Featured Publications
Alcohol-induced Hsp90 acetylation is a novel driver of liver sinusoidal endothelial dysfunction and alcohol-related liver disease
Yang Y, Sangwung P, Kondo R, Jung Y, McConnell MJ, Jeong J, Utsumi T, Sessa WC, Iwakiri Y. Alcohol-induced Hsp90 acetylation is a novel driver of liver sinusoidal endothelial dysfunction and alcohol-related liver disease. Journal Of Hepatology 2021, 75: 377-386. PMID: 33675874, PMCID: PMC8292196, DOI: 10.1016/j.jhep.2021.02.028.Peer-Reviewed Original ResearchMeSH KeywordsAcetylationAdultAlcohol DrinkingAnalysis of VarianceAnimalsEndothelial CellsHSP90 Heat-Shock ProteinsHumansLiver Diseases, AlcoholicMiceRatsConceptsEndothelial nitric oxide synthaseAlcohol-induced liver injuryLiver sinusoidal endothelial cellsAlcohol-related liver diseaseLiver injuryLSEC dysfunctionHsp90 acetylationNO productionHistone deacetylase 6Liver diseaseTherapeutic strategiesHeat shock protein 90 (Hsp90) acetylationLiver sinusoidal endothelial dysfunctionSinusoidal endothelial cell dysfunctionMouse liver sinusoidal endothelial cellsEndothelial cell dysfunctionNitric oxide synthaseEthanol-fed miceSinusoidal endothelial dysfunctionPotential therapeutic approachPotential therapeutic strategyNitric oxide productionNew therapeutic strategiesSinusoidal endothelial cellsAcetylation of Hsp90
2020
The lymphatic system in alcohol-associated liver disease
Kondo R, Iwakiri Y. The lymphatic system in alcohol-associated liver disease. Clinical And Molecular Hepatology 2020, 26: 633-638. PMID: 32951411, PMCID: PMC7641555, DOI: 10.3350/cmh.2020.0179.BooksConceptsAlcoholic liver diseaseLymphatic systemLiver diseaseTreatment of ALDAlcohol-associated liver diseaseAlcohol-related diseasesEffects of alcoholHepatic lymphaticsFluid balanceCell surveillanceTherapeutic potentialImmune cell surveillanceDiseaseInterstitial fluid balanceReview articlePathogenesisLymphatics
2017
An endoplasmic reticulum protein, Nogo‐B, facilitates alcoholic liver disease through regulation of kupffer cell polarization
Park J, Shao M, Kim MY, Baik SK, Cho MY, Utsumi T, Satoh A, Ouyang X, Chung C, Iwakiri Y. An endoplasmic reticulum protein, Nogo‐B, facilitates alcoholic liver disease through regulation of kupffer cell polarization. Hepatology 2017, 65: 1720-1734. PMID: 28090670, PMCID: PMC5397326, DOI: 10.1002/hep.29051.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsEndoplasmic Reticulum StressHumansKupffer CellsLiver Diseases, AlcoholicMaleMice, Inbred C57BLMice, KnockoutNogo ProteinsConceptsAlcoholic liver diseasePositive Kupffer cellsKupffer cellsLiver injuryALD patientsLiver diseaseM1 polarizationKO miceM2 polarizationLieber-DeCarli ethanol liquid dietDisease severityM1/M2 polarizationKupffer cell polarizationEthanol liquid dietHepatic triglyceride levelsM2 macrophage polarizationHigher hepatic triglyceride levelsChronic ethanol feedingNew therapeutic targetsER stressAbsence of NogoM2 statusWT miceM1 activationTriglyceride levels