Modification of nuclear PML protein by SUMO-1 regulates Fas-induced apoptosis in rheumatoid arthritis synovial fibroblasts

Proc Natl Acad Sci U S A. 2007 Mar 20;104(12):5073-8. doi: 10.1073/pnas.0608773104. Epub 2007 Mar 14.

Abstract

The small ubiquitin-like modifier (SUMO)-1 is an important posttranslational regulator of different signaling pathways and involved in the formation of promyelocytic leukemia (PML) protein nuclear bodies (NBs). Overexpression of SUMO-1 has been associated with alterations in apoptosis, but the underlying mechanisms and their relevance for human diseases are not clear. Here, we show that the increased expression of SUMO-1 in rheumatoid arthritis (RA) synovial fibroblasts (SFs) contributes to the resistance of these cells against Fas-induced apoptosis through increased SUMOylation of nuclear PML protein and increased recruitment of the transcriptional repressor DAXX to PML NBs. We also show that the nuclear SUMO-protease SENP1, which is found at lower levels in RA SFs, can revert the apoptosis-inhibiting effects of SUMO-1 by releasing DAXX from PML NBs. Our findings indicate that in RA SFs overexpression of SENP1 can alter the SUMO-1-mediated recruitment of DAXX to PML NBs, thus influencing the proapoptotic effects of DAXX. Accumulation of DAXX in PML NBs by SUMO-1 may, therefore, contribute to the pathogenesis of inflammatory disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Apoptosis / drug effects*
  • Arthritis, Rheumatoid / pathology*
  • Cell Nucleus / drug effects
  • Cell Nucleus / enzymology
  • Cell Nucleus / metabolism*
  • Co-Repressor Proteins
  • Cysteine Endopeptidases
  • Endopeptidases / genetics
  • Endopeptidases / metabolism
  • Fas Ligand Protein / pharmacology*
  • Fibroblasts / drug effects
  • Fibroblasts / pathology*
  • Gene Expression / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Intranuclear Inclusion Bodies / drug effects
  • Molecular Chaperones
  • Neoplasm Proteins / metabolism*
  • Nuclear Proteins / metabolism*
  • Promyelocytic Leukemia Protein
  • Protein Processing, Post-Translational / drug effects
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • SUMO-1 Protein / metabolism*
  • Synovial Fluid / cytology
  • Synovial Fluid / drug effects
  • Transcription Factors / metabolism*
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Co-Repressor Proteins
  • DAXX protein, human
  • Fas Ligand Protein
  • Molecular Chaperones
  • Neoplasm Proteins
  • Nuclear Proteins
  • Promyelocytic Leukemia Protein
  • RNA, Messenger
  • SUMO-1 Protein
  • Transcription Factors
  • Tumor Suppressor Proteins
  • PML protein, human
  • Endopeptidases
  • SENP1 protein, human
  • Cysteine Endopeptidases