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N-glycanase NGLY1 regulates mitochondrial homeostasis and inflammation through NRF1.

Abstract
Mutations in the NGLY1 (N-glycanase 1) gene, encoding an evolutionarily conserved deglycosylation enzyme, are associated with a rare congenital disorder leading to global developmental delay and neurological abnormalities. The molecular mechanism of the NGLY1 disease and its function in tissue and immune homeostasis remain unknown. Here, we find that NGLY1-deficient human and mouse cells chronically activate cytosolic nucleic acid-sensing pathways, leading to elevated interferon gene signature. We also find that cellular clearance of damaged mitochondria by mitophagy is impaired in the absence of NGLY1, resulting in severely fragmented mitochondria and activation of cGAS-STING as well as MDA5-MAVS pathways. Furthermore, we show that NGLY1 regulates mitochondrial homeostasis through transcriptional factor NRF1. Remarkably, pharmacological activation of a homologous but nonglycosylated transcriptional factor NRF2 restores mitochondrial homeostasis and suppresses immune gene activation in NGLY1-deficient cells. Together, our findings reveal novel functions of the NGLY1-NRF1 pathway in mitochondrial homeostasis and inflammation and uncover an unexpected therapeutic strategy using pharmacological activators of NRF2 for treating mitochondrial and immune dysregulation.
AuthorsKun Yang, Ryan Huang, Haruhiko Fujihira, Tadashi Suzuki, Nan Yan
JournalThe Journal of experimental medicine (J Exp Med) Vol. 215 Issue 10 Pg. 2600-2616 (10 01 2018) ISSN: 1540-9538 [Electronic] United States
PMID30135079 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2018 Yang et al.
Chemical References
  • NF-E2-Related Factor 1
  • NF-E2-Related Factor 2
  • Nfe2L1 protein, mouse
  • Nfe2l2 protein, mouse
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
Topics
  • Animals
  • Congenital Disorders of Glycosylation (genetics, immunology, pathology)
  • Homeostasis (genetics, immunology)
  • Humans
  • Inflammation (genetics, immunology, pathology)
  • Mice
  • Mice, Knockout
  • Mitochondria (genetics, immunology, pathology)
  • NF-E2-Related Factor 1 (genetics, immunology)
  • NF-E2-Related Factor 2 (genetics, immunology)
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase (deficiency, genetics, immunology)

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