17β-Estradiol downregulates Kupffer cell TLR4-dependent p38 MAPK pathway and normalizes inflammatory cytokine production following trauma-hemorrhage

Ya Ching Hsieh, Michael Frink, Bjoern M. Thobe, Jun Te Hsu, Mashkoor A. Choudhry, Martin G Schwacha, Kirby I. Bland, Irshad H. Chaudry

Research output: Contribution to journalArticle

49 Citations (Scopus)

Abstract

Although studies have shown that 17β-estradiol (estradiol) normalized Kupffer cell function following trauma-hemorrhage, the mechanism by which E2 maintains immune function remains unclear. Activation of Toll-like receptor 4 (TLR4) initiates an inflammatory cascade, involving activation of p38 mitogen-activated protein kinase (MAPK), phosphatidylinositol 3-kinase (PI3K), and nuclear factor-κB (NF-κB). This leads to the release of proinflammatory cytokines. Thus, we hypothesized that the salutary effects of estradiol on Kupffer cell function following trauma-hemorrhage are mediated via negative regulation of TLR4-dependent p38 MAPK and NF-κB. TLR4 mutant (C3H/HeJ) and wild type (C3H/HeOuJ) mice were subjected to trauma-hemorrhage (mean BP 35 ± 5 mmHg ∼90 min, then resuscitation) or sham operation. Administration of estradiol following trauma-hemorrhage in wild type mice decreased Kupffer cell TLR4 expression as well as prevented the phosphorylation of p38 MAPK and NF-κB. This was accompanied by normalization of Kupffer cell production capacities of IL-6, TNF-α, macrophage inflammatory protein (MIP)-1α, and MIP-2 and the decrease in plasma cytokine levels. In contrast, TLR4 mutant mice did not exhibit the increase in Kupffer cell p38 MAPK and NF-κB activation, cytokine production, or the increase in circulating cytokine levels following trauma-hemorrhage. No difference was observed in activation of PI3K among groups. These results suggest that the protective effect of estradiol on Kupffer cell function is mediated via downregulation of TLR4-dependent p38 MAPK and NF-κB signaling following trauma-hemorrhage, which prevents the systemic release of cytokines.

Original languageEnglish (US)
Pages (from-to)2165-2172
Number of pages8
JournalMolecular Immunology
Volume44
Issue number9
DOIs
StatePublished - Mar 2007
Externally publishedYes

Fingerprint

Toll-Like Receptor 4
Kupffer Cells
p38 Mitogen-Activated Protein Kinases
Estradiol
Down-Regulation
Hemorrhage
Cytokines
Wounds and Injuries
Phosphatidylinositol 3-Kinase
Proto-Oncogene Proteins c-akt
Chemokine CXCL2
Macrophage Inflammatory Proteins
Inbred C3H Mouse
Resuscitation
Interleukin-6
Phosphorylation

Keywords

  • Estrogen
  • Hemorrhagic shock
  • MIP-1α
  • MIP-2
  • NF-κB

ASJC Scopus subject areas

  • Molecular Biology
  • Immunology

Cite this

17β-Estradiol downregulates Kupffer cell TLR4-dependent p38 MAPK pathway and normalizes inflammatory cytokine production following trauma-hemorrhage. / Hsieh, Ya Ching; Frink, Michael; Thobe, Bjoern M.; Hsu, Jun Te; Choudhry, Mashkoor A.; Schwacha, Martin G; Bland, Kirby I.; Chaudry, Irshad H.

In: Molecular Immunology, Vol. 44, No. 9, 03.2007, p. 2165-2172.

Research output: Contribution to journalArticle

Hsieh, Ya Ching ; Frink, Michael ; Thobe, Bjoern M. ; Hsu, Jun Te ; Choudhry, Mashkoor A. ; Schwacha, Martin G ; Bland, Kirby I. ; Chaudry, Irshad H. / 17β-Estradiol downregulates Kupffer cell TLR4-dependent p38 MAPK pathway and normalizes inflammatory cytokine production following trauma-hemorrhage. In: Molecular Immunology. 2007 ; Vol. 44, No. 9. pp. 2165-2172.
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abstract = "Although studies have shown that 17β-estradiol (estradiol) normalized Kupffer cell function following trauma-hemorrhage, the mechanism by which E2 maintains immune function remains unclear. Activation of Toll-like receptor 4 (TLR4) initiates an inflammatory cascade, involving activation of p38 mitogen-activated protein kinase (MAPK), phosphatidylinositol 3-kinase (PI3K), and nuclear factor-κB (NF-κB). This leads to the release of proinflammatory cytokines. Thus, we hypothesized that the salutary effects of estradiol on Kupffer cell function following trauma-hemorrhage are mediated via negative regulation of TLR4-dependent p38 MAPK and NF-κB. TLR4 mutant (C3H/HeJ) and wild type (C3H/HeOuJ) mice were subjected to trauma-hemorrhage (mean BP 35 ± 5 mmHg ∼90 min, then resuscitation) or sham operation. Administration of estradiol following trauma-hemorrhage in wild type mice decreased Kupffer cell TLR4 expression as well as prevented the phosphorylation of p38 MAPK and NF-κB. This was accompanied by normalization of Kupffer cell production capacities of IL-6, TNF-α, macrophage inflammatory protein (MIP)-1α, and MIP-2 and the decrease in plasma cytokine levels. In contrast, TLR4 mutant mice did not exhibit the increase in Kupffer cell p38 MAPK and NF-κB activation, cytokine production, or the increase in circulating cytokine levels following trauma-hemorrhage. No difference was observed in activation of PI3K among groups. These results suggest that the protective effect of estradiol on Kupffer cell function is mediated via downregulation of TLR4-dependent p38 MAPK and NF-κB signaling following trauma-hemorrhage, which prevents the systemic release of cytokines.",
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AU - Thobe, Bjoern M.

AU - Hsu, Jun Te

AU - Choudhry, Mashkoor A.

AU - Schwacha, Martin G

AU - Bland, Kirby I.

AU - Chaudry, Irshad H.

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