Induction of Apoptosis Coupled to Endoplasmic Reticulum Stress through Regulation of CHOP and JNK in Bone Marrow Mesenchymal Stem Cells from Patients with Systemic Lupus Erythematosus

J Immunol Res. 2015:2015:183738. doi: 10.1155/2015/183738. Epub 2015 May 19.

Abstract

Previous studies indicated that bone marrow mesenchymal stem cells (BM-MSCs) from patients with systemic lupus erythematosus (SLE) exhibited the phenomenon of apoptosis. In this study, we aimed to investigate whether apoptosis of BM-MSCs from SLE patients were dysregulated. In this paper, endoplasmic reticulum stress (ERS) was evidenced by increased expression of phosphorylated protein kinase RNA-like ER kinase (PERK) and inositol-requiring protein-1 (IRE-1). We also found the activation of downstream target eukaryotic translation initiator factor 2α (eIF 2α) and CCAAT/enhancer-binding protein- (C/EBP-) homologous protein (CHOP) in BM-MSCs from SLE patients. Interestingly, we discovered that 4-phenylbutyric acid (4-PBA), a selective inhibitor of ERS, blocked the apoptosis of BM-MSCs from SLE patients and alleviated the level of Jun N-terminal kinase1/2 (JNK1/2) and CHOP. Furthermore, blockage of PERK signaling expression by siRNA not only significantly reduced the expression of CHOP, but also activated the anti-apoptotic regulator B-cell lymphoma-2 (Bcl-2). Blockage of IRE-1 or JNK1/2 by siRNA resulted in the decreased expression of JNK1/2 and proapoptosis protein Bcl-2 associated protein X (BAX). These results implicated that ERS-mediated apoptosis was a critical determinant of BM-MSCs from SLE patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Apoptosis / physiology*
  • Bone Marrow Cells / metabolism*
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Case-Control Studies
  • Endoplasmic Reticulum Stress / physiology*
  • Endoribonucleases / metabolism
  • Eukaryotic Initiation Factor-2 / metabolism
  • Female
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Lupus Erythematosus, Systemic / metabolism*
  • Mesenchymal Stem Cells / metabolism*
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / physiology
  • Transcription Factor CHOP / metabolism*
  • Young Adult
  • bcl-2-Associated X Protein / metabolism
  • eIF-2 Kinase / metabolism

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DDIT3 protein, human
  • Eukaryotic Initiation Factor-2
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Transcription Factor CHOP
  • EIF2AK3 protein, human
  • ERN1 protein, human
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase
  • JNK Mitogen-Activated Protein Kinases
  • Endoribonucleases