Arioka Yuko, Ito Hiroyasu, Ando Tatsuya, Ogiso Hideyuki, Hirata Akihiro, Hara Akira, Seishima Mitsuru
Department of Informative Clinical Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan,
Dig Dis Sci. 2015 Jun;60(6):1699-706. doi: 10.1007/s10620-015-3536-9. Epub 2015 Jan 29.
The liver has a high capacity of its regeneration. Most hepatic cells are quiescent unless otherwise stimulated such as their injury or ablation. A previous study suggest that pre-activated hepatic cells have a positive effect on their regeneration. In this study, we examined whether the pre-activated hepatic cells for regeneration accelerate the subsequent liver regeneration.
We administered a single injection of carbon tetrachloride (CCl4) to mice 7 days before partial hepatectomy (PHx). Liver weight/body weight ratio and several parameters for cell proliferation such as mitotic index and the number of Ki67 positive cells in the liver were examined after PHx as indexes of liver regeneration.
Compared to control mice, those pre-stimulated with CCl4 showed earlier liver regeneration 48 h after PHx. Regardless of their accelerated regeneration, pre-stimulated mice showed less cell proliferation than did control mice during liver regeneration. Hepatic fibrosis was not observed in both control and CCl4-pretreated mice after PHx. Mice pre-treated with CCl4 showed the higher matrix metalloproteinase 9 (MMP9) expression than those pre-treated with olive oil. When matrix metalloproteinase 9 (MMP9) activity was inhibited, the pre-stimulated mice did not demonstrate accelerated liver regeneration and they returned to the original state for cell proliferations after PHx.
Pre-activated liver by CCl4 promoted its subsequent regeneration after PHx. This was not a cause of fibrosis and partly dependent on MMP9 pre-activity rather than cell proliferation in liver. Our findings would not only provide a novel strategy for liver regeneration without cell proliferation as much as possible and also propose a new method for liver transplantation.
肝脏具有强大的再生能力。大多数肝细胞处于静止状态,除非受到损伤或切除等刺激。先前的一项研究表明,预先激活的肝细胞对其再生具有积极作用。在本研究中,我们检测了用于再生的预先激活的肝细胞是否能加速随后的肝脏再生。
在部分肝切除(PHx)前7天给小鼠单次注射四氯化碳(CCl4)。以肝重/体重比以及细胞增殖的几个参数,如有丝分裂指数和肝脏中Ki67阳性细胞数量,作为肝脏再生的指标,在PHx后进行检测。
与对照小鼠相比,用CCl4预先刺激的小鼠在PHx后48小时肝脏再生更早。尽管再生加速,但在肝脏再生期间,预先刺激的小鼠细胞增殖比对照小鼠少。PHx后,对照小鼠和CCl4预处理小鼠均未观察到肝纤维化。用CCl4预处理的小鼠比用橄榄油预处理的小鼠基质金属蛋白酶9(MMP9)表达更高。当基质金属蛋白酶9(MMP9)活性受到抑制时,预先刺激的小鼠未表现出加速的肝脏再生,并且在PHx后细胞增殖恢复到原始状态。
CCl4预先激活的肝脏促进了PHx后的后续再生。这不是纤维化的原因,部分依赖于MMP9的预先活性而非肝脏中的细胞增殖。我们的发现不仅将提供一种尽可能不依赖细胞增殖的肝脏再生新策略,还将提出一种肝脏移植的新方法。