NOX2 in lung inflammation: quantum dot based in situ imaging of NOX2-mediated expression of vascular cell adhesion molecule-1

RL Orndorff, N Hong, K Yu… - … of Physiology-Lung …, 2014 - journals.physiology.org
RL Orndorff, N Hong, K Yu, SI Feinstein, BJ Zern, AB Fisher, VR Muzykantov, S Chatterjee
American Journal of Physiology-Lung Cellular and Molecular …, 2014journals.physiology.org
Quantum dot (QD) imaging is a powerful tool for studying signaling pathways as they occur.
Here we employ this tool to study adhesion molecule expression with lung inflammation in
vivo. A key event in pulmonary inflammation is the regulation of vascular endothelial cell
adhesion molecule-1 (VCAM), which drives activated immune cell adherence. The induction
of VCAM expression is known to be associated with reactive oxygen species (ROS)
production, but the exact mechanism or the cellular source of ROS that regulates VCAM in …
Quantum dot (QD) imaging is a powerful tool for studying signaling pathways as they occur. Here we employ this tool to study adhesion molecule expression with lung inflammation in vivo. A key event in pulmonary inflammation is the regulation of vascular endothelial cell adhesion molecule-1 (VCAM), which drives activated immune cell adherence. The induction of VCAM expression is known to be associated with reactive oxygen species (ROS) production, but the exact mechanism or the cellular source of ROS that regulates VCAM in inflamed lungs is not known. NADPH oxidase 2 (NOX2) has been reported to be a major source of ROS with pulmonary inflammation. NOX2 is expressed by both endothelial and immune cells. Here we use VCAM-targeted QDs in a mouse model to show that NOX2, specifically endothelial NOX2, induces VCAM expression with lung inflammation in vivo.
American Physiological Society
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