XBP1 mitigates aminoglycoside-induced endoplasmic reticulum stress and neuronal cell death

Cell Death Dis. 2015 May 14;6(5):e1763. doi: 10.1038/cddis.2015.108.

Abstract

Here we study links between aminoglycoside-induced mistranslation, protein misfolding and neuropathy. We demonstrate that aminoglycosides induce misreading in mammalian cells and assess endoplasmic reticulum (ER) stress and unfolded protein response (UPR) pathways. Genome-wide transcriptome and proteome analyses revealed upregulation of genes related to protein folding and degradation. Quantitative PCR confirmed induction of UPR markers including C/EBP homologous protein, glucose-regulated protein 94, binding immunoglobulin protein and X-box binding protein-1 (XBP1) mRNA splicing, which is crucial for UPR activation. We studied the effect of a compromised UPR on aminoglycoside ototoxicity in haploinsufficient XBP1 (XBP1(+/-)) mice. Intra-tympanic aminoglycoside treatment caused high-frequency hearing loss in XBP1(+/-) mice but not in wild-type littermates. Densities of spiral ganglion cells and synaptic ribbons were decreased in gentamicin-treated XBP1(+/-) mice, while sensory cells were preserved. Co-injection of the chemical chaperone tauroursodeoxycholic acid attenuated hearing loss. These results suggest that aminoglycoside-induced ER stress and cell death in spiral ganglion neurons is mitigated by XBP1, masking aminoglycoside neurotoxicity at the organismal level.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Cell Line
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Endoplasmic Reticulum / pathology
  • Endoplasmic Reticulum Stress / drug effects*
  • Female
  • Gentamicins / pharmacology*
  • HEK293 Cells
  • Hair Cells, Auditory / pathology
  • Hearing Loss, High-Frequency* / chemically induced
  • Hearing Loss, High-Frequency* / genetics
  • Hearing Loss, High-Frequency* / pathology
  • Humans
  • Male
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred CBA
  • Neurons / pathology
  • Protein Biosynthesis / drug effects
  • Protein Folding
  • Proteostasis Deficiencies
  • RNA Splicing / genetics
  • Regulatory Factor X Transcription Factors
  • Spiral Ganglion / cytology
  • Spiral Ganglion / drug effects
  • Spiral Ganglion / pathology
  • Taurochenodeoxycholic Acid / pharmacology*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Unfolded Protein Response / genetics
  • Unfolded Protein Response / physiology
  • X-Box Binding Protein 1

Substances

  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, human
  • DNA-Binding Proteins
  • Gentamicins
  • Membrane Glycoproteins
  • Regulatory Factor X Transcription Factors
  • Transcription Factors
  • X-Box Binding Protein 1
  • XBP1 protein, human
  • Xbp1 protein, mouse
  • endoplasmin
  • Taurochenodeoxycholic Acid
  • ursodoxicoltaurine

Associated data

  • GEO/GSE57198