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肝内纤维蛋白(原)沉积驱动小鼠和人类肝部分切除术后的肝脏再生。

Intrahepatic fibrin(ogen) deposition drives liver regeneration after partial hepatectomy in mice and humans.

机构信息

Surgical Research Laboratory, Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI.

出版信息

Blood. 2019 Mar 14;133(11):1245-1256. doi: 10.1182/blood-2018-08-869057. Epub 2019 Jan 17.

Abstract

Platelets play a pivotal role in stimulating liver regeneration after partial hepatectomy in rodents and humans. Liver regeneration in rodents is delayed when platelets are inhibited. However, the exact mechanisms whereby platelets accumulate and promote liver regeneration remain uncertain. Thrombin-dependent intrahepatic fibrin(ogen) deposition was recently reported after partial hepatectomy (PHx) in mice, but the role of fibrin(ogen) deposits in liver regeneration has not been investigated. We tested the hypothesis that fibrin(ogen) contributes to liver regeneration by promoting intrahepatic platelet accumulation and identified the trigger of rapid intrahepatic coagulation after PHx. PHx in wild-type mice triggered rapid intrahepatic coagulation, evidenced by intrahepatic fibrin(ogen) deposition. Intrahepatic fibrin(ogen) deposition was abolished in mice with liver-specific tissue factor deficiency, pinpointing the trigger of coagulation after PHx. Direct thrombin activation of platelets through protease-activated receptor-4 did not contribute to hepatocyte proliferation after PHx, indicating that thrombin contributes to liver regeneration primarily by driving intrahepatic fibrin(ogen) deposition. Fibrinogen depletion with ancrod reduced both intrahepatic platelet accumulation and hepatocyte proliferation after PHx, indicating that fibrin(ogen) contributes to liver regeneration after PHx by promoting intrahepatic platelet accumulation. Consistent with the protective function of fibrin(ogen) in mice, low postoperative plasma fibrinogen levels were associated with liver dysfunction and mortality in patients undergoing liver resection. Moreover, increased intrahepatic fibrin(ogen) deposition was evident in livers of patients after liver resection but was remarkably absent in patients displaying hepatic dysfunction postresection. The results suggest a novel mechanism whereby coagulation-dependent intrahepatic fibrin(ogen) deposition drives platelet accumulation and liver regeneration after PHx.

摘要

血小板在啮齿动物和人类的肝部分切除术后刺激肝脏再生中起着关键作用。当血小板受到抑制时,啮齿动物的肝脏再生会延迟。然而,血小板聚集和促进肝脏再生的确切机制仍不清楚。最近有研究报道,在小鼠肝部分切除术后(PHx),肝内纤维蛋白原沉积依赖于凝血酶,但其在肝脏再生中的作用尚未得到研究。我们假设纤维蛋白原通过促进肝内血小板聚集促进肝脏再生,并确定 PHx 后肝内快速凝血的触发因素。在野生型小鼠中,PHx 触发了快速的肝内凝血,这可通过肝内纤维蛋白原沉积来证明。在组织因子特异性缺乏的小鼠中,肝内纤维蛋白原沉积被消除,这明确了 PHx 后凝血的触发因素。通过蛋白酶激活受体-4直接激活血小板的凝血酶并未促进 PHx 后肝细胞增殖,这表明凝血酶主要通过驱动肝内纤维蛋白原沉积来促进肝脏再生。用Ancrod 进行纤维蛋白原耗竭可减少 PHx 后肝内血小板聚集和肝细胞增殖,这表明纤维蛋白原通过促进肝内血小板聚集来促进 PHx 后的肝脏再生。与纤维蛋白原在小鼠中的保护作用一致,低术后血浆纤维蛋白原水平与接受肝切除术的患者的肝功能障碍和死亡率相关。此外,在肝切除术后患者的肝脏中可以明显看到纤维蛋白原沉积增加,但在术后显示肝功能障碍的患者中则明显不存在。这些结果表明了一种新的机制,即凝血依赖性肝内纤维蛋白原沉积驱动 PHx 后的血小板聚集和肝脏再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/561d/6418476/21a170c193d0/blood869057absf1.jpg

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