Wm. Maniscalco et al., CELL-SPECIFIC EXPRESSION OF FIBRONECTIN AND EIIIA AND EIIIB SPLICE VARIANTS AFTER OXYGEN INJURY, American journal of physiology. Lung cellular and molecular physiology, 18(4), 1998, pp. 599-609
Cellular fibronectin (cFN) expression is characteristic of injured tis
sues. Unlike plasma FN, cFN mRNA often contains the EIILA or EIIIB dom
ains. We examined the lung cell-specific expression of total cFN mRNA.
and the EIIIA and EIIIB splice variants in rabbits after acute oxygen
injury. By in situ hybridization, control lung had low cFN mRNA. Afte
r exposure to >95% oxygen, mRNAs for total cFN and EIIIA were noted pr
imarily in alveolar macrophages and large-vessel endothelial cells. By
3-5 days recovery, cFN and EIIIA mRNA abundance was increased in alve
olar septal cells (i.e., alveolar epithelial, interstitial, or endothe
lial cells) and in some large-vessel endothelial cells but was low in
bronchial epithelial cells. During recovery, EIIIB mRNA was low in alv
eolar septal cells but was noted mainly in chondrocytes. Immunostainin
g for EIIIA increased during recovery, paralleling the in situ hybridi
zations. Because FN may modulate alveolar type II cell phenotype, we i
nvestigated type II cell cFN mRNA expression in vivo. During recovery,
neither isolated type II cells nor cells with surfactant protein C mR
NA in vivo contained FN mRNA. In summary, these data suggest that cFN
with the EIIIA domain has a role in alveolar cell recovery from oxygen
injury and that type II cells do not express cFN during recovery.