|
|
||||||||
AJP - Lung Cellular and Molecular Physiology, Vol 265, Issue 5 485-L492, Copyright © 1993 by American Physiological Society
ARTICLES |
P. A. Vincent, R. A. Rebres, E. P. Lewis, V. Hurst 4th and T. M. Saba
Department of Physiology and Cell Biology, Albany Medical College of Union University, New York 12208.
Fibronectin (Fn) is an adhesive protein found in the plasma and extracellular tissue matrix. Locally synthesized tissue or cellular Fn (cFn) has extra domains (ED1 and ED2) not present in liver synthesized plasma Fn (pFn). In the lung, Fn is found in the endothelial and epithelial basement membranes, as well as in the interstitial matrix. Utilizing murine monoclonal antibodies to ED1 of cFn, we studied the release of total Fn as well as ED1-Fn into the plasma-free perfusate of the isolated perfused rabbit lung in relation to changes in lung weight due to fluid accumulation after oxidant (H2O2) challenge. Both parameters were also studied after addition of cycloheximide (20 micrograms/ml perfusate) to the perfusion medium to inhibit lung protein synthesis. After continuous H2O2 challenge (11 nmol.ml buffer-1.min-1), there was a 2.25 +/- 0.62 g increase in lung weight over 60 min. Measurement of 125I-labeled albumin clearance at 20 min after the start of H2O2 infusion confirmed an increase in lung endothelial protein permeability after H2O2 treatment. Fn antigen was released into the perfusate as early as 15 min after oxidant challenge. By 60 min, total perfusate Fn increased in H2O2-treated lungs (n = 6) to 2.10 +/- 0.48 micrograms/ml compared with only 0.35 +/- 0.09 micrograms/ml in normal control lungs (n = 5). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of nonreduced samples revealed that the Fn released consisted of primarily intact (440 kDa) Fn as well as Fn fragments. A rapid release of ED1-Fn paralleled the increased release of total Fn.(ABSTRACT TRUNCATED AT 250 WORDS)
This article has been cited by other articles:
![]() |
D. Mehta and A. B. Malik Signaling Mechanisms Regulating Endothelial Permeability Physiol Rev, January 1, 2006; 86(1): 279 - 367. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. B. Waypa, C. A. Morton, P. A. Vincent, J. R. Mahoney Jr., W. K. Johnston III, and F. L. Minnear Oxidant-increased endothelial permeability: prevention with phosphodiesterase inhibition vs. cAMP production J Appl Physiol, March 1, 2000; 88(3): 835 - 842. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Mourgeon, J. Xu, A. K. Tanswell, M. Liu, and M. Post Mechanical strain-induced posttranscriptional regulation of fibronectin production in fetal lung cells Am J Physiol Lung Cell Mol Physiol, July 1, 1999; 277(1): L142 - L149. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. M. Curtis, R. F. Rotundo, P. A. Vincent, P. J. McKeown-Longo, and T. M. Saba TNF-alpha -induced matrix Fn disruption and decreased endothelial integrity are independent of Fn proteolysis Am J Physiol Lung Cell Mol Physiol, July 1, 1998; 275(1): L126 - L138. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |