Platelets Stimulate Liver Regeneration in a Rat Model of Partial Liver Transplantation

Living donor liver transplantation (LDLT) is sometimes associated with impaired regeneration and severe ischemia/reperfusion injury (IRI) in the graft, resulting in small‐for‐size syndrome (SFSS). Platelets were previously reported to stimulate liver regeneration in models of hepatectomy, but the ev...

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Veröffentlicht in:Liver transplantation 2021-05, Vol.27 (5), p.719-734
Hauptverfasser: Liang, Chen, Takahashi, Kazuhiro, Furuya, Kinji, Oda, Tatsuya, Ohkohchi, Nobuhiro
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container_end_page 734
container_issue 5
container_start_page 719
container_title Liver transplantation
container_volume 27
creator Liang, Chen
Takahashi, Kazuhiro
Furuya, Kinji
Oda, Tatsuya
Ohkohchi, Nobuhiro
description Living donor liver transplantation (LDLT) is sometimes associated with impaired regeneration and severe ischemia/reperfusion injury (IRI) in the graft, resulting in small‐for‐size syndrome (SFSS). Platelets were previously reported to stimulate liver regeneration in models of hepatectomy, but the evidence in partial liver transplantation (LT) is lacking. In this study, a rat model of partial LT was used, and the impact of thrombopoietin (TPO)‐induced perioperative thrombocytosis on graft regeneration, IRI, and survival was investigated. In experiment 1, a 30% partial LT was performed. Under thrombocytosis, SFSS was attenuated, as shown by decreased levels of serum aminotransferases, bilirubin, and ascites. Serum hepatocyte regeneration–related cytokines, including insulin‐like growth factor‐1, hepatocyte growth factor, interleukin 6 (IL6), and tumor necrosis factor α (TNF‐α), were elevated. In addition, the proliferative signaling pathways, Ki‐67‐labeling index, proliferating cell nuclear antigen (PCNA)–labeling index, mitotic index, and liver/body weight ratio were increased under thrombocytosis. The platelet‐induced regeneration was independent of TPO because increases in the Ki‐67‐labeling and PCNA‐labeling indexes were eliminated after reducing platelet counts by antiplatelet serum in rats administered with TPO. For IRI, thrombocytosis did not aggravate oxidative stress or downstream signaling pathways, necrosis, or apoptosis in the graft. After Kupffer cell (KC) depletion, the platelet‐induced attenuation of serum aminotransferases, increased serum levels of IL6 and TNF‐α, and proliferation‐related signaling pathways were eliminated. Moreover, platelet accumulation in the graft decreased substantially. In experiment 2, a 20% partial LT was performed, and thrombocytosis improved postoperative survival. In conclusion, our results suggested that thrombocytosis stimulated graft regeneration and prolonged survival without aggregating IRI after partial LT, and KCs vitally contributed to platelet‐derived regeneration. Platelet therapies to increase perioperative platelet counts may improve the outcomes after LDLT. https://www.wileyhealthlearning.com/Activity2/7346145/Activity.aspx
doi_str_mv 10.1002/lt.25962
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Platelets were previously reported to stimulate liver regeneration in models of hepatectomy, but the evidence in partial liver transplantation (LT) is lacking. In this study, a rat model of partial LT was used, and the impact of thrombopoietin (TPO)‐induced perioperative thrombocytosis on graft regeneration, IRI, and survival was investigated. In experiment 1, a 30% partial LT was performed. Under thrombocytosis, SFSS was attenuated, as shown by decreased levels of serum aminotransferases, bilirubin, and ascites. Serum hepatocyte regeneration–related cytokines, including insulin‐like growth factor‐1, hepatocyte growth factor, interleukin 6 (IL6), and tumor necrosis factor α (TNF‐α), were elevated. In addition, the proliferative signaling pathways, Ki‐67‐labeling index, proliferating cell nuclear antigen (PCNA)–labeling index, mitotic index, and liver/body weight ratio were increased under thrombocytosis. The platelet‐induced regeneration was independent of TPO because increases in the Ki‐67‐labeling and PCNA‐labeling indexes were eliminated after reducing platelet counts by antiplatelet serum in rats administered with TPO. For IRI, thrombocytosis did not aggravate oxidative stress or downstream signaling pathways, necrosis, or apoptosis in the graft. After Kupffer cell (KC) depletion, the platelet‐induced attenuation of serum aminotransferases, increased serum levels of IL6 and TNF‐α, and proliferation‐related signaling pathways were eliminated. Moreover, platelet accumulation in the graft decreased substantially. In experiment 2, a 20% partial LT was performed, and thrombocytosis improved postoperative survival. In conclusion, our results suggested that thrombocytosis stimulated graft regeneration and prolonged survival without aggregating IRI after partial LT, and KCs vitally contributed to platelet‐derived regeneration. 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The platelet‐induced regeneration was independent of TPO because increases in the Ki‐67‐labeling and PCNA‐labeling indexes were eliminated after reducing platelet counts by antiplatelet serum in rats administered with TPO. For IRI, thrombocytosis did not aggravate oxidative stress or downstream signaling pathways, necrosis, or apoptosis in the graft. After Kupffer cell (KC) depletion, the platelet‐induced attenuation of serum aminotransferases, increased serum levels of IL6 and TNF‐α, and proliferation‐related signaling pathways were eliminated. Moreover, platelet accumulation in the graft decreased substantially. In experiment 2, a 20% partial LT was performed, and thrombocytosis improved postoperative survival. In conclusion, our results suggested that thrombocytosis stimulated graft regeneration and prolonged survival without aggregating IRI after partial LT, and KCs vitally contributed to platelet‐derived regeneration. 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Platelets were previously reported to stimulate liver regeneration in models of hepatectomy, but the evidence in partial liver transplantation (LT) is lacking. In this study, a rat model of partial LT was used, and the impact of thrombopoietin (TPO)‐induced perioperative thrombocytosis on graft regeneration, IRI, and survival was investigated. In experiment 1, a 30% partial LT was performed. Under thrombocytosis, SFSS was attenuated, as shown by decreased levels of serum aminotransferases, bilirubin, and ascites. Serum hepatocyte regeneration–related cytokines, including insulin‐like growth factor‐1, hepatocyte growth factor, interleukin 6 (IL6), and tumor necrosis factor α (TNF‐α), were elevated. In addition, the proliferative signaling pathways, Ki‐67‐labeling index, proliferating cell nuclear antigen (PCNA)–labeling index, mitotic index, and liver/body weight ratio were increased under thrombocytosis. The platelet‐induced regeneration was independent of TPO because increases in the Ki‐67‐labeling and PCNA‐labeling indexes were eliminated after reducing platelet counts by antiplatelet serum in rats administered with TPO. For IRI, thrombocytosis did not aggravate oxidative stress or downstream signaling pathways, necrosis, or apoptosis in the graft. After Kupffer cell (KC) depletion, the platelet‐induced attenuation of serum aminotransferases, increased serum levels of IL6 and TNF‐α, and proliferation‐related signaling pathways were eliminated. Moreover, platelet accumulation in the graft decreased substantially. In experiment 2, a 20% partial LT was performed, and thrombocytosis improved postoperative survival. In conclusion, our results suggested that thrombocytosis stimulated graft regeneration and prolonged survival without aggregating IRI after partial LT, and KCs vitally contributed to platelet‐derived regeneration. 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subjects Animals
Apoptosis
Ascites
Bilirubin
Blood Platelets
Body weight
Growth factors
Hepatectomy
Hepatocyte growth factor
Humans
Insulin
Interleukin 6
Ischemia
Labeling
Liver
Liver Regeneration
Liver transplantation
Liver Transplantation - adverse effects
Liver transplants
Living Donors
Oxidative stress
Platelets
Proliferating cell nuclear antigen
Rats
Reperfusion
Serum levels
Signal transduction
Thrombocytosis
Thrombopoietin
Tumor necrosis factor-TNF
Tumor necrosis factor-α
title Platelets Stimulate Liver Regeneration in a Rat Model of Partial Liver Transplantation
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