Sudo Kaori, Yamada Yasuhiro, Saito Kuniaki, Shimizu Syogo, Ohashi Hazuki, Kato Tomohiro, Moriwaki Hisataka, Ito Hiroyasu, Seishima Mitsuru
Department of Informative Clinical Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan.
Biochim Biophys Acta. 2008 Nov;1782(11):671-9. doi: 10.1016/j.bbadis.2008.09.010. Epub 2008 Oct 2.
In the present study, we used bone marrow transplanted mice and revealed the role of bone marrow derived cells in liver regeneration after partial hepatectomy (PH). Irradiated wild type (WT) mice received a bone marrow transplant from either WT, TNF (tumor necrosis factor)-alpha knockout (KO), or interleukin (IL)-6 KO donors. Both TNF-alpha KO- and IL-6 KO-transplanted mice compared with WT-transplanted mice showed decreased hepatocyte DNA synthesis after PH. TNF-alpha KO-transplanted mice showed no nuclear factor kappa B (NF-kappaB) and signal transducer and activator of transcription (STAT) 3 binding after PH, while IL-6 KO-transplanted mice showed NF-kappaB, but not STAT3, binding. Lack of AP-1 or C/EBP binding or expression of c-jun or c-myc mRNA after PH was unrelated to the timing and amount of DNA replication. In conclusion, The TNF-alpha and IL-6 signals from the blood are necessary for liver regeneration and NF-kappaB and STAT3 binding are activated via TNF-alpha and IL-6 signal pathways.
在本研究中,我们使用骨髓移植小鼠,揭示了骨髓来源细胞在部分肝切除(PH)后肝脏再生中的作用。经照射的野生型(WT)小鼠接受来自WT、肿瘤坏死因子(TNF)-α基因敲除(KO)或白细胞介素(IL)-6基因敲除供体的骨髓移植。与WT移植小鼠相比,TNF-α基因敲除和IL-6基因敲除移植小鼠在PH后肝细胞DNA合成均减少。TNF-α基因敲除移植小鼠在PH后未显示核因子κB(NF-κB)和信号转导及转录激活因子(STAT)3结合,而IL-6基因敲除移植小鼠显示NF-κB结合,但未显示STAT3结合。PH后缺乏AP-1或C/EBP结合或c-jun或c-myc mRNA表达与DNA复制的时间和量无关。总之,血液中的TNF-α和IL-6信号是肝脏再生所必需的,且NF-κB和STAT3结合通过TNF-α和IL-6信号通路被激活。