Blockade of the Notch1/Jagged1 pathway in Kupffer cells aggravates ischemia-reperfusion injury of orthotopic liver transplantation in mice

被引:7
|
作者
Bai, He [1 ]
Wen, Jian [1 ]
Gong, Jian-Ping [1 ]
Wu, Hao [1 ]
Yuan, Fang-Chao [1 ]
Cao, Ding [1 ]
Wu, Ya-Kun [2 ]
Lai, Xing [3 ]
Wang, Meng-Hao [1 ]
机构
[1] Chongqing Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 2, 76 Linjiang St, Chongqing 400010, Peoples R China
[2] Suining Cent Hosp, Dept Hepatobiliary Surg, Suining, Sichuan, Peoples R China
[3] Tongnan Dist Peoples Hosp, Dept Hepatobiliary & Breast Surg, 271 Datong St, Chongqing 402660, Peoples R China
基金
中国国家自然科学基金;
关键词
Orthotopic liver transplantation; Kupffer cells; Notch1; Jagged1; pathway; Ischemia-reperfusion injury; TOLERANCE; JAGGED1; PTEN; INFLAMMATION; ACTIVATION; REJECTION; PROTECTS; REVERSAL; INSIGHTS;
D O I
10.1080/08916934.2019.1637424
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Liver ischemia-reperfusion injury (IRI) represents a risk factor for early graft dysfunction and an obstacle to expanding donor pool in orthotopic liver transplantation (OLT). Kupffer cells (KCs) are the largest antigen-presenting cell (APC) group and the primary modulators of inflammation in liver tissues. The vital role of Notch1/Jagged1 pathway in mouse OLT model has been reported, however, its potential therapeutic mechanism is unknown. Here, we made use of short hairpin RNA-Jagged1 and AAV-Jagged1 to explore the effects of Notch1/Jagged1 pathway in OLT. In vitro, blockade of Notch1/Jagged1 pathway downregulated the expression of Hairy and enhancer of split-1 (Hes1) gene, which in turn increased the proinflammatory effects of KCs. Moreover, the anti-inflammatory effects of Notch1/Jagged1 pathway were induced by inhibiting Hes1/gene of phosphate and tension/protein kinase B/Toll-like receptor 4/nuclear factor kappa B (Hes1/PTEN/AKT/TLR4/NF-kappa B) axis in KCs. In vivo, we used a well-established mouse model of OLT to mimic clinical transplantation. Mice were stochastically divided into 6 groups: Sham group (n = 15); Normal saline (NS) group (n = 15); Adeno-associated virus-green fluorescent protein (AAV-GFP) group (n = 15); AAV-Jagged1 group (n = 15); Clodronate liposome (CL) group (n = 15); CL+AAV-Jagged1 group (n = 15) . After OLT the liver damage in AAV-Jagged1 group were significantly accentuated compared to the AAV-GFP group. While blockade of Jagged1 aftet clearence of KCs by CL would not lead to further liver injuries. Taken together, our study demonstrated that blockade of Notch1/Jagged1 pathway aggravates inflammation induced by lipopolysaccharide (LPS) via Hes1/PTEN/AKT/TLR4/NF-kappa B in KCs, and the blockade of Notch1/Jagged1 pathway in donor liver increased neutrophil/macrophage infiltration and hepatocellular apoptosis, which suggested the function of Notch1/Jagged1 pathway in mouse OLT and highlighted the protective function of Notch1/Jagged1 pathway in liver transplantation.
引用
收藏
页码:176 / 184
页数:9
相关论文
共 50 条
  • [1] Nobiletin ameliorates ischemia-reperfusion injury by suppressing the function of Kupffer cells after liver transplantation in rats
    Wu, Yakun
    Zhang, Wenfeng
    Li, Min
    Cao, Ding
    Yang, Xiaoli
    Gong, Jianping
    BIOMEDICINE & PHARMACOTHERAPY, 2017, 89 : 732 - 741
  • [2] Exosomes derived from TGF-81-pretreated mesenchymal stem cells alleviate biliary ischemia-reperfusion injury through Jagged1/Notch1/SOX9 pathway
    Yasen, Aimaiti
    Feng, Jun
    Xie, Xing -Ming
    Li, Kai
    Cai, Yu -Hong
    Liao, Zhi-Hong
    Liang, Run -Bin
    Dai, Tian -Xing
    Wang, Guo-Ying
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 119
  • [3] Preactivation of Notch1 in remote ischemic preconditioning reduces cerebral ischemia-reperfusion injury through crosstalk with the NF-κB pathway
    Liang, Weidong
    Lin, Chunshui
    Yuan, Liuqing
    Chen, Li
    Guo, Peipei
    Li, Ping
    Wang, Wei
    Zhang, Xin
    JOURNAL OF NEUROINFLAMMATION, 2019, 16 (01)
  • [4] IRE1α aggravates ischemia reperfusion injury of fatty liver by regulating phenotypic transformation of kupffer cells
    Yang, Faji
    Wang, Shuai
    Liu, Yang
    Zhou, Yuan
    Shang, Longcheng
    Feng, Min
    Yuan, Xianwen
    Zhu, Wei
    Shi, Xiaolei
    FREE RADICAL BIOLOGY AND MEDICINE, 2018, 124 : 395 - 407
  • [5] Activation of PPARγ by Curcumin protects mice from ischemia/reperfusion injury induced by orthotopic liver transplantation via modulating polarization of Kupffer cells
    Liu, Yan
    Zhang, Wenfeng
    Cheng, Yao
    Miao, Chunmu
    Gong, Jianping
    Wang, Menghao
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2018, 62 : 270 - 276
  • [6] MicroRNA-155 Deficiency in Kupffer Cells Ameliorates Liver Ischemia-Reperfusion Injury in Mice
    Li, Yakun
    Ma, Dongxia
    Wang, Zhimin
    Yang, Jun
    TRANSPLANTATION, 2017, 101 (07) : 1600 - 1608
  • [7] Dexmedetomidine alleviates myocardial ischemia-reperfusion injury by down-regulating miR-34b-3p to activate the Jagged1/Notch signaling pathway
    Guo, Peng
    Yi, Han
    Han, Mingming
    Liu, Xinxin
    Chen, Kemin
    Qing, Jie
    Yang, Fengrui
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 116
  • [8] TGR5 Attenuated Liver Ischemia-Reperfusion Injury by Activating the Keap1-Nrf2 Signaling Pathway in Mice
    Zhuang, Lin
    Ding, Wenbin
    Zhang, Qi
    Ding, Wei
    Xu, Xuezhong
    Yu, Xiaolong
    Xi, Dong
    INFLAMMATION, 2021, 44 (03) : 859 - 872
  • [9] Treprostinil, a Prostacyclin Analog, Ameliorates Ischemia-Reperfusion Injury in Rat Orthotopic Liver Transplantation
    Ghonem, N.
    Yoshida, J.
    Stolz, D. B.
    Humar, A.
    Starzl, T. E.
    Murase, N.
    Venkataramanan, R.
    AMERICAN JOURNAL OF TRANSPLANTATION, 2011, 11 (11) : 2508 - 2516
  • [10] HSP110 aggravates ischemia-reperfusion injury after liver transplantation by promoting NF- κ B pathway
    Hu, Qing-Zhi
    Cao, Zhen-Rui
    Zheng, Wei-Xiong
    Zhao, Min-Jie
    Gong, Jun-Hua
    Chen, Cong
    Wu, Zhong-Jun
    Tao, Rui
    HEPATOBILIARY & PANCREATIC DISEASES INTERNATIONAL, 2024, 23 (04) : 344 - 352