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
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