Increased apoptosis after autoimmune regulator expression in epithelial cells revealed by a combined quantitative proteomics approach

J Proteome Res. 2010 May 7;9(5):2600-9. doi: 10.1021/pr100044d.

Abstract

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare autosomal recessive autoimmune disease, affecting many endocrine tissues. APECED is associated to the lack of function of a single gene called AutoImmune REgulator (AIRE). Aire knockout mice develop various autoimmune disorders affecting different organs, indicating that Aire is a key gene in the control of organ-specific autoimmune diseases. AIRE is mainly expressed by medullary thymic epithelial cells (mTECs), and its absence results in the loss of tolerance against tissue restricted antigens (TRAs). Aire induces the transcription of genes encoding for TRAs in mTECs. In this report, the analysis of AIRE's effect on the cellular proteome was approached by the combination of two quantitative proteomics techniques, 2D-DIGE and ICPL, using an AIRE-transfected and nontransfected epithelial cell line. The results showed increased levels of several chaperones, (HSC70, HSP27 and tubulin-specific chaperone A) in AIRE-expressing cells, while various cytoskeleton interacting proteins, that is, transgelin, caldesmon, tropomyosin alpha-1 chain, myosin regulatory light polypeptide 9, and myosin-9, were decreased. Furthermore, some apoptosis-related proteins were differentially expressed. Data were confirmed by Western blot and flow cytometry analysis. Apoptosis assays with annexin V and etoposide demonstrated that AIRE-positive cells suffer more spontaneous apoptosis and are less resistant to apoptosis induction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Apoptosis / physiology*
  • Calmodulin-Binding Proteins / analysis
  • Cell Line, Tumor
  • Electrophoresis, Gel, Two-Dimensional
  • Epithelial Cells / metabolism*
  • Flow Cytometry
  • HSP70 Heat-Shock Proteins / analysis
  • Humans
  • Isotope Labeling
  • Proteome / analysis*
  • Proteomics / methods*
  • Reproducibility of Results
  • Signal Transduction
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Calmodulin-Binding Proteins
  • HSP70 Heat-Shock Proteins
  • Proteome
  • Transcription Factors