Literature DB >> 27113842

Cell-specific overactivation of nuclear erythroid 2 p45-related factor 2-mediated gene expression in myeloid cells decreases hepatic ischemia/reperfusion injury.

Lung-Yi Lee1, Calvin Harberg1, Kristina A Matkowskyj2,3, Shelly Cook2, Drew Roenneburg1, Sabine Werner4, Delinda A Johnson5,6, Jeffrey A Johnson5,6,7,8, David P Foley1,9.   

Abstract

Hepatic ischemia/reperfusion injury (IRI) is an unavoidable consequence of liver transplantation that can lead to postoperative hepatic dysfunction. Myeloid cells that include Kupffer cells, monocytes, and neutrophils contribute to the inflammatory response and cellular injury observed during hepatic IRI. We hypothesize that overactivation of the nuclear erythroid 2 p45-related factor 2 (Nrf2)-antioxidant response element (ARE) pathway in myeloid cells leads to decreased cellular damage after hepatic IRI. We constructed transgenic mice with constitutively active nuclear erythroid 2 p45-related factor 2 (caNrf2) that over activates the Nrf2-ARE pathway in myeloid cells (lysozyme M cre recombinase [LysMcre]+/caNrf2+, n = 9), and their littermate controls lacking transgene expression (LysMcre+/caNrf2-, n = 11). The mice underwent either sham or partial hepatic ischemia surgery, with 60 minutes of ischemia followed by 6 hours of reperfusion. After IRI, LysMcre+/caNrf2+ mice demonstrated significantly decreased serum alanine aminotransferase and decreased areas of necrosis. Immunohistochemistry and immunoblot of caspase 3 showed a significantly decreased cleaved to full-length caspase 3 ratio in LysMcre+/caNrf2+ animals. Lymphocyte antigen 6 complex locus G and CD68 staining demonstrated reduced inflammatory cell infiltration. LysMcre+/caNrf2+ animals also had significantly decreased gene expression of proinflammatory cytokines, including interleukin (IL) 1β, IL6, tumor necrosis factor α, chemokine (C-C motif) ligand 2, and chemokine (C-X-C motif) ligand 10, and significantly decreased levels of 8-isoprostanes. In our model, Nrf2 overactivation in myeloid cells leads to decreased hepatocellular damage, necrosis, apoptosis, inflammation, and oxidative stress. Pharmacologic targeting of the Nrf2-ARE pathway in myeloid cells may be a novel strategy to mitigate hepatic IRI. Liver Transplantation 22 1115-1128 2016 AASLD.
© 2016 American Association for the Study of Liver Diseases.

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Year:  2016        PMID: 27113842      PMCID: PMC5981012          DOI: 10.1002/lt.24473

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  37 in total

Review 1.  Preservation and reperfusion injuries in liver allografts. An overview and synthesis of current studies.

Authors:  P A Clavien; P R Harvey; S M Strasberg
Journal:  Transplantation       Date:  1992-05       Impact factor: 4.939

2.  Activated Nrf2 impairs liver regeneration in mice by activation of genes involved in cell-cycle control and apoptosis.

Authors:  Ulrike A Köhler; Svitlana Kurinna; Dominik Schwitter; Andrea Marti; Matthias Schäfer; Claus Hellerbrand; Tobias Speicher; Sabine Werner
Journal:  Hepatology       Date:  2014-06-18       Impact factor: 17.425

3.  An important function of Nrf2 in combating oxidative stress: detoxification of acetaminophen.

Authors:  K Chan; X D Han; Y W Kan
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-03       Impact factor: 11.205

4.  Neutrophil infiltration as an important factor in liver ischemia and reperfusion injury. Modulating effects of FK506 and cyclosporine.

Authors:  S Suzuki; L H Toledo-Pereyra; F J Rodriguez; D Cejalvo
Journal:  Transplantation       Date:  1993-06       Impact factor: 4.939

5.  Nrf2 activation protects the liver from ischemia/reperfusion injury in mice.

Authors:  Kazuhiro Kudoh; Hiroshi Uchinami; Masato Yoshioka; Ekihiro Seki; Yuzo Yamamoto
Journal:  Ann Surg       Date:  2014-07       Impact factor: 12.969

6.  KEAP1-NRF2 complex in ischemia-induced hepatocellular damage of mouse liver transplants.

Authors:  Bibo Ke; Xiu-Da Shen; Yu Zhang; Haofeng Ji; Feng Gao; Shi Yue; Naoko Kamo; Yuan Zhai; Masayuki Yamamoto; Ronald W Busuttil; Jerzy W Kupiec-Weglinski
Journal:  J Hepatol       Date:  2013-07-16       Impact factor: 25.083

7.  Identification of the NF-E2-related factor-2-dependent genes conferring protection against oxidative stress in primary cortical astrocytes using oligonucleotide microarray analysis.

Authors:  Jong-Min Lee; Marcus J Calkins; Kaimin Chan; Yuet Wai Kan; Jeffrey A Johnson
Journal:  J Biol Chem       Date:  2003-01-28       Impact factor: 5.157

8.  Risk factors for primary dysfunction after liver transplantation--a multivariate analysis.

Authors:  R J Ploeg; A M D'Alessandro; S J Knechtle; M D Stegall; J D Pirsch; R M Hoffmann; T Sasaki; H W Sollinger; F O Belzer; M Kalayoglu
Journal:  Transplantation       Date:  1993-04       Impact factor: 4.939

9.  Mitochondrial calcium uptake regulates cold preservation-induced Bax translocation and early reperfusion apoptosis.

Authors:  Christopher D Anderson; Andrey Belous; Janene Pierce; Ian B Nicoud; Clayton Knox; Aya Wakata; C Wright Pinson; Ravi S Chari
Journal:  Am J Transplant       Date:  2004-03       Impact factor: 8.086

10.  Cancer related mutations in NRF2 impair its recognition by Keap1-Cul3 E3 ligase and promote malignancy.

Authors:  Tatsuhiro Shibata; Tsutomu Ohta; Kit I Tong; Akiko Kokubu; Reiko Odogawa; Koji Tsuta; Hisao Asamura; Masayuki Yamamoto; Setsuo Hirohashi
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-29       Impact factor: 11.205

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  9 in total

Review 1.  p62/SQSTM1-Dr. Jekyll and Mr. Hyde that prevents oxidative stress but promotes liver cancer.

Authors:  Koji Taniguchi; Shinichiro Yamachika; Feng He; Michael Karin
Journal:  FEBS Lett       Date:  2016-08-06       Impact factor: 4.124

Review 2.  Targeting the Hepatic Microenvironment to Improve Ischemia/Reperfusion Injury: New Insights into the Immune and Metabolic Compartments.

Authors:  Fengqiang Gao; Xun Qiu; Kai Wang; Chuxiao Shao; Wenjian Jin; Zhen Zhang; Xiao Xu
Journal:  Aging Dis       Date:  2022-07-11       Impact factor: 9.968

3.  Intraperitoneal administration of apigenin in liver ischemia/reperfusion injury protective effects.

Authors:  Alexandra K Tsaroucha; Anastasia Tsiaousidou; Nikolaos Ouzounidis; Evanthia Tsalkidou; Maria Lambropoulou; Dimitrios Giakoustidis; Ekaterini Chatzaki; Constantinos Simopoulos
Journal:  Saudi J Gastroenterol       Date:  2016-11       Impact factor: 2.485

Review 4.  Pre-conditions for eliminating mitochondrial dysfunction and maintaining liver function after hepatic ischaemia reperfusion.

Authors:  Chenxia Hu; Lanjuan Li
Journal:  J Cell Mol Med       Date:  2017-03-16       Impact factor: 5.310

5.  N-Acetylcysteine Reduced Ischemia and Reperfusion Damage Associated with Steatohepatitis in Mice.

Authors:  Natalie Chaves Cayuela; Marcia Kiyomi Koike; Jacqueline de Fátima Jacysyn; Roberto Rasslan; Anderson Romério Azevedo Cerqueira; Soraia Katia Pereira Costa; José Antônio Picanço Diniz-Júnior; Edivaldo Massazo Utiyama; Edna Frasson de Souza Montero
Journal:  Int J Mol Sci       Date:  2020-06-09       Impact factor: 5.923

Review 6.  Regulation of Wound Healing by the NRF2 Transcription Factor-More Than Cytoprotection.

Authors:  Paul Hiebert; Sabine Werner
Journal:  Int J Mol Sci       Date:  2019-08-08       Impact factor: 5.923

7.  Immune-Responsive Gene 1/Itaconate Activates Nuclear Factor Erythroid 2-Related Factor 2 in Hepatocytes to Protect Against Liver Ischemia-Reperfusion Injury.

Authors:  Zhongjie Yi; Meihong Deng; Melanie J Scott; Guang Fu; Patricia A Loughran; Zhao Lei; Shilai Li; Ping Sun; Chenxuan Yang; Wenbo Li; Hongbo Xu; Feizhou Huang; Timothy R Billiar
Journal:  Hepatology       Date:  2020-10-12       Impact factor: 17.425

8.  Targeting p21-activated kinase 4 (PAK4) with pyrazolo[3,4-d]pyrimidine derivative SPA7012 attenuates hepatic ischaemia-reperfusion injury in mice.

Authors:  Yuancheng Mao; Eun Lee; Xiaohui Yang; Eun Ju Bae; Raok Jeon; Byung-Hyun Park
Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.756

9.  Nrf2 is highly expressed in neutrophils, but myeloid cell-derived Nrf2 is dispensable for wound healing in mice.

Authors:  Natasha Joshi; Sabine Werner
Journal:  PLoS One       Date:  2017-10-26       Impact factor: 3.240

  9 in total

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