Published ahead of print on August 4, 2005, doi:10.1164/rccm.200504-605OC
American Journal of Respiratory and Critical Care Medicine Vol 172. pp. 1119-1127, (2005)
© 2005 American Thoracic Society
doi: 10.1164/rccm.200504-605OC
Lung-marginated Monocytes Modulate Pulmonary Microvascular Injury during Early Endotoxemia
Kieran P. O'Dea,
Arnold J. Young,
Hirotoshi Yamamoto,
James L. Robotham,
Fionula M. Brennan and
Masao Takata
Department of Anesthetics and Intensive Care, and Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College London, London, United Kingdom; and Department of Anesthesiology, University of Rochester Medical Center, Rochester, New York
Correspondence and requests for reprints should be addressed to Dr. Masao Takata, M.D., Ph.D., Department of Anaesthetics and Intensive Care, Imperial College London, Chelsea and Westminster Hospital, 369 Fulham Road, London SW10 9NH, UK. E-mail: m.takata{at}imperial.ac.uk
Rationale: The role of monocytes in acute endotoxemia has been ascribed to systemic release of mediators within the central circulation. Little is known about the potential role of "marginated" monocytes in regulating microvascular inflammatory signaling. Objectives: To investigate whether lung-marginated monocytes can locally activate pulmonary endothelial cells through cell contact–dependent interactions in early endotoxemia. Methods: Mice were challenged with LPS to produce acute endotoxemia and pulmonary vascular injury. Adoptive transfer of ex vivo LPS-stimulated donor leukocytes to recipient mice was also performed to evaluate cell-associated inflammatory signaling between monocytes and endothelial cells within the lung. Cell suspensions from excised lungs were analyzed by flow cytometry for expression of tumor necrosis factor  (TNF-) on monocytes and cell adhesion molecules on endothelial cells. Results: Substantial numbers of monocytes rapidly marginated to the lungs after endotoxin challenge in mice, and lung-marginated monocytes expressed significantly higher levels of membrane TNF than circulating monocytes, due to higher TNF production by the marginated cells. Injection of activated wild-type donor leukocytes to wild-type or TNF receptor double knockout recipients demonstrated that lung-marginated monocytes can induce TNF-dependent upregulation of adhesion molecules on pulmonary endothelial cells. Injection of activated donor leukocytes from TNF knock-in mice that express uncleavable mutant membrane TNF also induced adhesion molecule upregulation in wild-type recipients without a systemic soluble TNF release. Conclusions: These results reveal a previously unacknowledged role for lung-marginated monocytes in early endotoxemia, exerting local, cell-associated TNF signaling within the pulmonary microcirculation, contributing to the evolution of pulmonary vascular injury.
Key Words: endothelial cells • endotoxin shock • lipopolysaccharide • lung • macrophages
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Copyright © 2005 American Thoracic Society
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