Ischemia reperfusion-facilitated sinusoidal endothelial cell injury in liver transplantation and the resulting impact of extravasated platelet aggregation.

IF 0.6 4区 医学 Q4 SURGERY
T Miyashita, S Nakanuma, A K Ahmed, I Makino, H Hayashi, K Oyama, H Nakagawara, H Tajima, H Takamura, I Ninomiya, S Fushida, J W Harmon, T Ohta
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引用次数: 43

Abstract

Background: The exact sequence of events leading to ultimate hepatocellular damage following ischemia/reperfusion (I/R) is incompletely understood. In this article, we review a mechanism of organ dysfunction after hepatic I/R or immunosuppressive treatment, in addition to the potential of liver sinusoidal endothelial cell (LSEC) protection and antiplatelet treatment for the suppression of hepatocellular damage.

Methods: A review of the literature, utilizing PubMed-NCBI, was used to provide information on the components necessary for the development of hepatocellular damage following I/R.

Results: It is well-established that LSECs damage following hepatic I/R or immunosuppressive treatment followed by extravasated platelet aggregation (EPA) is the root cause of organ dysfunction in liver transplantation. We have classified three phases, from LSECs damage to organ dysfunction, utilizing the predicted pathogenic mechanism of sinusoidal obstruction syndrome. The first phase is detachment of LSECs and sinusoidal wall destruction after LSECs injury by hepatic I/R or immunosuppressive treatment. The second phase is EPA, accomplished by sinusoidal wall destruction. The various growth factors, including thromboxane A2, serotonin, transforming growth factor-beta and plasminogen activator inhibitor-1, released by EPA in the Disse's space of zone three, induce portal hypertension and the progression of hepatic fibrosis. The third phase is organ dysfunction following portal hypertension, hepatic fibrosis, and suppressed liver regeneration through various growth factors secreted by EPA.

Conclusion: We suggest that EPA in the space of Disse, initiated by LSECs damage due to hepatic I/R or immunosuppressive treatment, and activated platelets may primarily contribute to liver damage in liver transplantation. Endothelial protective therapy or antiplatelet treatment may be useful in the treatment of hepatic I/R following EPA.

肝移植缺血再灌注诱导的血管内皮细胞损伤及其对血小板外渗聚集的影响。
背景:导致缺血/再灌注(I/R)后最终肝细胞损伤的事件的确切顺序尚不完全清楚。在本文中,我们综述了肝脏I/R或免疫抑制治疗后器官功能障碍的机制,以及肝窦内皮细胞(LSEC)保护和抗血小板治疗抑制肝细胞损伤的潜力。方法:利用PubMed-NCBI对文献进行回顾,以提供I/R后肝细胞损伤发展所需成分的信息。结果:肝脏I/R或免疫抑制治疗后血小板外渗性聚集(EPA)导致的LSECs损伤是肝移植器官功能障碍的根本原因。我们将LSECs损伤到器官功能障碍分为三个阶段,利用预测的窦状窦梗阻综合征的发病机制。第一阶段是肝I/R或免疫抑制治疗损伤LSECs后的LSECs脱离和窦壁破坏。第二阶段是EPA,由正弦壁破坏完成。各种生长因子,包括血栓素A2、血清素、转化生长因子- β和纤溶酶原激活物抑制剂-1,由EPA在第三区Disse空间释放,诱导门脉高压和肝纤维化的进展。第三阶段是门静脉高压症、肝纤维化和通过EPA分泌的各种生长因子抑制肝脏再生引起的器官功能障碍。结论:我们认为,由肝I/R或免疫抑制治疗导致的LSECs损伤引发的疾病空间EPA和活化的血小板可能是肝移植中肝损伤的主要原因。内皮保护治疗或抗血小板治疗可用于EPA后肝I/R的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
36
审稿时长
6-12 weeks
期刊介绍: The journal European Surgery – Acta Chirurgica Austriaca focuses on general surgery, endocrine surgery, thoracic surgery, heart and vascular surgery. Special features include new surgical and endoscopic techniques such as minimally invasive surgery, robot surgery, and advances in surgery-related biotechnology and surgical oncology. The journal especially addresses benign and malignant esophageal diseases, i.e. achalasia, gastroesophageal reflux disease, Barrett’s esophagus, and esophageal adenocarcinoma. In keeping with modern healthcare requirements, the journal’s scope includes inter- and multidisciplinary disease management (diagnosis, therapy and surveillance).
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