PRELI is a mitochondrial regulator of human primary T-helper cell apoptosis, STAT6, and Th2-cell differentiation

Blood. 2009 Feb 5;113(6):1268-77. doi: 10.1182/blood-2008-07-166553. Epub 2008 Oct 22.

Abstract

The identification of novel factors regulating human T helper (Th)-cell differentiation into functionally distinct Th1 and Th2 subsets is important for understanding the mechanisms behind human autoimmune and allergic diseases. We have identified a protein of relevant evolutionary and lymphoid interest (PRELI), a novel protein that induces oxidative stress and a mitochondrial apoptosis pathway in human primary Th cells. We also demonstrated that PRELI inhibits Th2-cell development and down-regulates signal transducer and activator of transcription 6 (STAT6), a key transcription factor driving Th2 differentiation. Our data suggest that calpain, an oxidative stress-induced cysteine protease, is involved in the PRELI-induced down-regulation of STAT6. Moreover, we observed that a strong T-cell receptor (TCR) stimulus induces expression of PRELI and inhibits Th2 development. Our results suggest that PRELI is involved in a mechanism wherein the strength of the TCR stimulus influences the polarization of Th cells. This study identifies PRELI as a novel factor influencing the human primary Th-cell death and differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology*
  • Blotting, Western
  • Calpain / metabolism
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Cytokines / metabolism
  • Fetal Blood / cytology
  • Fluorescent Antibody Technique
  • Gene Expression Profiling
  • Humans
  • Infant, Newborn
  • Kidney / cytology
  • Kidney / metabolism
  • Lymphocyte Activation
  • Membrane Potential, Mitochondrial
  • Mitochondria / metabolism*
  • Mitochondrial Proteins
  • Oligonucleotide Array Sequence Analysis
  • Oxidative Stress
  • Proteins / physiology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Receptors, Antigen, T-Cell / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / metabolism*
  • Signal Transduction
  • Th1 Cells / physiology*
  • Th2 Cells / immunology

Substances

  • Cytokines
  • Mitochondrial Proteins
  • PRELID1 protein, human
  • Proteins
  • RNA, Messenger
  • Reactive Oxygen Species
  • Receptors, Antigen, T-Cell
  • STAT6 Transcription Factor
  • STAT6 protein, human
  • Calpain