Choijookhuu Narantsog, Yano Koichi, Lkham-Erdene Baljinnyam, Shirouzu Shinichiro, Kubota Toshiki, Ishizuka Takumi, Kai Kengo, Chosa Etsuo, Hishikawa Yoshitaka
Department of Anatomy, Histochemistry and Cell Biology.
Faculty of Medicine, University of Miyazaki, Miyazaki, Japan; and Department of Pathology and Forensic Medicine, School of Biomedicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia.
J Histochem Cytochem. 2024 Apr;72(4):245-264. doi: 10.1369/00221554241241569. Epub 2024 Mar 27.
Liver regeneration is a well-orchestrated compensatory process that is regulated by multiple factors. We recently reported the importance of the chromatin protein, a high-mobility group box 2 (HMGB2) in mouse liver regeneration. However, the molecular mechanism remains unclear. In this study, we aimed to study how HMGB2 regulates hepatocyte proliferation during liver regeneration. Seventy-percent partial hepatectomy (PHx) was performed in wild-type (WT) and HMGB2-knockout (KO) mice, and the liver tissues were used for microarray, immunohistochemistry, quantitative polymerase chain reaction (qPCR), and Western blotting analyses. In the WT mice, HMGB2-positive hepatocytes colocalized with cell proliferation markers. In the HMGB2-KO mice, hepatocyte proliferation was significantly decreased. Oil Red O staining revealed the transient accumulation of lipid droplets at 12-24 hr after PHx in the WT mouse livers. In contrast, decreased amount of lipid droplets were found in HMGB2-KO mouse livers, and it was preserved until 36 hr. The microarray, immunohistochemistry, and qPCR results demonstrated that the expression of lipid metabolism-related genes was significantly decreased in the HMGB2-KO mouse livers. The in vitro experiments demonstrated that a decrease in the amount of lipid droplets correlated with decreased cell proliferation activity in HMGB2-knockdown cells. HMGB2 promotes de novo lipogenesis to accelerate hepatocyte proliferation during liver regeneration.
肝脏再生是一个由多种因素调控的精心编排的代偿过程。我们最近报道了染色质蛋白高迁移率族盒蛋白2(HMGB2)在小鼠肝脏再生中的重要性。然而,其分子机制仍不清楚。在本研究中,我们旨在研究HMGB2在肝脏再生过程中如何调节肝细胞增殖。对野生型(WT)和HMGB2基因敲除(KO)小鼠进行70%的部分肝切除术(PHx),并将肝脏组织用于微阵列、免疫组织化学、定量聚合酶链反应(qPCR)和蛋白质印迹分析。在WT小鼠中,HMGB2阳性肝细胞与细胞增殖标志物共定位。在HMGB2-KO小鼠中,肝细胞增殖显著降低。油红O染色显示,在WT小鼠肝脏中,PHx后12-24小时脂滴短暂积累。相比之下,在HMGB2-KO小鼠肝脏中发现脂滴数量减少,并且这种情况一直持续到36小时。微阵列、免疫组织化学和qPCR结果表明,HMGB2-KO小鼠肝脏中脂质代谢相关基因的表达显著降低。体外实验表明,HMGB2基因敲低细胞中脂滴数量的减少与细胞增殖活性的降低相关。HMGB2在肝脏再生过程中促进从头脂肪生成以加速肝细胞增殖。