Literature DB >> 18158589

Expression and distribution of junctional adhesion molecule-1 in the human cornea.

Lizhong Chen1, Nobuyuki Ebihara, Keiko Fujiki, Akira Murakami.   

Abstract

PURPOSE: To investigate the expression and distribution of junctional adhesion molecule 1 (JAM-1) in human corneal tissue and cells.
METHODS: Reverse transcriptase-polymerase chain reaction was used to detect the expression of JAM-1, ZO-1, and occludin mRNAs in corneal cells, while the presence of JAM-1 protein was analyzed by flow cytometry (FACS). Double immunofluorescence staining was used to determine the tissue distribution of JAM-1 and occludin in human corneas.
RESULTS: Strong expression of JAM-1, ZO-1, and occludin mRNAs was observed in primary cultured corneal epithelial and endothelial cells, but not in primary cultured keratocytes. The expression of JAM-1 protein in cultured epithelial and endothelial cells was confirmed by FACS. When keratocytes were cultured in medium with 10% fetal calf serum for several passages, differentiation into corneal myofibroblasts occurred. The expression of JAM-1 was detected in these corneal myofibroblasts at both RNA and protein levels. JAM-1 immunoreactivity was seen at cell borders throughout the entire epithelium, but not in keratocytes from normal corneal tissue. On the other hand, JAM-1 immunoreactivity was detected in the cytoplasm of corneal endothelial cells.
CONCLUSIONS: JAM-1 is expressed by human corneal epithelial and endothelial cells, but not by keratocytes, although its expression is induced in corneal myofibroblasts. (c) Japanese Ophthalmological Society 2007

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Year:  2007        PMID: 18158589     DOI: 10.1007/s10384-007-0479-5

Source DB:  PubMed          Journal:  Jpn J Ophthalmol        ISSN: 0021-5155            Impact factor:   2.447


  38 in total

Review 1.  Keratocyte and fibroblast phenotypes in the repairing cornea.

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Review 2.  Molecular structure of tight junctions and their role in epithelial transport.

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3.  Deletion of JAM-A causes morphological defects in the corneal epithelium.

Authors:  Liang I Kang; Yan Wang; Arthur T Suckow; Kirk J Czymmek; Vesselina G Cooke; Ulhas P Naik; Melinda K Duncan
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Review 4.  The JAM family of proteins.

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5.  Junctional Adhesion Molecules (JAMs) are differentially expressed in fibroblasts and co-localize with ZO-1 to adherens-like junctions.

Authors:  Andrew P Morris; Ahmad Tawil; Zuzana Berkova; Linda Wible; C Wayne Smith; Sonia A Cunningham
Journal:  Cell Commun Adhes       Date:  2006 Jul-Aug

6.  CD-34 stromal expression pattern in normal and altered human corneas.

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7.  The spatial organization of apical junctional complex-associated proteins in feline and human corneal endothelium.

Authors:  W M Petroll; J K Hsu; J Bean; H D Cavanagh; J V Jester
Journal:  Curr Eye Res       Date:  1999-01       Impact factor: 2.424

8.  Corneal keratocytes: phenotypic and species differences in abundant protein expression and in vitro light-scattering.

Authors:  James V Jester; Abhijit Budge; Steven Fisher; Jiying Huang
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-07       Impact factor: 4.799

9.  Altered KSPG expression by keratocytes following corneal injury.

Authors:  Eric C Carlson; I-Jong Wang; Chia-Yang Liu; Paul Brannan; Candace W C Kao; Winston W Y Kao
Journal:  Mol Vis       Date:  2003-11-21       Impact factor: 2.367

10.  Junctional adhesion molecule (JAM) binds to PAR-3: a possible mechanism for the recruitment of PAR-3 to tight junctions.

Authors:  M Itoh; H Sasaki; M Furuse; H Ozaki; T Kita; S Tsukita
Journal:  J Cell Biol       Date:  2001-08-06       Impact factor: 10.539

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  1 in total

1.  Diurnal variation of tight junction integrity associates inversely with matrix metalloproteinase expression in Xenopus laevis corneal epithelium: implications for circadian regulation of homeostatic surface cell desquamation.

Authors:  Allan F Wiechmann; Brian P Ceresa; Eric W Howard
Journal:  PLoS One       Date:  2014-11-20       Impact factor: 3.240

  1 in total

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