Aims: Our overall aim is to understand the in situ biology of lung endothelial cells (EC) in relation to the initiation of lung inflammation. We reported that mitochondrial H2O2 determines endothelial proinflammatory activation. Here, we will determine modification of the H2O2 effect by nitric oxide (NO).
The specific aims are to determine in EC of lung capillaries (i) the extent to which NO modifies reactive oxygen species (ROS) formation, and (ii) NO-ROS interactions determining cell-surface expression of P-selectin and TNFalpha receptor type 1. Procedures: We will use the isolated, blood-perfused lung preparation for mouse and rat. Arteriolar, septal and venular capillaries will be loaded with specific fluorophores for the detection of cytosolic, mitochondrial and endosomal store Ca2+, for ROS and NO production and for detection of expression and shedding of P-selectin and TNFR1. Single EC in these capillaries will be optically imaged in real-time by of wide-angle and confocal microscopy. For proinflammatory activation, the capillaries will be challenged with TNFalpha, high capillary pressure, arachidonate and photolytic uncaging of Ca2+. EC responses will be determined with regard to NO and ROS production, and the expression and shedding of the P-selectin and TNFR1. The hypotheses will also be tested in mice containing genetically defective NAD(P)H oxidase (gp91phox(-/-)), and mice deficient in eNOS, iNOS and TNFR1. The data will be processed by means of image analysis software. Significance: Although NO-ROS interactions are well studied in the pathological context, the extent to which such interactions regulate physiological responses of the lung capillary remains unclear. Our research will reveal for the first time, interactions between NO and ROS of mitochondrial and NAD(P)H oxidase origins, in the initiation of proinflammatory events in lung capillaries. We will understand the role of these interactions in regulating proinflammatory receptor expression. These considerations will advance the understanding of the inception of lung inflammation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL057556-11
Application #
7265114
Study Section
Lung Cellular, Molecular, and Immunobiology Study Section (LCMI)
Program Officer
Golden, AL
Project Start
1997-09-12
Project End
2007-11-30
Budget Start
2007-08-01
Budget End
2007-11-30
Support Year
11
Fiscal Year
2007
Total Cost
$131,605
Indirect Cost
Name
St. Luke's-Roosevelt Institute for Health Sciences
Department
Type
DUNS #
623216371
City
New York
State
NY
Country
United States
Zip Code
10019
Sinha, Pratik; Islam, Mohammad N; Bhattacharya, Sunita et al. (2016) Intercellular mitochondrial transfer: bioenergetic crosstalk between cells. Curr Opin Genet Dev 38:97-101
Bhattacharya, Jahar; Westphalen, Kristin (2016) Macrophage-epithelial interactions in pulmonary alveoli. Semin Immunopathol 38:461-9
Westphalen, Kristin; Gusarova, Galina A; Islam, Mohammad N et al. (2014) Sessile alveolar macrophages communicate with alveolar epithelium to modulate immunity. Nature 506:503-6
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Huertas, Alice; Das, Shonit R; Emin, Memet et al. (2013) Erythrocytes induce proinflammatory endothelial activation in hypoxia. Am J Respir Cell Mol Biol 48:78-86
Bhattacharya, Jahar; Matthay, Michael A (2013) Regulation and repair of the alveolar-capillary barrier in acute lung injury. Annu Rev Physiol 75:593-615
Emin, Memet T; Sun, Li; Huertas, Alice et al. (2012) Platelets induce endothelial tissue factor expression in a mouse model of acid-induced lung injury. Am J Physiol Lung Cell Mol Physiol 302:L1209-20
Quadri, Sadiqa K; Sun, Li; Islam, Mohammad Naimul et al. (2012) Cadherin selectivity filter regulates endothelial sieving properties. Nat Commun 3:1099
Islam, Mohammad Naimul; Das, Shonit R; Emin, Memet T et al. (2012) Mitochondrial transfer from bone-marrow-derived stromal cells to pulmonary alveoli protects against acute lung injury. Nat Med 18:759-65
Parthasarathi, Kaushik; Bhattacharya, Jahar (2011) Localized acid instillation by a wedged-catheter method reveals a role for vascular gap junctions in spatial expansion of acid injury. Anat Rec (Hoboken) 294:1585-91

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