Literature DB >> 1376216

Expression of vimentin by rabbit corneal epithelial cells during wound repair.

N SundarRaj1, J D Rizzo, S C Anderson, J P Gesiotto.   

Abstract

Intermediate filaments of epithelial cells generally consist of specific combinations of keratins. However, cultured epithelial cells from certain tissues and some epithelial tumors have been shown also to express vimentin. In the present study, the expression of vimentin by epithelial cells in healing corneal wounds (partial thickness penetrating wounds) and in tissue culture was analyzed. Both immunohistochemical and immunotransblot analyses indicated that although vimentin was not detected in the normal rabbit corneal epithelium in vivo, cultured rabbit corneal epithelial cells co-express keratins and vimentin. At 1 day post-wounding, vimentin was not detectable in the epithelial cells that had covered the denuded stroma. However, at 2 days postwounding, the epithelium at the base of the epithelial plug immunoreacted with both anti-vimentin and antikeratin monoclonal antibodies. Immunotransblot analyses of the extracts of the epithelial plugs confirmed the presence of vimentin (Mr = 58k). The 58k band was not detected in the extract of normal rabbit corneal epithelium. At day/5, vimentin was no longer detectable in the epithelium. This study demonstrated that corneal epithelial cells transiently co-express vimentin and keratins in vivo during wound healing and in tissue culture. The time-course of the transient expression of vimentin suggests that the vimentin expression in the epithelial cells during healing is not linked to cell proliferation or to the centripetal migration of the epithelium during early stages (first 24 h) of healing, but may be linked to cell-matrix interactions or the migration of basal cells in the upward direction at the following stage of healing.

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Year:  1992        PMID: 1376216     DOI: 10.1007/bf00302973

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  48 in total

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Journal:  Nature       Date:  1983 Jun 23-29       Impact factor: 49.962

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Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

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  16 in total

1.  The gene expression sequence of radiated mucosa in an animal mucositis model.

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Journal:  Cell Prolif       Date:  2002-08       Impact factor: 6.831

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Journal:  Invest Ophthalmol Vis Sci       Date:  2007-02       Impact factor: 4.799

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Authors:  Shun-Ichi Imamura; Joe C Adams
Journal:  J Assoc Res Otolaryngol       Date:  2003-06

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Authors:  D Biddle; D F Spandau
Journal:  Arch Dermatol Res       Date:  1996-09       Impact factor: 3.017

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Authors:  Sabine Ladrech; Michel Eybalin; Jean-Luc Puel; Marc Lenoir
Journal:  Histochem Cell Biol       Date:  2017-04-01       Impact factor: 4.304

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Authors:  Federico Castro-Muñozledo; Cristina Velez-DelValle; Meytha Marsch-Moreno; Miriam Hernández-Quintero; Walid Kuri-Harcuch
Journal:  Histochem Cell Biol       Date:  2014-08-21       Impact factor: 4.304

7.  The stromal proteinase MMP3/stromelysin-1 promotes mammary carcinogenesis.

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Journal:  Cell       Date:  1999-07-23       Impact factor: 41.582

8.  Vimentin is sufficient and required for wound repair and remodeling in alveolar epithelial cells.

Authors:  Micah R Rogel; Pritin N Soni; James R Troken; Albert Sitikov; Humberto E Trejo; Karen M Ridge
Journal:  FASEB J       Date:  2011-07-29       Impact factor: 5.191

9.  Co-localization of vimentin and cytokeratins in M-cells of rabbit gut-associated lymphoid tissue (GALT).

Authors:  A Gebert; G Hach; H Bartels
Journal:  Cell Tissue Res       Date:  1992-08       Impact factor: 5.249

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Authors:  A Gebert; G Hach
Journal:  Histochemistry       Date:  1992-11
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