April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Myofibroblasts Are The Main Contracting Cellular Elements At The Border Of Stage III And IV Macular Holes
Author Affiliations & Notes
  • Constantin J. Pournaras
    Vitreo-retinal Unit, Ophthalmology,
    Geneva University Hospitals, Geneva, Switzerland
  • Marie-Luce Bochaton-Piallat
    Department of Pathology and Immunology,
    Geneva University Hospitals, Geneva, Switzerland
  • Nicole Gilodi
    Department of Ophthalmology,
    Geneva University Hospitals, Geneva, Switzerland
  • Miltiadis K. Tsilimbaris
    Vitreo-retinal Unit, Ophthalmology,
    Geneva University Hospitals, Geneva, Switzerland
  • Efstratios Mendrinos
    Vitreo-retinal Unit, Ophthalmology,
    Geneva University Hospitals, Geneva, Switzerland
  • Footnotes
    Commercial Relationships  Constantin J. Pournaras, None; Marie-Luce Bochaton-Piallat, None; Nicole Gilodi, None; Miltiadis K. Tsilimbaris, None; Efstratios Mendrinos, None
  • Footnotes
    Support  FN 320000-122190
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 4489. doi:
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      Constantin J. Pournaras, Marie-Luce Bochaton-Piallat, Nicole Gilodi, Miltiadis K. Tsilimbaris, Efstratios Mendrinos; Myofibroblasts Are The Main Contracting Cellular Elements At The Border Of Stage III And IV Macular Holes . Invest. Ophthalmol. Vis. Sci. 2011;52(14):4489.

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Abstract

Purpose: : Myofibroblasts play a major role in the production of retractile phenomena causing contraction or shrinkage of the epiretinal membranes (ERM) in proliferative vitreoretinopathy, diabetic retinopathy or idiopathic macular epiretinal membranes. The presence of a-smooth muscle actin (a-SMA)-positive myofibroblasts and of ED-A fibronectin (FN), one of the main inducers of myofibroblastic differentiation was studied in internal limiting membranes (ILM) removed during macular hole surgery.

Methods: : Samples of ILMs following macular hole surgery in 9 eyes were collected. Double immunofluorescence staining with antibodies recognizing a-SMA and ED-A FN followed by confocal microscopy analysis as well as electronic microscopy were performed.

Results: : a-SMA and ED-A FN were detected in ILM removed in stage III and IV macular holes. ED-A FN was expressed in close relation with a-SMA-positive myofibroblasts predominately located close to the border of the macular hole area. Distally to the hole area the ILM specimens were a-SMA and ED-A FN negative. No a-SMA staining was observed in ILM specimens of stage II macular hole specimens.

Conclusions: : Scanning electron microscopy indicated that cellular migration was not apparent around the macular hole in the early stage of the development of this pathology.Cellular elements expressing contractile properties related to a-SMA, typical of myofibroblasts differentiation, appear to be present at late stage macular holes.

Keywords: retina • macular holes 
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