纤溶酶原缺陷小鼠部分肝切除术后肝脏再生受损

M. Tanaka , K. Okada , S. Ueshima , M. Imano , H. Ohyanagi , P. Carmeliet , O. Matsuo
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引用次数: 10

摘要

肝脏再生受到多种生长因子的调节。这些生长因子的释放和激活与细胞外基质(ECM)的降解密切相关,而细胞外基质的降解受纤溶酶原激活系统的调节。由于纤溶酶原被认为在肝脏再生的这些功能中是必不可少的,因此对纤溶酶原缺乏型(Plg−/-)小鼠和野生型(Plg+/+)小鼠进行了70%的部分肝切除术(PH)。在Plg+/+小鼠中,70%PH后肝脏重量的顺序恢复在1至14天内逐渐增加。然而,在Plg−/−小鼠中,它在1至7天内增加,此后不再增加。因此,与Plg+/+小鼠相比,Plg−/-小鼠在第10天和第14天的恢复明显受损。Plg+/+小鼠在5天内表现出DNA合成增加,然后下降;然而,在Plg−/−小鼠中,它在3天内增加,然后下降,在14天时显著下降。在Plg+/+小鼠中,凋亡细胞核标记指数在3天内略有增加,此后下降。在Plg−/−小鼠中,在3天内很少检测到,在7至14天内逐渐增加。第14天,Plg−/-小鼠的凋亡指数高于Plg+/+小鼠。在肝脏的组织学检查中,在PH后的Plg−/-小鼠中检测到伴有纤维蛋白沉积的细胞损失的局灶性区域,而在Plg+/+小鼠中很少检测到。在Plg−/−小鼠中,与Plg+/+小鼠相比,在PH后14天,肝脏中t-PA、u-PA和pro-MMP-9的表达增加。这些发现表明纤溶酶原在PH后的肝脏再生中起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impaired liver regeneration after partial hepatectomy in plasminogen deficient mice
Abstract Liver regeneration is regulated by variety of growth factors. Release and activation of these growth factors are deeply related to degradation of extracellular matrix (ECM), which is regulated by plasminogen-activating system. Since plasminogen is assum ed to be essential in these functions in liver regeneration, partial 70% hepatectomy (PH) was performed on plasminogen deficient (Plg−/−) mice and wild-type (Plg+/+) mice. The sequential recovery of the liver weight after 70% PH gradually increased over 1 to 14 days in Plg+/+ mice. However, in Plg−/− mice, it increased over 1 to 7 days and thereafter increased no more. Thus, the recovery in Plg−/− mice was significantly impaired at 10 and 14 days compared with Plg+/+ mice. Plg+/+ mice exhibited an increase in DNA synthesis over5 days, and then a decrease thereafter; however, in Plg−/− mice, it increased over 3 days, and decreased thereafter, with the significant decrease at 14 days. The apoptotic nuclei labelling index slightly increased over 3 days, and decreased thereafter in Plg+/+ mice. In Plg−/− mice, it was few detected over 3 days, and gradually increased over 7 to 14 days. The apoptotic index in Plg−/− mice was higher than Plg+/+ mice at 14 days. In the histological examination of liver, focal area of cellular loss with fibrin deposition were detected in Plg−/− mice after PH, which were rarely detected in Plg+/+ mice. In Plg−/− mice, expressions of t-PA, u-PA and pro-MMP-9 were increased in the liver at 14 days after PH compared with Plg+/+ mice. These findings suggest that plasminogen plays an important role in liver regeneration after PH.
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