Peroxisome proliferator-activated receptor γ-induced T cell apoptosis reduces survival during polymicrobial sepsis

Am J Respir Crit Care Med. 2011 Jul 1;184(1):64-74. doi: 10.1164/rccm.201010-1585OC. Epub 2011 Feb 25.

Abstract

Rationale: Despite intensive research, sepsis displays the most prevalent cause of death on intensive care units. The hallmark of sepsis is an overshooting T-cell death that reduces host defense mechanisms and that is associated with poor patient survival. Previous in vitro studies revealed that the expression of the transcription factor peroxisome proliferator-activated receptor (PPAR) γ was increased in isolated T cells of patients with sepsis.

Objectives: We determined the importance of targeting PPARγ for sepsis treatment and underlying molecular mechanisms for T-cell apoptosis in vivo.

Methods: To mimic human systemic inflammation and septic conditions, we used a nonlethal endotoxemia and a lethal cecum ligation and puncture polymicrobial sepsis model.

Measurements and main results: PPARγ inhibition in T cells with either the PPARγ antagonist GW9662 or a newly generated T cell-specific PPARγ knockout (Tc-PPARγ(-/-)) mice provided a survival advantage during polymicrobial sepsis in mice, which correlated with abrogated T-cell depletion in both in vivo models. Pathway analysis revealed increased antiapoptotic IL-2 and Bcl-2 expression, and activated prosurvival PI3K/Akt signaling under PPARγ-deficient conditions. In line, neutralizing IL-2 in Tc-PPARγ(-/-) mice resulted in T-cell apoptosis and increased mortality.

Conclusions: Our results provide evidence for a pivotal involvement of PPARγ in T-cell depletion by activating two important apoptosis pathways, and subsequently provoking the breakdown of defense mechanisms during systemic inflammation and sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anilides / pharmacology
  • Animals
  • Apoptosis*
  • Interleukin-2 / metabolism
  • Mice
  • Mice, Knockout
  • NFATC Transcription Factors / metabolism
  • PPAR gamma / antagonists & inhibitors
  • PPAR gamma / physiology*
  • PTEN Phosphohydrolase / metabolism
  • Peritonitis / immunology
  • Peritonitis / microbiology
  • Peritonitis / physiopathology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Sepsis / immunology
  • Sepsis / microbiology
  • Sepsis / mortality*
  • Sepsis / physiopathology
  • Signal Transduction
  • Survival Rate
  • T-Lymphocytes / physiology*

Substances

  • 2-chloro-5-nitrobenzanilide
  • Anilides
  • Interleukin-2
  • NFATC Transcription Factors
  • PPAR gamma
  • Proto-Oncogene Proteins c-bcl-2
  • Phosphatidylinositol 3-Kinases
  • PTEN Phosphohydrolase
  • PTEN protein, human