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Role of α1-adrenoceptor subtypes on corneal epithelial thickness and cell proliferation in mice
Author(s) -
Aytan Musayeva,
Caroline Manicam,
Andreas Steege,
Christoph Brochhausen,
Beate K. Straub,
Katharina Bell,
Norbert Pfeiffer,
Adrian Gericke
Publication year - 2018
Publication title -
ajp cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.432
H-Index - 181
eISSN - 1522-1563
pISSN - 0363-6143
DOI - 10.1152/ajpcell.00314.2018
Subject(s) - cornea , epithelium , corneal epithelium , biology , messenger rna , cell growth , cell , ultrastructure , microbiology and biotechnology , stroma , pathology , chemistry , anatomy , immunohistochemistry , immunology , medicine , gene , biochemistry , genetics , neuroscience
Adrenergic stimuli are important for corneal epithelial structure and healing. The purpose of the present study was to examine the hypothesis that the lack of a single α 1 -adrenoceptor (α 1 -AR) subtype affects corneal epithelial thickness and cell proliferation. Expression levels of α 1 -AR mRNA were determined in mouse cornea using real-time PCR. In mice devoid of one of the three α 1 -AR subtypes (α 1A -AR −/− , α 1B -AR −/− , α 1D -AR −/− ) and in wild-type controls, thickness of individual corneal layers, the number of epithelial cell layers, and average epithelial cell size were determined in cryosections. Endothelial cell density and morphology were calculated in corneal explants, and epithelial cell proliferation rate was determined with immunofluorescence microscopy. Moreover, the ultrastructure of the corneal epithelium was examined by transmission electron microscopy. Messenger RNA for all three α 1 -AR subtypes was expressed in whole cornea and in corneal epithelium from wild-type mice with a rank order of abundance of α 1A ≥ α 1B > α 1D . In contrast, no α 1 -AR mRNA was detected in the stroma, and only α 1B -AR mRNA was found in the Descemet endothelial complex. Remarkably, corneal epithelial thickness and mean epithelial cell size were reduced in α 1A -AR −/− mice. Our findings suggest that the α 1A -AR exerts growth effects in mouse corneal epithelial cells.

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