CELL-SPECIFIC EXPRESSION OF FIBRONECTIN AND EIIIA AND EIIIB SPLICE VARIANTS AFTER OXYGEN INJURY

Citation
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
Citations number
35
Categorie Soggetti
Physiology
ISSN journal
10400605
Volume
18
Issue
4
Year of publication
1998
Pages
599 - 609
Database
ISI
SICI code
1040-0605(1998)18:4<599:CEOFAE>2.0.ZU;2-G
Abstract
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.