Augmentation of Nitric Oxide Production by Gamma Interferon in a Mouse Vascular Endothelial Cell Line and Its Modulation by Tumor Necrosis Factor Alpha and Lipopolysaccharide

2000 ◽  
Vol 68 (11) ◽  
pp. 6209-6214
Author(s):  
Akiko Morikawa ◽  
Naoki Koide ◽  
Yutaka Kato ◽  
Tsuyoshi Sugiyama ◽  
Dipshikha Chakravortty ◽  
...  
2006 ◽  
Vol 281 (1-2) ◽  
pp. 123-128 ◽  
Author(s):  
Luiz Fernando de Souza ◽  
Daniel Pens Gelain ◽  
Fernanda Rafaela Jardim ◽  
Gisele Roncheti Ribeiro ◽  
Marcelo Zim ◽  
...  

1990 ◽  
Vol 258 (2) ◽  
pp. L57-L67 ◽  
Author(s):  
S. E. Goldblum ◽  
W. L. Sun

Tumor necrosis factor-alpha (TNF alpha) has been implicated as a mediator of pulmonary vascular endothelial injury. We studied the effect of human recombinant TNF alpha (rTNF alpha) on transfer of 14C-labeled bovine serum albumin (BSA) across cultured bovine pulmonary arterial endothelial cell monolayers. rTNF alpha induced a dose-, time-, and temperature-dependent increment in transendothelial [14C]BSA flux. Only after an incubation time of greater than or equal to 4 h did rTNF alpha significantly (P less than 0.005) increase transendothelial albumin flux. rTNF alpha exposure times as brief as 5 min induced significantly (P less than 0.005) increased albumin transfer at 6 h. Although this initial rTNF alpha-endothelial interaction was not temperature dependent, the subsequent barrier dysfunction could only be generated at 37 degrees C. The rTNF alpha-induced changes could not be ascribed to endothelial cell cytotoxicity and was not blocked by protein synthesis inhibition. The effects of rTNF alpha on endothelial permeability were reversible and not specific for albumin transfer. Therefore, rTNF alpha may influence the movement of macromolecules across the pulmonary vascular endothelial barrier.


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