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Published ahead of print on August 28, 2003, doi:10.1164/rccm.200304-562OC
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American Journal of Respiratory and Critical Care Medicine Vol 168. pp. 1391-1398, (2003)
© 2003 American Thoracic Society

Stretch Activates Nitric Oxide Production in Pulmonary Vascular Endothelial Cells In Situ

Wolfgang M. Kuebler, Ulrike Uhlig, Torsten Goldmann, Gregor Schael, Alexander Kerem, Kay Exner, Christian Martin, Ekkehard Vollmer and Stefan Uhlig

Division of Pulmonary Pharmacology, Research Center Borstel, Borstel; Institute of Physiology, Free University of Berlin; and Institute of Anesthesiology, Deutsches Herzzentrum Berlin, Berlin, Germany

Correspondence and requests for reprints should be addressed to Stefan Uhlig, Ph.D., Division of Pulmonary Pharmacology, Research Center Borstel, Parkallee 22, 23845 Borstel, Germany. E-mail: suhlig{at}fz-borstel.de

Whereas endothelial responses to shear stress have been studied extensively, the responses to circumferential vascular stretch are yet poorly defined. Circumferential stretch in pulmonary microvessels is largely determined by the transmural pressure gradient, hence by both vascular perfusion and alveolar ventilation pressures. Here, we have studied the production of nitric oxide (NO) by the endothelial nitric oxide synthase (eNOS) in two different models of vascular stretch in the intact lung: In isolated-perfused rat lungs, vascular stretch was induced by elevation of vascular pressure. In situ digital fluorescence microscopy revealed stretch-dependent NO production, which was localized to capillary endothelial cells and inhibited by NOS blockers. In isolated-perfused mouse lungs, vascular stretch was generated by ventilation with elevated negative pressure. Stretch-induced phosphorylation of Akt and eNOS in lung endothelial cells was demonstrated by immunohistochemistry and increased NO production by in situ fluorescence microscopy. Stretch-induced endothelial responses in both models were abrogated by pretreatment with phosphatidylinositol-3-OH kinase inhibitors. These findings demonstrate that circumferential stretch activates NO production in pulmonary endothelial cells by a signaling cascade involving phosphatidylinositol-3-OH kinase, Akt, and eNOS and that this response is independent from the mechanical factors causing vascular distension.

Key Words: overventilation • hydrostatic stress • fluorescence microscopy • endothelial nitric oxide synthase • phosphatidylinositol-3-OH kinase




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