Role of plasminogen in macrophage accumulation during liver repair

被引:16
作者
Kawao, Naoyuki [1 ]
Nagai, Nobuo [1 ]
Okada, Kiyotaka [1 ]
Okumoto, Katsumi [2 ]
Ueshima, Shigeru [1 ,3 ]
Matsuo, Osamu [1 ]
机构
[1] Kinki Univ, Sch Med, Dept Physiol, Osakasayama 5898511, Japan
[2] Kinki Univ, Sch Med, Ctr Morphol Anal Cent Res Facil, Osakasayama 5898511, Japan
[3] Kinki Univ, Sch Agr, Dept Food Sci & Nutr, Nara 6318505, Japan
基金
日本学术振兴会;
关键词
Plasminogen; Macrophage accumulation; Traumatic liver injury; Hepatic ischemia-reperfusion injury; Liver repair; DEFICIENCY LEADS; MICE; INJURY; ACTIVATION; SYSTEM; REGENERATION; HEPATOCYTES; MECHANISMS; EXPRESSION; MONOCYTES;
D O I
10.1016/j.thromres.2009.12.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Although the involvement of plasminogen in liver repair has been reported, its roles are still poorly understood. Here, we investigated the role of plasminogen in accumulations of macrophages and neutrophils after liver injury in mice with gene deficient of plasminogen (Plg(-/-)) or its wild type (Plg(+/+)). Materials and Methods: Mice received traumatic liver injury caused by stabbing on the lobe or hepatic ischemia-reperfusion, and the damaged sites were histologically analyzed. Results: After the traumatic liver injury, both the stab wound and the damaged tissue were decreased until day 7 in the Plg(+/+) mice. In contrast, both the stab wound and the damaged tissue were still remained until day 7 in the Plg(-/-) mice. On day 4 after traumatic liver injury, macrophages were abundant at the surrounding area of the damaged site in the Plg(+/+) mice. However, the macrophage accumulation was impaired in the Plg(-/-) mice. After hepatic ischemia-reperfusion injury, macrophage accumulation and decrease in the damaged tissue were also observed in the Plg(+/+) mice until day 7. In contrast, these responses were also impaired in the Plg(-/-) mice. Furthermore, neutrophil accumulation at the surrounding area of the damaged site was also impaired in the Plg(-/-) mice on day 4 after both liver traumatic liver injury and hepatic ischemia-reperfusion injury. Conclusions: Our data indicate that plasminogen plays a crucial role in macrophage accumulation together with the neutrophil accumulation after liver injury in both models, which may be essential for triggering the subsequent healing responses including decrease in the damaged tissue. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:E214 / E221
页数:8
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