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血小板刺激大鼠部分肝移植模型中的肝再生。

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

机构信息

Department of Gastrointestinal and Hepatobiliary-Pancreatic SurgeryGraduate School of Medicine University of Tsukuba Tsukuba Japan.

出版信息

Liver Transpl. 2021 May;27(5):719-734. doi: 10.1002/lt.25962.

Abstract

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.

摘要

活体肝移植(LDLT)有时会导致移植物再生受损和严重的缺血/再灌注损伤(IRI),从而导致小肝综合征(SFSS)。先前有研究报道血小板可刺激肝切除术模型中的肝再生,但在部分肝移植(LT)中缺乏证据。在这项研究中,使用大鼠部分 LT 模型,研究了血小板生成素(TPO)诱导的围手术期血小板增多对移植物再生、IRI 和存活率的影响。在实验 1 中,进行了 30%的部分 LT。在血小板增多的情况下,SFSS 减轻,表现为血清转氨酶、胆红素和腹水水平降低。血清肝细胞再生相关细胞因子,包括胰岛素样生长因子-1、肝细胞生长因子、白细胞介素 6(IL6)和肿瘤坏死因子 α(TNF-α),升高。此外,在血小板增多的情况下,增殖信号通路、Ki-67 标记指数、增殖细胞核抗原(PCNA)标记指数、有丝分裂指数和肝/体重比增加。血小板诱导的再生与 TPO 无关,因为在用 TPO 治疗的大鼠中通过抗血小板血清降低血小板计数后,Ki-67 标记和 PCNA 标记指数的增加被消除。对于 IRI,血小板增多并没有加重移植物中的氧化应激或下游信号通路、坏死或凋亡。在耗尽库普弗细胞(KC)后,血小板诱导的血清转氨酶降低、血清 IL6 和 TNF-α水平升高以及与增殖相关的信号通路被消除。此外,移植物中血小板的积聚大大减少。在实验 2 中,进行了 20%的部分 LT,血小板增多改善了术后存活率。总之,我们的结果表明,血小板增多刺激移植物再生并延长了部分 LT 后的生存时间,而不会加重 IRI,KC 对血小板衍生的再生至关重要。增加围手术期血小板计数的血小板治疗可能会改善 LDLT 的结果。

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