Ultrastructural immunocytochemical localization of fibronectin deposition during corneal endothelial wound repair. Evidence for cytoskeletal involvement

• Published in: Biology of the cell 1989, Vol.65 (2), p.171-179
• Main Authors: Sabet, Minu D., Gordon, Sheldon R.
• Format: Article
• Language: English
• Subjects: Animals; Cornea - metabolism; Cornea - ultrastructure; corneal endothelium; Corneal Injuries; Cytoskeleton - metabolism; Cytoskeleton - ultrastructure; fibronectin; Fibronectins - metabolism; Freezing; immunocytochemistry; Immunohistochemistry; Microscopy, Electron; Rats; Rats, Inbred Strains; Time Factors; wound repair
• ISSN: 0248-4900; 1768-322X
• DOI: 10.1111/j.1768-322X.1989.tb00786.x

The distribution of the extracellular matrix (ECM) protein, fibronectin (FN), has been examined ultrastructurally in noninjured and injured rat corneal endothelium in vivo and in vitro by immunoperoxidase cytochemistry. In noninjured endothelia, FN was observed within the rough endoplasmic reticulum (RER) cisternae but not along the cell‐Descemet's membrane (DM) interface. Twenty‐four and 48 h after a circular freeze injury, immunoperoxidase reaction product was detected at the cell‐DM interface as well as within cytoplasmic vesicles and intercellular spaces. By 1 and 2 wk post‐injury, a line of reaction product could still be demonstrated at the cell‐DM interface and evidence for newly deposited basement membrane material was observed in this region. In order to understand whether fibronectin deposition during wound repair was dependent on cytoskeletal influences, organ culture experiments were performed in which the media was supplemented with either 10−8M colchicine or 2.5 × 10−3M cytochalasin B. Without inhibitors, injured corneas cultured for 24 h had FN deposition at the cell‐DM interface similar to the in vivo results. Corneas cultured in the presence of cytochalasin B also showed FN deposition at the cell‐DM interface. However, when injured endothelia were cultured in the presence of colchicine, no reaction product was observed at the cell‐DM interface, although it could be detected intracellularly within RER. Incubating the tissues in the presence of puromycin abolished all extracellular and intracellular staining. These results indicate that during wound repair, corneal endothelial cells produce fibronectin and deposit it upon Descemet's membrane by a mechanism that may be mediated by microtubules.