scholarly journals Involvement of Toll-Like Receptor 4 in Decreased Vasopressor Response Following Trauma/Hemorrhagic Shock: Erratum

2022 ◽  
Vol 4 (1) ◽  
pp. e0609
2005 ◽  
Vol 201 (3) ◽  
pp. S36
Author(s):  
Kinga A. Powers ◽  
Katalin Szaszi ◽  
Rachel Khadaroo ◽  
Patrick Tawadros ◽  
John C. Marshall ◽  
...  

2005 ◽  
Vol 288 (3) ◽  
pp. R600-R606 ◽  
Author(s):  
Xianzhong Meng ◽  
Lihua Ao ◽  
Yong Song ◽  
Christopher D. Raeburn ◽  
David A. Fullerton ◽  
...  

Hemorrhagic shock causes myocardial contractile depression. Although this myocardial disorder is associated with increased expression of tumor necrosis factor-α (TNF-α), the role of TNF-α as a myocardial depressant factor in hemorrhagic shock remains to be determined. Moreover, it is unclear which TNF-α receptor mediates the myocardial depressive effects of TNF-α. Toll-like receptor 4 (TLR4) regulates cellular expression of proinflammatory mediators following lipopolysaccharide stimulation and may be involved in the tissue inflammatory response to injury. The contribution of TLR4 signaling to tissue TNF-α response to hemorrhagic shock and TLR4’s role in myocardial depression during hemorrhagic shock are presently unknown. We examined the relationship of TNF-α production to myocardial depression in a mouse model of nonresuscitated hemorrhagic shock, assessed the influence of TLR4 mutation, resulting in defective signaling, on TNF-α production and myocardial depression, and determined the roles of TNF-α and TNF-α receptors in myocardial depression using a gene knockout (KO) approach. Hemorrhagic shock resulted in increased plasma and myocardial TNF-α (4.9- and 4.5-fold, respectively) at 30 min and induced myocardial contractile depression at 4 h. TLR4 mutation abolished the TNF-α response and attenuated myocardial depression (left ventricular developed pressure of 43.0 ± 6.2 mmHg in TLR4 mutant vs. 30.0 ± 3.6 mmHg in wild type, P < 0.05). TNF-α KO also attenuated myocardial depression in hemorrhagic shock, and the p55 receptor KO, but not the p75 receptor KO, mimicked the effect of TNF-α KO. The results suggest that TLR4 plays a novel role in signaling to the TNF-α response during hemorrhagic shock and that TNF-α through the p55 receptor activates a pathway leading to myocardial depression. Thus TLR4 and the p55 TNF-α receptor represent therapeutic targets for preservation of cardiac mechanical function during hemorrhagic shock.


2002 ◽  
Vol 168 (10) ◽  
pp. 5252-5259 ◽  
Author(s):  
Jie Fan ◽  
Andras Kapus ◽  
Philip A. Marsden ◽  
Yue Hua Li ◽  
George Oreopoulos ◽  
...  

Shock ◽  
2003 ◽  
Vol 19 (Supplement) ◽  
pp. 25
Author(s):  
K Powers ◽  
K Szaszi ◽  
R Khadaroo ◽  
G Papia ◽  
A Kapus ◽  
...  

2006 ◽  
Vol 202 (3) ◽  
pp. 407-417 ◽  
Author(s):  
Jose M. Prince ◽  
Ryan M. Levy ◽  
Runkuan Yang ◽  
Kevin P. Mollen ◽  
Mitchell P. Fink ◽  
...  

2006 ◽  
Vol 203 (8) ◽  
pp. 1951-1961 ◽  
Author(s):  
Kinga A. Powers ◽  
Katalin Szászi ◽  
Rachel G. Khadaroo ◽  
Patrick S. Tawadros ◽  
John C. Marshall ◽  
...  

Oxidative stress generated by ischemia/reperfusion is known to prime inflammatory cells for increased responsiveness to subsequent stimuli, such as lipopolysaccharide (LPS). The mechanism(s) underlying this effect remains poorly elucidated. These studies show that alveolar macrophages recovered from rodents subjected to hemorrhagic shock/resuscitation expressed increased surface levels of Toll-like receptor 4 (TLR4), an effect inhibited by adding the antioxidant N-acetylcysteine to the resuscitation fluid. Consistent with a role for oxidative stress in this effect, in vitro H2O2 treatment of RAW 264.7 macrophages similarly caused an increase in surface TLR4. The H2O2-induced increase in surface TLR4 was prevented by depleting intracellular calcium or disrupting the cytoskeleton, suggesting the involvement of receptor exocytosis. Further, fluorescent resonance energy transfer between TLR4 and the raft marker GM1 as well as biochemical analysis of the raft components demonstrated that oxidative stress redistributes TLR4 to lipid rafts in the plasma membrane. Preventing the oxidant-induced movement of TLR4 to lipid rafts using methyl-β-cyclodextrin precluded the increased responsiveness of cells to LPS after H2O2 treatment. Collectively, these studies suggest a novel mechanism whereby oxidative stress might prime the responsiveness of cells of the innate immune system.


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