH without posterior vitreous detachment (PVD) and 10 MH with PVD), 10 ERM patients and 4 patients with vitreomacular traction syndrome (VMTS) were enrolled in the present study. The undiluted vitreous samples were obtained from all eyes. Proteins were identified using the micro-RPLC/MS/MS technique and using mass spectrometric data analysis from the IPI database. Proteins were searched for the function, subcellular location and tissue specificity using the Uniprot database.
RESULTS
The mean vitreous protein concentrations were the highest (p < 0.01) in MH patients without PVD. There were no qualitative changes according to the age of donor eyes. However, the authors newly-identified 12 proteins (i.e. vasorin) in donor eyes. Ten out of 136 proteins (7.3%) (i.e. retinoschisin) were exclusively detected in the MH samples. S100A8 was exclusively detected in eyes without PVD, whereas CD59 was exclusively detected in eyes with PVD.
CONCLUSIONS
The results suggest there is a small difference in the vitreous proteomic profiles in MH patients compared to donor eyes or ERM patients, and that the expression of vitreous proteins is closely associated with the presence of PVD.

Keyword

Macular hole; Posterior vitreous detachment; Proteomics; S100; Vitreous

MeSH Terms

Epiretinal Membrane
Eye
Humans
Organ Specificity
Proteins
Proteome
Proteomics
Retinal Perforations
Statistics as Topic
Tissue Donors
Traction
Vitreous Detachment
Proteins
Proteome

Figure

  • Figure 1 Classification of patients based on the features of optical coherence tomography (OCT). VMTS = vitreomacular traction syndrome; MH = macular hole; PVD = posterior vitreous detachment; ERM = epiretinal membrane.

  • Figure 2 Comparison of vitreous proteomes among donor eyes, macular hole (MH) samples and epiretinal membrane (ERM) samples. (A) Average protein concentrations in vitreous. (B) Venn diagram of proteins identified from the control (donor eye), MH and ERM samples. (C) Function categorizations of vitreous proteins identified.

  • Figure 3 Comparison of vitreous proteomes according to the presence of posterior vitreous detachment (PVD). (A) Average protein concentrations in vitreous. (B) Venn diagram of proteins identified based on the status of PVD. (C) Function categorizations of vitreous proteins identified.

  • Figure 4 Representative MS/MS spectrum from four proteins that was identified specific for macular hole and epiretinal membrane.


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