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Original Article

Proteomics of Post-Traumatic Proliferative Vitreoretinopathy in Rabbit Retina Reveals Alterations to a Variety of Functional Proteins

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Pages 318-326 | Received 26 Mar 2011, Accepted 12 Oct 2011, Published online: 01 Feb 2012
 

Abstract

Purpose: The purpose of this study was to investigate the protein profiles and pathogenesis in rabbit retinas from normal and post-traumatic proliferative vitreoretinopathy (PVR).

Materials and methods: A modified rabbit model of post-traumatic PVR was modified used in the study. Two-dimensional gel electrophoresis (2-DE) coupled with mass spectrometry (MS) were utilized to identify the changes to the protein profiles of rabbit retina. The myosin light chains-2 (MLC2) was subsequently chosen as a target for its biggest difference in 2-DE gels using Western blot, immunohistochemistry and MTT assay.

Results: Comparative gel analysis revealed that 20 spots were up-regulated or novel emerged and 12 were down-regulated or even disappeared in PVR retinas. The majority of changes could consist of the following functional groups of proteins including the cell skeleton proteins; the wound healing/cell adhesion proteins; the proteins involved in metabolism and in blood-retina barrier destruction; oxidative stress-related proteins and the ion channel proteins. Western blot analysis confirmed that MLC2 protein expression was upregulated in PVR retinas. MTT assay showed that the anti-MLC2 monoclonal antibody significantly decreased the proliferation in ARPE-19 cells stimulated with different concentrations and times in vitro experiment.

Conclusions: Our results suggested that PVR is a complicated pathology process with alterations in expression of a variety of functional proteins rather than a single key protein. The data reported may be useful for further studies on pathogenesis of human PVR and for the screening of biomarkers to develop new potential therapeutic approaches.

Declaration of interest: This work was supported by Project of Health Bureau Foundation of Chongqing (2008-2-36) and Project of Medical Science Foundation of the First Affiliated Hospital of Chongqing Medical University (YXJJ2009-10).

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