抄録
In order to modulate palatal scar tissue, especially its myofibroblastic component, there is a
pressing need for an in vitro model of this tissue. In the present, study we established an organ
culture model of the rat palatal scar tissue. After excision of palatal mucoperiosteum, explants
from the developing immature scar tissue and from the normal palatal mucosa were used to observe
myofibroblasts in vivo and their maintenance in organ culture. Explants were cultured at the gasliquid
interface in serum-free Waymouth's MB 752/1 medium and in a humid atmosphere containing 55%
O2/5% C02 in air at 37℃ for 3 days.
Viability of the cultured explants was evaluated with morphological and histological criteria and
BrdU incorporation. After organ culture, the scar tissue showed good preservation of the in vivo
histology. The myofibroblasts and smooth muscle cells of the cultured scar tissues showed
continuous expression of alpha-smooth muscle actin (α-SMA), mimicking the in vivo situation.
In the normal tissues, only smooth muscle cells of the blood
vessels expressed α-SMA. These results demonstrate that the established model provides a useful
in vitro experimental tool for investigating the
palatal scar tissue in general and its myofibroblasts in particular.