PUBLICATION
Impaired redox and protein homeostasis as risk factors and therapeutic targets in toxin-induced biliary atresia
- Authors
- Zhao, X., Lorent, K., Escobar-Zarate, D., Rajagopalan, R., Loomes, K.M., Gillespie, K., Mesaros, C., Estrada, M.A., Blair, I., Winkler, J.D., Spinner, N.B., Devoto, M., Pack, M.
- ID
- ZDB-PUB-200609-1
- Date
- 2020
- Source
- Gastroenterology 159(3): 1068-1084.e2 (Journal)
- Registered Authors
- Pack, Michael
- Keywords
- Chronic Liver Disease, cholestasis, glutathione metabolism
- MeSH Terms
-
- Acetylcysteine/pharmacology
- Acetylcysteine/therapeutic use
- Animals
- Animals, Genetically Modified
- Benzodioxoles/toxicity
- Bile Ducts/cytology
- Bile Ducts/drug effects
- Bile Ducts/pathology*
- Biliary Atresia/chemically induced
- Biliary Atresia/drug therapy*
- Biliary Atresia/genetics
- Biliary Atresia/pathology
- Cell Line
- Cyclic GMP/agonists
- Cyclic GMP/metabolism
- Disease Models, Animal
- Drug Evaluation, Preclinical
- Drug Therapy, Combination
- Free Radical Scavengers/pharmacology*
- Free Radical Scavengers/therapeutic use
- Glutathione/metabolism
- Humans
- Oxidation-Reduction/drug effects*
- Proteostasis/drug effects*
- Proteostasis/genetics
- Signal Transduction/drug effects
- Zebrafish
- PubMed
- 32505743 Full text @ Gastroenterology
Citation
Zhao, X., Lorent, K., Escobar-Zarate, D., Rajagopalan, R., Loomes, K.M., Gillespie, K., Mesaros, C., Estrada, M.A., Blair, I., Winkler, J.D., Spinner, N.B., Devoto, M., Pack, M. (2020) Impaired redox and protein homeostasis as risk factors and therapeutic targets in toxin-induced biliary atresia. Gastroenterology. 159(3):1068-1084.e2.
Abstract
Background and aims Extra-hepatic biliary atresia (BA) is a pediatric liver disease with no approved medical therapy. Recent studies using human samples and experimental modeling suggest that glutathione redox metabolism and heterogeneity play a role in disease pathogenesis. We sought to dissect the mechanistic basis of liver redox variation and explore how other stress responses affect cholangiocyte injury in BA.
Methods We performed quantitative in situ hepatic glutathione redox mapping in zebrafish larvae carrying targeted mutations in glutathione metabolism genes and correlated these findings with sensitivity to the plant-derived BA-linked toxin biliatresone. We also determined whether genetic disruption of HSP90 protein quality control pathway genes implicated in human BA altered biliatresone toxicity in zebrafish and human cholangiocytes. An in vivo screen of a known drug library was performed to identify novel modifiers of cholangiocyte injury in the zebrafish experimental BA model with subsequent validation.
Results Glutathione metabolism gene mutations caused regionally distinct changes in the redox potential of cholangiocytes that differentially sensitized them to biliatresone. Disruption of human BA-implicated HSP90 pathway genes sensitized zebrafish and human cholangiocytes to biliatresone-induced injury independent of glutathione. Phosphodiesterase-5 inhibitors (PDE5i) and other cGMP signaling activators worked synergistically with the glutathione precursor N-acetylcysteine (NAC) in preventing biliatresone-induced injury in zebrafish and human cholangiocytes. PDE5i enhanced proteasomal degradation and required intact HSP90 chaperone.
Conclusion Regional variation in glutathione metabolism underlies sensitivity to the biliary toxin biliatresone, and may account for the reported association between BA transplant-free survival and glutathione metabolism gene expression. Human BA can be causatively linked to genetic modulation of protein quality control. Combined treatment with NAC and cGMP signaling enhancers warrants further investigation as therapy for BA.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping