Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils

Role of HMGB1-TLR4 signaling

Jie Fan, Yuehua Li, Ryan M. Levy, Janet J. Fan, David Hackam, Yoram Vodovotz, Huan Yang, Kevin J. Tracey, Timothy R. Billiar, Mark A. Wilson

Research output: Contribution to journalArticle

Abstract

Hemorrhagic shock/resuscitation (HS/R)-induced generation of reactive oxygen species (ROS) plays an important role in posthemorrhage inflammation and tissue injury. We have recently reported that HS/R-activated neutrophils (PMN), through release of ROS, serve an important signaling function in mediating alveolar macrophage priming and lung inflammation. PMN NAD(P)H oxidase has been thought to be an important source of ROS following HS/R. TLR4 sits at the interface of microbial and sterile inflammation by mediating responses to both bacterial endotoxin and multiple endogenous ligands, including high-mobility group box 1 (HMGB1). Recent studies have implicated HMGB1 as an early mediator of inflammation after HS/R and organ ischemia/ reperfusion. In the present study, we tested the hypothesis that HS/R activates NAD(P)H oxidase in PMN through HMGB1/TLR4 signaling. We demonstrated that HS/R induced PMN NAD(P)H oxidase activation, in the form of phosphorylation of p47phox subunit of NAD(P)H oxidase, in wild-type mice; this induction was significantly diminished in TLR4-mutant C3H/HeJ mice. HMGB1 levels in lungs, liver, and serum were increased as early as 2 h after HS/R. Neutralizing Ab to HMGB1 prevented HS/R-induced phosphorylation of p47phox in PMN. In addition, in vitro stimulation of PMN with recombinant HMGB1 caused TLR4-dependent activation of NAD(P)H oxidase as well as increased ROS production through both MyD88-IRAK4-p38 MAPK and MyD88-IRAK4-Akt signaling pathways. Thus, PMN NAD(P)H oxidase activation, induced by HS/R and as mediated by HMGB1/TLR4 signaling, is an important mechanism responsible for PMN-mediated inflammation and organ injury after hemorrhage.

Original languageEnglish (US)
Pages (from-to)6573-6580
Number of pages8
JournalJournal of Immunology
Volume178
Issue number10
StatePublished - May 15 2007
Externally publishedYes

Fingerprint

Neutrophil Activation
Hemorrhagic Shock
NADPH Oxidase
Resuscitation
Reactive Oxygen Species
Inflammation
Phosphorylation
Inflammation Mediators
Inbred C3H Mouse
Wounds and Injuries
Alveolar Macrophages
p38 Mitogen-Activated Protein Kinases
Endotoxins
Reperfusion
Pneumonia
Neutrophils
Ischemia
Hemorrhage
Ligands
Lung

ASJC Scopus subject areas

  • Immunology

Cite this

Fan, J., Li, Y., Levy, R. M., Fan, J. J., Hackam, D., Vodovotz, Y., ... Wilson, M. A. (2007). Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils: Role of HMGB1-TLR4 signaling. Journal of Immunology, 178(10), 6573-6580.

Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils : Role of HMGB1-TLR4 signaling. / Fan, Jie; Li, Yuehua; Levy, Ryan M.; Fan, Janet J.; Hackam, David; Vodovotz, Yoram; Yang, Huan; Tracey, Kevin J.; Billiar, Timothy R.; Wilson, Mark A.

In: Journal of Immunology, Vol. 178, No. 10, 15.05.2007, p. 6573-6580.

Research output: Contribution to journalArticle

Fan, J, Li, Y, Levy, RM, Fan, JJ, Hackam, D, Vodovotz, Y, Yang, H, Tracey, KJ, Billiar, TR & Wilson, MA 2007, 'Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils: Role of HMGB1-TLR4 signaling', Journal of Immunology, vol. 178, no. 10, pp. 6573-6580.
Fan, Jie ; Li, Yuehua ; Levy, Ryan M. ; Fan, Janet J. ; Hackam, David ; Vodovotz, Yoram ; Yang, Huan ; Tracey, Kevin J. ; Billiar, Timothy R. ; Wilson, Mark A. / Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils : Role of HMGB1-TLR4 signaling. In: Journal of Immunology. 2007 ; Vol. 178, No. 10. pp. 6573-6580.
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abstract = "Hemorrhagic shock/resuscitation (HS/R)-induced generation of reactive oxygen species (ROS) plays an important role in posthemorrhage inflammation and tissue injury. We have recently reported that HS/R-activated neutrophils (PMN), through release of ROS, serve an important signaling function in mediating alveolar macrophage priming and lung inflammation. PMN NAD(P)H oxidase has been thought to be an important source of ROS following HS/R. TLR4 sits at the interface of microbial and sterile inflammation by mediating responses to both bacterial endotoxin and multiple endogenous ligands, including high-mobility group box 1 (HMGB1). Recent studies have implicated HMGB1 as an early mediator of inflammation after HS/R and organ ischemia/ reperfusion. In the present study, we tested the hypothesis that HS/R activates NAD(P)H oxidase in PMN through HMGB1/TLR4 signaling. We demonstrated that HS/R induced PMN NAD(P)H oxidase activation, in the form of phosphorylation of p47phox subunit of NAD(P)H oxidase, in wild-type mice; this induction was significantly diminished in TLR4-mutant C3H/HeJ mice. HMGB1 levels in lungs, liver, and serum were increased as early as 2 h after HS/R. Neutralizing Ab to HMGB1 prevented HS/R-induced phosphorylation of p47phox in PMN. In addition, in vitro stimulation of PMN with recombinant HMGB1 caused TLR4-dependent activation of NAD(P)H oxidase as well as increased ROS production through both MyD88-IRAK4-p38 MAPK and MyD88-IRAK4-Akt signaling pathways. Thus, PMN NAD(P)H oxidase activation, induced by HS/R and as mediated by HMGB1/TLR4 signaling, is an important mechanism responsible for PMN-mediated inflammation and organ injury after hemorrhage.",
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AU - Fan, Janet J.

AU - Hackam, David

AU - Vodovotz, Yoram

AU - Yang, Huan

AU - Tracey, Kevin J.

AU - Billiar, Timothy R.

AU - Wilson, Mark A.

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N2 - Hemorrhagic shock/resuscitation (HS/R)-induced generation of reactive oxygen species (ROS) plays an important role in posthemorrhage inflammation and tissue injury. We have recently reported that HS/R-activated neutrophils (PMN), through release of ROS, serve an important signaling function in mediating alveolar macrophage priming and lung inflammation. PMN NAD(P)H oxidase has been thought to be an important source of ROS following HS/R. TLR4 sits at the interface of microbial and sterile inflammation by mediating responses to both bacterial endotoxin and multiple endogenous ligands, including high-mobility group box 1 (HMGB1). Recent studies have implicated HMGB1 as an early mediator of inflammation after HS/R and organ ischemia/ reperfusion. In the present study, we tested the hypothesis that HS/R activates NAD(P)H oxidase in PMN through HMGB1/TLR4 signaling. We demonstrated that HS/R induced PMN NAD(P)H oxidase activation, in the form of phosphorylation of p47phox subunit of NAD(P)H oxidase, in wild-type mice; this induction was significantly diminished in TLR4-mutant C3H/HeJ mice. HMGB1 levels in lungs, liver, and serum were increased as early as 2 h after HS/R. Neutralizing Ab to HMGB1 prevented HS/R-induced phosphorylation of p47phox in PMN. In addition, in vitro stimulation of PMN with recombinant HMGB1 caused TLR4-dependent activation of NAD(P)H oxidase as well as increased ROS production through both MyD88-IRAK4-p38 MAPK and MyD88-IRAK4-Akt signaling pathways. Thus, PMN NAD(P)H oxidase activation, induced by HS/R and as mediated by HMGB1/TLR4 signaling, is an important mechanism responsible for PMN-mediated inflammation and organ injury after hemorrhage.

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