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

REFERENCES

• Kawahara S, Hata Y, Kita T et al. Potent inhibition of cicatricial contraction in proliferative vitreoretinal diseases by statins. Diabetes. 2008;57:2784–2793.
   PubMed Web of Science ®Google Scholar
• Cardillo JA, Farah ME, Mitre J et al. An intravitreal biodegradable sustained release naproxen and 5-fluorouracil system for the treatment of experimental post-traumatic proliferative vitreoretinopathy. Br J Ophthalmol. 2004;88:1201–1205.
   PubMed Web of Science ®Google Scholar
• Andrews A, Balciunaite E, Leong FL et al. Platelet-derived growth factor plays a key role in proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci. 1999;40:2683–2689.
   PubMed Web of Science ®Google Scholar
• Shevchenko A, Wilm M, Vorm O, Mann M. Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels. Anal Chem. 1996;68:850–858.
   PubMed Web of Science ®Google Scholar
• Machemer R, Aaberg TM, Freeman HM, Irvine AR, Lean JS, Michels RM. An updated classification of retinal detachment with proliferative vitreoretinopathy. Am J Ophthalmol. 1991;112:159–165.
   PubMed Web of Science ®Google Scholar
• Zhu K, Zhao J, Lubman DM, Miller FR, Barder TJ. Protein pI shifts due to posttranslational modifications in the separation and characterization of proteins. Anal Chem. 2005;77:2745–2755.
   Google Scholar
• Kantorow M, Piatigorsky J. Phosphorylations of alpha A- and alpha B-crystallin. Int J Biol Macromol. 1998;22:307–314.
   PubMed Web of Science ®Google Scholar
• Glaser BM, Cardin A, Biscoe B. Proliferative vitreoretinopathy. The mechanism of development of vitreoretinal traction. Ophthalmology. 1987;94:327–332.
   PubMed Web of Science ®Google Scholar
• Wiedemann P, Weller M, Heimann K. [Proliferative vitreoretinopathy: new discoveries in pathophysiology and therapy]. Klin Monbl Augenheilkd. 1990;197:355–361.
   Google Scholar
• Chrzanowska-Wodnicka M, Burridge K. Rho-stimulated contractility drives the formation of stress fibers and focal adhesions. J Cell Biol. 1996;133:1403–1415.
   PubMed Web of Science ®Google Scholar
• Wilkinson S, Paterson HF, Marshall CJ. Cdc42-MRCK and Rho-ROCK signalling cooperate in myosin phosphorylation and cell invasion. Nat Cell Biol. 2005;7:255–261.
   PubMed Web of Science ®Google Scholar
• Giannone G, Dubin-Thaler BJ, Rossier O et al. Lamellipodial actin mechanically links myosin activity with adhesion-site formation. Cell. 2007;128:561–575.
   PubMed Web of Science ®Google Scholar
• Romer LH, Birukov KG, Garcia JG. Focal adhesions: paradigm for a signaling nexus. Circ Res. 2006;98:606–616.
   PubMed Web of Science ®Google Scholar
• Connell LE, Helfman DM. Myosin light chain kinase plays a role in the regulation of epithelial cell survival. J Cell Sci. 2006;119:2269–2281.
   Google Scholar
• Weller M, Wiedemann P, Heimann K. Proliferative vitreoretinopathy–is it anything more than wound healing at the wrong place? Int Ophthalmol. 1990;14:105–117.
   PubMed Web of Science ®Google Scholar
• Witte MB, Barbul A, Schick MA, Vogt N, Becker HD. Upregulation of arginase expression in wound-derived fibroblasts. J Surg Res. 2002;105:35–42.
   Google Scholar
• Yu J, Liu F, Cui SJ et al. Vitreous proteomic analysis of proliferative vitreoretinopathy. Proteomics. 2008;8:3667–3678.
   PubMed Web of Science ®Google Scholar
• Sly WS, Hu PY. Human carbonic anhydrases and carbonic anhydrase deficiencies. Annu Rev Biochem. 1995;64:375–401.
   PubMed Web of Science ®Google Scholar
• Moor AN, Fliegel L. Protein kinase-mediated regulation of the Na(+)/H(+) exchanger in the rat myocardium by mitogen-activated protein kinase-dependent pathways. J Biol Chem. 1999;274:22985–22992.
   PubMed Web of Science ®Google Scholar
• Grisanti S, Wiedemann P, Weller M, Heimann K, Zilles K. The significance of complement in proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci. 1991;32:2711–2717.
   Google Scholar
• Baudouin C, Fredj-Reygrobellet D, Gordon WC et al. Immunohistologic study of epiretinal membranes in proliferative vitreoretinopathy. Am J Ophthalmol. 1990;110:593–598.
   PubMed Web of Science ®Google Scholar
• Weller M, Heimann K, Wiedemann P. The pathogenesis of vitreoretinal proliferation and traction: a working hypothesis. Med Hypotheses. 1990;31:157–159.
   PubMed Web of Science ®Google Scholar
• Stafford JL, Belosevic M. Transferrin and the innate immune response of fish: identification of a novel mechanism of macrophage activation. Dev Comp Immunol. 2003;27:539–554.
   PubMed Web of Science ®Google Scholar
• Charteris DG, Hiscott P, Grierson I, Lightman SL. Proliferative vitreoretinopathy. Lymphocytes in epiretinal membranes. Ophthalmology. 1992;99:1364–1367.
   PubMed Web of Science ®Google Scholar
• Böker T, Augustin AJ, Breipohl W, Spitznas M, Lutz J. Increased lipid peroxide level and myeloperoxidase activity in the vitreous of patients suffering from proliferative vitreoretinopathy. Graefes Arch Clin Exp Ophthalmol. 1994;232:652–656.
   PubMed Web of Science ®Google Scholar
• Sax CM, Piatigorsky J. Expression of the alpha-crystallin/small heat-shock protein/molecular chaperone genes in the lens and other tissues. Adv Enzymol Relat Areas Mol Biol. 1994;69:155–201.
   PubMedGoogle Scholar
• Robinson ML, Overbeek PA. Differential expression of alpha A- and alpha B-crystallin during murine ocular development. Invest Ophthalmol Vis Sci. 1996;37:2276–2284.
   PubMedGoogle Scholar
• Klemenz R, Fröhli E, Steiger RH, Schäfer R, Aoyama A. Alpha B-crystallin is a small heat shock protein. Proc Natl Acad Sci USA. 1991;88:3652–3656.
   PubMed Web of Science ®Google Scholar
• Kase S, Parikh JG, Rao NA. Expression of alpha-crystallin in retinoblastoma. Arch Ophthalmol. 2009;127:187–192.
   Google Scholar
• Francke M, Faude F, Pannicke T et al. Electrophysiology of rabbit Müller (glial) cells in experimental retinal detachment and PVR. Invest Ophthalmol Vis Sci. 2001;42:1072–1079.
   Google Scholar
• Laqua H, Machemer R. Glial cell proliferation in retinal detachment (massive periretinal proliferation). Am J Ophthalmol. 1975;80:602–618.
   PubMed Web of Science ®Google Scholar
• Newman EA. Voltage-dependent calcium and potassium channels in retinal glial cells. Nature. 1985;317:809–811.
   Google Scholar
• Pan SJ, Zhu M, Raizada MK, Sumners C, Gelband CH. ANG II-mediated inhibition of neuronal delayed rectifier K+ current: role of protein kinase C-alpha. Am J Physiol, Cell Physiol. 2001;281:C17–C23.
   Google Scholar
• Shimoda LA, Sylvester JT, Sham JS. Inhibition of voltage-gated K+ current in rat intrapulmonary arterial myocytes by endothelin-1. Am J Physiol. 1998;274:L842–L853.
   PubMed Web of Science ®Google Scholar
• Peretz T, Levin G, Moran O, Thornhill WB, Chikvashvili D, Lotan I. Modulation by protein kinase C activation of rat brain delayed-rectifier K+ channel expressed in Xenopus oocytes. FEBS Lett. 1996;381:71–76.
   Google Scholar
• Holmes TC, Fadool DA, Levitan IB. Tyrosine phosphorylation of the Kv1.3 potassium channel. J Neurosci. 1996;16:1581–1590.
   PubMed Web of Science ®Google Scholar