Published February 28, 2014 | Version v1
Journal article

Exploring the effects of tert-butylhydroperoxide induced liver injury using proteomic approach

  • 1. Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taiwan (China)
  • 2. Department of Hepato-Gastroenterology, Chang Gung Memorial Hospital, Chiayi, Taiwan (China)
  • 3. Chang Gung University College of Medicine, Taoyuan, Taiwan (China)
  • 4. Division of Colon and Rectal Surgery, Department of Surgery, Chang Gung Memorial Hospital, Chiayi, Taiwan (China)
  • 5. Department of Surgery, Chang Gung Memorial Hospital – Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, Taiwan (China)
  • 6. Department of Colorectal Surgery, Chang Gung Memorial Hospital – Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, Taiwan (China)
  • 7. Research Center for Industry of Human Ecology, Chang Gung University of Science and Technology, Taoyuan, Taiwan (China)
  • 8. Chronic Diseases and Health Promotion Research Center, CGUST, Taiwan (China)
  • 9. Department of Nursing, Chang Gung University of Science and Technology, Taiwan (China)
  • 10. Department of Emergency Medicine, Cathay General Hospital, Taipei 10630, Taiwan (China)
  • 11. Institute of Traditional Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan (China)
  • 12. School of Medicine, Fu-Jen Catholic University, Taipei, Taiwan (China)

Description

Graphical abstract: - Highlights: • t-BHP's involvement in the ER stress pathway and liver cells injury. • ETFA as an important molecular target of t-BHP involving hepatotoxicity. • ETFA of t-BHP's action results in endoplasmic reticulum stress pathway. - Abstract: Tert-butyl hydroperoxide (t-BHP), an organic lipid hydroperoxide analog, has been demonstrated to exert pro-oxidant effects to evaluate mechanisms involving oxidative stress in hepatocyte cells and rat liver. Herein, we present an investigation of the event of molecular mechanism of t-BHP related acute liver injury. A proteomic approach was used to identify proteins which are differentially expressed in liver cells following t-BHP treatment and the mechanism of its action in apoptotic and endoplasmic reticulum stress pathways. Our results demonstrate that the t-BHP treatment of liver cells increased cell cytoxicity and apoptosis. t-BHP dose-dependent induction of cell apoptosis and stained liver sections relieved the acute rat liver injury were accompanied by sustained phosphorylation of JNK1/2 and p65. In addition, there were 13 differentially displayed proteins between the t-BHP-induced and untreated were assayed and validated in vivo. Furthermore, we demonstrated that t-BHP induced human Chang liver cell viability and apoptosis properties by up-regulating the levels of ETFA (electron transfer flavoprotein subunit alpha). This study demonstrated that there was an increase in the cellular levels of ETFA in the t-BHP induction in viability and apoptosis via the activation of JNK1/2 and NFκB signaling modules. NAC administration and shRNA ETFA conferred resistance to t-BHP-increased ETFA and CHOP expression via IRE1-alpha/TRAF2 complex formation, activation of JNK1/2 and p50. We concluded that the mechanism of t-BHP-induced an apoptosis cascade and endoplasmic reticulum stress in hepatocyte cells by up-regulation of ETFA, providing a new mechanism for liver injury

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tox.2013.12.007

Additional details

Identifiers

DOI
10.1016/j.tox.2013.12.007;
PII
S0300-483X(13)00339-9;

Publishing Information

Journal Title
Toxicology
Journal Volume
316
Journal Page Range
p. 61-70
ISSN
0300-483X
CODEN
TXCYAC

INIS

Country of Publication
Ireland
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47007806
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
APOPTOSIS; ENDOPLASMIC RETICULUM; IN VIVO; INJURIES; LIVER; LIVER CELLS; PHOSPHORYLATION; PROTEINS; RATS; STRESSES; VIABILITY
Descriptors DEC
ANIMAL CELLS; ANIMALS; BODY; CELL CONSTITUENTS; CHEMICAL REACTIONS; DIGESTIVE SYSTEM; DISEASES; GLANDS; MAMMALS; ORGANIC COMPOUNDS; ORGANS; RODENTS; SOMATIC CELLS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.