GBP1 promotes acute rejection after liver transplantation by inducing Kupffer cells pyroptosis

Liver transplantation is currently recognized as the most effective treatment for severe liver diseases. Although survival rates after liver transplantation have improved, rejection of the transplanted liver remains a significant cause of morbidity and transplant failure in patients. Our team previously discovered a close association between high GBP1 expression and acute rejection reactions following liver transplantation. Liver biopsies were conducted on patients who experienced acute rejection or successfully achieved immune tolerance post-transplantation. We confirmed that GBP1 was highly expressed in the acute rejection group after transplantation by Immunohistochemistry. This study aims to confirm that GBP1 promotes acute rejection reactions following liver transplantation through inducing pyroptosis in rat transplanted hepatic macrophages (KCs). We knocked down GBP1 in KCs and examined the extent of pyroptosis and the severity of acute rejection in the transplanted liver post-orthotopic liver transplantation in rats and KCs. These data provide new approaches for the study of liver transplant rejection reactions and identify new targets.

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Publication Details

Journal
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Published
2024-12-26
DOI
https://doi.org/10.1016/j.bbadis.2024.167644
Citations
5
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
1.17
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article

GBP1 promotes acute rejection after liver transplantation by inducing Kupffer cells pyroptosis

Kairui Lu, Yan Wang, Li Zhang, Jun Xu et al.
5 citations
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Inflammasome and immune disorders
1.17
article

GBP1 promotes acute rejection after liver transplantation by inducing Kupffer cells pyroptosis

Kairui Lu, Yan Wang, Li Zhang, Jun Xu, Qingyao Chang, Huaxing Ding, Wenhao Shao, Haojiang Duan
article en
5 citations

Abstract

Liver transplantation is currently recognized as the most effective treatment for severe liver diseases. Although survival rates after liver transplantation have improved, rejection of the transplanted liver remains a significant cause of morbidity and transplant failure in patients. Our team previously discovered a close association between high GBP1 expression and acute rejection reactions following liver transplantation. Liver biopsies were conducted on patients who experienced acute rejection or successfully achieved immune tolerance post-transplantation. We confirmed that GBP1 was highly expressed in the acute rejection group after transplantation by Immunohistochemistry. This study aims to confirm that GBP1 promotes acute rejection reactions following liver transplantation through inducing pyroptosis in rat transplanted hepatic macrophages (KCs). We knocked down GBP1 in KCs and examined the extent of pyroptosis and the severity of acute rejection in the transplanted liver post-orthotopic liver transplantation in rats and KCs. These data provide new approaches for the study of liver transplant rejection reactions and identify new targets.

Biochimica et Biophysica Acta (BBA) - Molecular Basis of DiseaseVol. 1871(3)
Shanxi Medical University (CN)
Zero hunger
Openalex Percentile: Top 21%
Inflammasome and immune disorders
1.17
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