Antioxidants reduce endoplasmic reticulum stress and improve protein secretion
University of Michigan · Pediatrics and Genetics · +1 more institution
Abstract
Protein misfolding in the endoplasmic reticulum (ER) contributes to the pathogenesis of many diseases. Although oxidative stress can disrupt protein folding, how protein misfolding and oxidative stress impact each other has not been explored. We have analyzed expression of coagulation factor VIII (FVIII), the protein deficient in hemophilia A, to elucidate the relationship between protein misfolding and oxidative stress. Newly synthesized FVIII misfolds in the ER lumen, activates the unfolded protein response (UPR), causes oxidative stress, and induces apoptosis in vitro and in vivo in mice. Strikingly, antioxidant treatment reduces UPR activation, oxidative stress, and apoptosis, and increases FVIII secretion…
Citation impact
- FWCI
- 17.42
- Percentile
- 100%
- References
- 54
Authors
7Topics & keywords
- Unfolded protein response
- Endoplasmic reticulum
- Oxidative stress
- Reactive oxygen species
- Cell biology
- Protein folding
- Secretion
- Chemistry