The protective role of pregnane X receptor in lipopolysaccharide/D- galactosamine-induced acute liver injury

Kun Wang, Ivan Damjanov, Yu-Jui Yvonne Wan

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

The pregnane X receptor (PXR) is a nuclear receptor transcription factor regulating drug-metabolizing enzymes and transporters that facilitate xenobiotic and endobiotic detoxification. Recent studies show that PXR is important in abrogating intestinal tissue damage. This study examines the role of PXR in lipopolysaccharide (LPS)/D-galactosamine (GalN)-induced acute liver injury using wild-type and PXR-null mice. LPS/GalN-treated PXR-null mice had greater increases of alanine transaminase (ALT), hepatocyte apoptosis, necrosis, and hemorrhagic liver injury than wild-type mice. LPS/GalN-mediated phosphorylation of JNK1/2 and ERK1/2 was differentially regulated in wild-type and PXR-null mice. Importantly, LPS/GalN-induced hepatic Stat3 survival signaling was impaired and early activation of Jak2 was delayed in PXR-null mice. Expression levels of pro-survival proteins Bcl-xL and heme oxygenase-1 (HO-1), which are downstream of Stat3, were substantially lower in PXR-null than wild-type mouse livers after LPS/GalN treatment. Autophagy is also involved in LPS/GalN-induced liver injury. Lack of PXR resulted in a significant reduction of LC3B-I,-II as well as Beclin-1 protein levels after LPS/GalN treatment. In addition, PXR is implicated in hepatocytes homeostasis. Taken together, PXR is a critical hepatoprotective factor. Increases of LPS/GalN-induced hepatocyte apoptosis and liver injury in PXR-null mice are due to deregulated mitogen-activated protein (MAP) kinase activation as well as delayed Jak2/Stat3 activation, which lead to a compromise in defense mechanisms that involve Bcl-xL-, HO-1, and autophagy-mediated pathways.

Original languageEnglish (US)
Pages (from-to)257-265
Number of pages9
JournalLaboratory Investigation
Volume90
Issue number2
DOIs
StatePublished - Feb 2010
Externally publishedYes

Fingerprint

Galactosamine
Lipopolysaccharides
Liver
Wounds and Injuries
Hepatocytes
Heme Oxygenase-1
Autophagy
pregnane X receptor
Apoptosis
Xenobiotics
Cytoplasmic and Nuclear Receptors
Mitogen-Activated Protein Kinases
Alanine Transaminase
Homeostasis
Transcription Factors
Necrosis

Keywords

  • Apoptosis
  • Jak2/Stat3
  • Liver injury
  • MAP kinases
  • PXR

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Cell Biology
  • Molecular Biology

Cite this

The protective role of pregnane X receptor in lipopolysaccharide/D- galactosamine-induced acute liver injury. / Wang, Kun; Damjanov, Ivan; Wan, Yu-Jui Yvonne.

In: Laboratory Investigation, Vol. 90, No. 2, 02.2010, p. 257-265.

Research output: Contribution to journalArticle

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