Prolyl isomerase pin1 protects mice from endotoxin shock

PLoS One. 2011 Feb 4;6(2):e14656. doi: 10.1371/journal.pone.0014656.

Abstract

Background: Prolyl isomerase Pin1 may be involved in innate immunity against microbial infection, but the mechanism how Pin1 controls the innate immunity is poorly understood.

Methodology/principal findings: Injection of lipopolysaccharide (LPS) into the mice induces inflammatory pulmonary disorder and sometimes the serious damages lead to death. Comparing to the wild-type (WT) mice, the Pin1⁻/⁻ mice showed more serious damages in lung and the lower survival rate after the LPS injection. We compared the levels of typical inflammatory cytokines. Pin1⁻/⁻ mice overreacted to the LPS injection to produce inflammatory cytokines, especially IL-6 more than WT mice. We showed that Pin1 binds phosphorylated PU.1 and they localize together in a nucleus. These results suggest that Pin1 controls the transcriptional activity of PU.1 and suppresses overreaction of macrophage that causes serious damages in lung.

Conclusions/significance: Pin1 may protect the mice from serious inflammation by LPS injection by attenuating the increase of IL-6 transcription of the mouse macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Infections / complications
  • Bacterial Infections / genetics
  • COS Cells
  • Cells, Cultured
  • Chlorocebus aethiops
  • Dose-Response Relationship, Drug
  • Endotoxins / adverse effects
  • Inflammation / chemically induced
  • Inflammation / genetics
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Interleukin-6 / physiology
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Knockout
  • Multiple Organ Failure / chemically induced
  • Multiple Organ Failure / genetics
  • Multiple Organ Failure / mortality
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Peptidylprolyl Isomerase / genetics
  • Peptidylprolyl Isomerase / metabolism
  • Peptidylprolyl Isomerase / physiology*
  • Proto-Oncogene Proteins / metabolism
  • Shock, Septic / etiology
  • Shock, Septic / genetics
  • Shock, Septic / prevention & control*
  • Trans-Activators / metabolism

Substances

  • Endotoxins
  • Interleukin-6
  • Lipopolysaccharides
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Proto-Oncogene Proteins
  • Trans-Activators
  • proto-oncogene protein Spi-1
  • Peptidylprolyl Isomerase
  • Pin1 protein, mouse