Conjunctival expression of thymosin-â4 in vernal keratoconjunctivitis. (Articolo in rivista)

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  • Conjunctival expression of thymosin-â4 in vernal keratoconjunctivitis. (Articolo in rivista) (literal)
Anno
  • 2006-01-01T00:00:00+01:00 (literal)
Alternative label
  • Micera A. 1,4, Bonini S.2,3, Lambiase A.1,4, Lapucci G.2, Bonini S.1,4, Rasi G.2 (2006)
    Conjunctival expression of thymosin-â4 in vernal keratoconjunctivitis.
    in Molecular vision
    (literal)
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  • Micera A. 1,4, Bonini S.2,3, Lambiase A.1,4, Lapucci G.2, Bonini S.1,4, Rasi G.2 (literal)
Pagina inizio
  • 1594 (literal)
Pagina fine
  • 1600 (literal)
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  • 12 (literal)
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Note
  • ISI Web of Science (WOS) (literal)
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  • 1 Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS)-Gian Battista Bietti Eye Foundation, Rome, Italy; 2 Institute of Neurobiology and Molecular Medicine, National Research Council (INMM-CNR), Rome, Italy; 3 Second University of Naples, Naples, Italy; 4CIR, Laboratory of Ophthalmology, University Campus Bio-Medico, Rome, Italy (literal)
Titolo
  • Conjunctival expression of thymosin-â4 in vernal keratoconjunctivitis. (literal)
Abstract
  • Purpose: Thymosin-â4 (Tâ4) is a small actin-sequestrating peptide that modulates inflammation and healing in different tissues. The aim of this study was to investigate the molecular and biochemical expression of Tâ4 in the healthy conjunctiva and in the conjunctiva of patients with vernal keratoconjunctivitis (VKC), a severe allergic eye disease characterized by chronic inflammation and marked tissue remodeling. Methods: Conjunctival tissues, obtained from seven VKC patients and five sex/age-matched healthy subjects, were evaluated for Tâ4 expression by relative real time-PCR and light/confocal microscopy. The distribution patterns of Tâ4 in conjunctival sections as well as Tâ4 expression by mast cells (AA1), eosinophils (EG2), and fibroblast/myofibroblasts (Thy1/á-SMA) in VKC tissues was also evaluated by double immunofluorescence. Results: Compared to healthy specimens, Tâ4 mRNA appeared upregulated in VKC conjunctival biopsies as detected by real-time PCR. In the healthy conjunctiva, Tâ4 protein expression was confined to the conjunctival epithelium, while a weak staining was observed in the stroma. In VKC conjunctival sections, Tâ4 immunoreactivity was selectively increased in the stroma where, by confocal analysis of VKC papillary formations, Tâ4 appeared to be mostly localized in eosinophils and activated fibroblasts/myofibroblasts. Conclusions: Our data provides the first evidence of Tâ4 expression in the conjunctival tissues. The upregulation of both Tâ4 mRNA and protein in the conjunctival stroma, and its peculiar localization in eosinophils and myofibroblasts populating VKC lesions, suggest a possible role for Tâ4 in tissue inflammation and remodeling occurring in VKC. (literal)
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