2015
DOI: 10.1089/jir.2014.0188
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Interferon-Gamma Increases Endothelial Permeability by Causing Activation of p38 MAP Kinase and Actin Cytoskeleton Alteration

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Cited by 43 publications
(26 citation statements)
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“…In this study, the highest aortic endothelial cell permeability was observed at 10 ng/ml of TNF-α and 24 h of incubation period. Our result is in agreement with cytokineinduced increased permeability in human umbilical vein endothelial cells (McKenzie & Ridley, 2007;Ng et al, 2015). However, we found that TNF-α exerted a direct toxic effect on HAEC after incubated for 24 h. This is consistent with previous studies that demonstrated the apoptotic effect of TNF-α in endothelial cells (Aveleira et al, 2010;Petrache et al, 2001).…”
Section: Discussionsupporting
confidence: 93%
“…In this study, the highest aortic endothelial cell permeability was observed at 10 ng/ml of TNF-α and 24 h of incubation period. Our result is in agreement with cytokineinduced increased permeability in human umbilical vein endothelial cells (McKenzie & Ridley, 2007;Ng et al, 2015). However, we found that TNF-α exerted a direct toxic effect on HAEC after incubated for 24 h. This is consistent with previous studies that demonstrated the apoptotic effect of TNF-α in endothelial cells (Aveleira et al, 2010;Petrache et al, 2001).…”
Section: Discussionsupporting
confidence: 93%
“…Mechanistically, IL-9 regulated the IFN-g-and IL-17A-mediated physical properties (stress fibers formation, contractility, and stiffness) of human keratinocytes. Similar to our study, previous studies have shown the effect of IFN-g on actin cytoskeleton reorganization in various cell types (41). Similar to human keratinocytes, IL-9 suppressed the IFNgand IL-17A-induced migration of epidermoid carcinoma cells (A-431).…”
Section: Discussionsupporting
confidence: 91%
“…IFN-γ can also act on T cells, orchestrating CD4 + T cell and CD8 + T cell activation and differentiation, as well as apoptosis ( 18 24 ). Moreover, IFN-γ can directly modify the function and status of brain-resident and -specialized cell populations, including neurons, brain endothelial cells, microglial cells, and astrocytes, in a variety of inflammatory settings, including malaria ( 25 30 ). Combined, these observations indicate that IFN-γ may mediate ECM development by targeting a specific cell type, in a particular location, at a precise time of infection.…”
Section: Introductionmentioning
confidence: 99%