Am. J. Respir. Cell Mol. Biol., Vol 15, No. 5, Nov 1996, 624-632.
Epithelial barrier integrity during in vitro wound repair of the airway epithelium
AL Herard, JM Zahm, D Pierrot, J Hinnrasky, C Fuchey and E Puchelle
INSERM U314, FR53, CHR Maison-Blanche, Reims, France.
The surface epithelium of the airway mucosa forms a continuous barrier to a
wide number of noxious substances present in the lumen. The restoration of
the barrier integrity after injury represents a key issue in the defense
capacity of the airway epithelium. Using an in vitro wound repair model of
the airway epithelium, we investigated the dynamic of the restoration of
the epithelial barrier integrity during the wound repair process. Airway
epithelial cells in culture were chemically wounded by sodium hydroxide.
The immunolocalization of zonula occludens 1 (ZO-1), a cytoplasmic protein
associated with the tight junctions, was examined during the wound repair
process. Junctional integrity was examined by analyzing the transepithelial
resistance (TER) and the permeability to [3H]mannitol and by visualizing
the permeability to lanthanum nitrate during 5 days after injury.
Immediately after injury, we simultaneously observed a 36.7% decrease in
the TER and a 74.9% rise in the permeability to [3H]mannitol. In addition,
lanthanum nitrate penetrated in the intercellular spaces in the repairing
areas, which was also characterized by the absence of ZO-1 staining, as
opposed to nonrepairing cells. TER and [3H]mannitol flux values as well as
lanthanum nitrate and ZO-1 localizations were found to be similar to those
observed in confluent cultures only 1 to 2 days after complete wound
closure. This study demonstrates that using our culture model, confluent
airway epithelial cells form a continuous and efficient barrier with tight
junctions. Epithelial integrity is affected immediately after injury and is
completely restored within 1 to 2 days after wound closure. During such a
period of time, the airway epithelium may remain exposed to the noxious
effect of environment in vivo, which can prevent the epithelial barrier
restoration by modifying tight junction formation.
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Copyright © 1996 American Thoracic Society.
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