The pulmonary endothelium is a critical, semi-selective cellular barrier which prevents the leakage of water, solutes, macromolecules and cells from the vasculature. Disruption of lung endothelial cell integrity results in alveolar flooding, hypoxemia and multi-organ dysfunction due to increases in both endothelial cell permeability and transendothelial leukocyte migration to the lung. Both of these important inflammatory processes can be attributed to increases in paracellular gaps which form between adjacent endothelium. Our previous studies have identified an important role for endothelial cell contractile forces in paracellular gap regulation and we have cloned several novel endothelial cell contractile elements which contribute to this contractile process including a novel endothelial cell myosin light chain kinase (EC MLCK) isoform. In this proposal, we will examine novel biochemical and molecular mechanisms by which endothelial contractile forces are initiated and maintained.
Specific Aim #1 will examine the interaction between p60src kinase, the p85 kD actin-binding protein, cortactin, and EC MLCK in the context of endothelial cell cytoskeletal rearrangement.
Specific Aim #2 will determine the exact contribution of Rho family GTPases to endothelial cell myosin phosphorylation, gap formation and permeability evoked by barrier-disrupting agonists.
Specific Aim #3 will identify the contributing role of the actin- and myosin- binding protein, caldesmon, in sustained endothelial cell contraction and endothelial cell barrier regulation. The very diversity of potential pathogenetic factors involved in vascular barrier dysfunction emphasizes that there is still much to be understood about the pathophysiology of this challenging disease. We speculate that the results obtained in this competitive renewal application will significantly impact our understanding of the initiating phases (SA #1 and SA #2) and the sustained phase (SA #3) of endothelial cell contraction and barrier regulation and allow us to develop new insights into this important aspect of lung inflammation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL050533-10
Application #
6537078
Study Section
Special Emphasis Panel (ZRG1-RAP (01))
Program Officer
Gail, Dorothy
Project Start
1994-06-01
Project End
2003-02-06
Budget Start
2002-06-01
Budget End
2003-02-06
Support Year
10
Fiscal Year
2002
Total Cost
$190,939
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Bogatcheva, Natalia V; Wang, Peiyi; Birukova, Anna A et al. (2006) Mechanism of fluoride-induced MAP kinase activation in pulmonary artery endothelial cells. Am J Physiol Lung Cell Mol Physiol 290:L1139-45
Petrache, Irina; Birukov, Konstantin; Zaiman, Ari L et al. (2003) Caspase-dependent cleavage of myosin light chain kinase (MLCK) is involved in TNF-alpha-mediated bovine pulmonary endothelial cell apoptosis. FASEB J 17:407-16
Schaphorst, Kane L; Chiang, Eddie; Jacobs, Keri N et al. (2003) Role of sphingosine-1 phosphate in the enhancement of endothelial barrier integrity by platelet-released products. Am J Physiol Lung Cell Mol Physiol 285:L258-67
Birukov, Konstantin G; Jacobson, Jeffrey R; Flores, Alejandro A et al. (2003) Magnitude-dependent regulation of pulmonary endothelial cell barrier function by cyclic stretch. Am J Physiol Lung Cell Mol Physiol 285:L785-97
Borbiev, Talaibek; Verin, Alexander D; Birukova, Anna et al. (2003) Role of CaM kinase II and ERK activation in thrombin-induced endothelial cell barrier dysfunction. Am J Physiol Lung Cell Mol Physiol 285:L43-54
Shikata, Yasushi; Birukov, Konstantin G; Birukova, Anna A et al. (2003) Involvement of site-specific FAK phosphorylation in sphingosine-1 phosphate- and thrombin-induced focal adhesion remodeling: role of Src and GIT. FASEB J 17:2240-9
Borbiev, T; Garcia, J G; Berin, A D (2003) [Role of phosphorylation of myosin and actin-binding proteins in endothelial permeability induced by thrombin] Bioorg Khim 29:510-7
Bogatcheva, Natalia V; Garcia, Joe G N; Verin, Alexander D (2002) Role of tyrosine kinase signaling in endothelial cell barrier regulation. Vascul Pharmacol 39:201-12
Birukov, Konstantin G; Birukova, Anna A; Dudek, Steven M et al. (2002) Shear stress-mediated cytoskeletal remodeling and cortactin translocation in pulmonary endothelial cells. Am J Respir Cell Mol Biol 26:453-64
Bogatcheva, N V; Garcia, J G N; Verin, A D (2002) Molecular mechanisms of thrombin-induced endothelial cell permeability. Biochemistry (Mosc) 67:75-84

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