Literature DB >> 9820791

Proteoglycan distribution during healing of corneal stromal wounds in chick.

N Sundarraj1, D Fite, R Belak, S Sundarraj, J Rada, S Okamoto, J Hassell.   

Abstract

Proteoglycan distribution during corneal stromal healing in growing corneas of young chicks were histologically and immunohistochemically analysed. Single linear incisions to produce partial-thickness wounds were made in the corneas of 5 day old chicks. The corneas were harvested at different times after wounding and processed for either histochemical analyses using periodic acid-Schiff's reaction (PAS) or for indirect immunofluorescence analyses of lumican, keratocan, keratan sulfate, perlecan and laminin. Linear corneal stromal incisions were completely covered by migrated stratified epithelium by day 2 post wounding and resulted in a gaping wound with a thinner stroma. New stromal scar tissue formed between the epithelium and the original stroma that resulted in partial restoration of stromal thickness. During the first two to three weeks of healing, the stromal tissue filling the depression formed from the gaping wound, was hypercellular and PAS positive, indicating significantly higher levels of glycoprotein content but no new Bowman's membrane was formed. By four weeks, the scar tissue occupied a 2-3 mm wide region. Immunofluorescence analyses indicated that other major differences in the healing and normally growing stroma were the increased synthesis and deposition of perlecan and laminin. No differences were evident in the immunofluorescence for keratocan or keratan sulfate in the scar tissue, but the scar tissue did contain markedly decreased levels of lumican. Thus, the regulation of proteoglycan and glycoprotein synthesis is altered in the keratocytes that are recruited to the wounded regions in the growing corneal stroma of post-hatched young chicks. While synthesis and deposition of adhesive molecules including laminin and perlecan are elevated, the synthesis of one of the keratan sulfate proteoglycans, lumican, is reduced in the scar tissue as compared to the normally growing stroma.

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Year:  1998        PMID: 9820791     DOI: 10.1006/exer.1998.0540

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  15 in total

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Review 4.  The molecular basis of corneal transparency.

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8.  Enhanced detection method for corneal protein identification using shotgun proteomics.

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9.  Neonatal corneal stromal development in the normal and lumican-deficient mouse.

Authors:  Julia Song; Young-Ghee Lee; Jennifer Houston; W Matthew Petroll; Shukti Chakravarti; H Dwight Cavanagh; James V Jester
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10.  Protein expression pattern of collagen type XV in mouse cornea.

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