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XBP1 (X-Box-Binding Protein-1)-Dependent O-GlcNAcylation Is Neuroprotective in Ischemic Stroke in Young Mice and Its Impairment in Aged Mice Is Rescued by Thiamet-G.

Publication ,  Journal Article
Jiang, M; Yu, S; Yu, Z; Sheng, H; Li, Y; Liu, S; Warner, DS; Paschen, W; Yang, W
Published in: Stroke
June 2017

BACKGROUND AND PURPOSE: Impaired protein homeostasis induced by endoplasmic reticulum dysfunction is a key feature of a variety of age-related brain diseases including stroke. To restore endoplasmic reticulum function impaired by stress, the unfolded protein response is activated. A key unfolded protein response prosurvival pathway is controlled by the endoplasmic reticulum stress sensor (inositol-requiring enzyme-1), XBP1 (downstream X-box-binding protein-1), and O-GlcNAc (O-linked β-N-acetylglucosamine) modification of proteins (O-GlcNAcylation). Stroke impairs endoplasmic reticulum function, which activates unfolded protein response. The rationale of this study was to explore the potentials of the IRE1/XBP1/O-GlcNAc axis as a target for neuroprotection in ischemic stroke. METHODS: Mice with Xbp1 loss and gain of function in neurons were generated. Stroke was induced by transient or permanent occlusion of the middle cerebral artery in young and aged mice. Thiamet-G was used to increase O-GlcNAcylation. RESULTS: Deletion of Xbp1 worsened outcome after transient and permanent middle cerebral artery occlusion. After stroke, O-GlcNAcylation was activated in neurons of the stroke penumbra in young mice, which was largely Xbp1 dependent. This activation of O-GlcNAcylation was impaired in aged mice. Pharmacological increase of O-GlcNAcylation before or after stroke improved outcome in both young and aged mice. CONCLUSIONS: Our study indicates a critical role for the IRE1/XBP1 unfolded protein response branch in stroke outcome. O-GlcNAcylation is a prosurvival pathway that is activated in the stroke penumbra in young mice but impaired in aged mice. Boosting prosurvival pathways to counterbalance the age-related decline in the brain's self-healing capacity could be a promising strategy to improve ischemic stroke outcome in aged brains.

Duke Scholars

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Published In

Stroke

DOI

EISSN

1524-4628

Publication Date

June 2017

Volume

48

Issue

6

Start / End Page

1646 / 1654

Location

United States

Related Subject Headings

  • X-Box Binding Protein 1
  • Unfolded Protein Response
  • Thiazoles
  • Stroke
  • Pyrans
  • Protein Serine-Threonine Kinases
  • Protein Folding
  • Neuroprotection
  • Neurology & Neurosurgery
  • Mice, Transgenic
 

Citation

APA
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Jiang, M., Yu, S., Yu, Z., Sheng, H., Li, Y., Liu, S., … Yang, W. (2017). XBP1 (X-Box-Binding Protein-1)-Dependent O-GlcNAcylation Is Neuroprotective in Ischemic Stroke in Young Mice and Its Impairment in Aged Mice Is Rescued by Thiamet-G. Stroke, 48(6), 1646–1654. https://doi.org/10.1161/STROKEAHA.117.016579
Jiang, Meng, Shu Yu, Zhui Yu, Huaxin Sheng, Ying Li, Shuai Liu, David S. Warner, Wulf Paschen, and Wei Yang. “XBP1 (X-Box-Binding Protein-1)-Dependent O-GlcNAcylation Is Neuroprotective in Ischemic Stroke in Young Mice and Its Impairment in Aged Mice Is Rescued by Thiamet-G.Stroke 48, no. 6 (June 2017): 1646–54. https://doi.org/10.1161/STROKEAHA.117.016579.
Jiang, Meng, et al. “XBP1 (X-Box-Binding Protein-1)-Dependent O-GlcNAcylation Is Neuroprotective in Ischemic Stroke in Young Mice and Its Impairment in Aged Mice Is Rescued by Thiamet-G.Stroke, vol. 48, no. 6, June 2017, pp. 1646–54. Pubmed, doi:10.1161/STROKEAHA.117.016579.

Published In

Stroke

DOI

EISSN

1524-4628

Publication Date

June 2017

Volume

48

Issue

6

Start / End Page

1646 / 1654

Location

United States

Related Subject Headings

  • X-Box Binding Protein 1
  • Unfolded Protein Response
  • Thiazoles
  • Stroke
  • Pyrans
  • Protein Serine-Threonine Kinases
  • Protein Folding
  • Neuroprotection
  • Neurology & Neurosurgery
  • Mice, Transgenic