Bae Woo Kyun, Kang Keunsoo, Yu Ji Hoon, Yoo Kyung Hyun, Factor Valentina M, Kaji Kosuke, Matter Matthias, Thorgeirsson Snorri, Hennighausen Lothar
*Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, and Laboratory of Experimental Carcinogenesis, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA; Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea; Department of Microbiology, Dankook University, Cheonan, Korea; and New Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, Korea
*Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, and Laboratory of Experimental Carcinogenesis, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA; Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea; Department of Microbiology, Dankook University, Cheonan, Korea; and New Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, Korea.
FASEB J. 2015 May;29(5):1653-62. doi: 10.1096/fj.14-261537. Epub 2014 Dec 4.
To investigate the role of enhancer of zeste homolog (EZH) 1 and EZH2 in liver homeostasis, mice were generated that carried Ezh1(-/-) and EZH2(fl/fl) alleles and an Alb-Cre transgene. Only the combined loss of EZH1 and EZH2 in mouse hepatocytes caused a depletion of global trimethylation on Lys 27 of histone H3 (H3K27me3) marks and the specific loss of over ∼1900 genes at 3 mo of age. Ezh1(-/-),Ezh2(fl/fl)Alb-Cre mice exhibited progressive liver abnormalities manifested by the development of regenerative nodules and concomitant periportal fibrosis, inflammatory infiltration, and activation of A6-positive hepatic progenitor cells at 8 mo of age. In response to chronic treatment with carbon tetrachloride, all experimental mice, but none of the controls (n = 27 each), showed increased hepatic degeneration associated with liver dysfunction and reduced ability to proliferate. After two-thirds partial hepatectomy, mutant mice (n = 5) displayed increased liver injury and a blunted regenerative response. Genome-wide analyses at 3 mo of age identified 51 genes that had lost H3K27me3 marks, and their expression was significantly increased. These genes were involved in regulation of cell survival, fibrosis, and proliferation. H3K27me3 levels and liver physiology were unaffected in mice lacking either EZH1 globally or EZH2 specifically in hepatocytes. This work demonstrates a critical redundancy of EZH1 and EZH2 in maintaining hepatic homeostasis and regeneration.
为了研究zeste同源物增强子(EZH)1和EZH2在肝脏稳态中的作用,构建了携带Ezh1(-/-)和EZH2(fl/fl)等位基因以及Alb-Cre转基因的小鼠。仅小鼠肝细胞中EZH1和EZH2的联合缺失导致组蛋白H3赖氨酸27(H3K27me3)标记的整体三甲基化缺失,以及在3月龄时约1900个基因的特异性缺失。Ezh1(-/-)、Ezh2(fl/fl)Alb-Cre小鼠在8月龄时表现出进行性肝脏异常,表现为再生结节的形成以及伴随的门周纤维化、炎症浸润和A6阳性肝祖细胞的激活。在用四氯化碳进行慢性治疗后,所有实验小鼠(每组n = 27)均出现与肝功能障碍相关的肝变性增加和增殖能力降低,而对照组均未出现这种情况。在三分之二部分肝切除术后,突变小鼠(n = 5)表现出肝损伤增加和再生反应减弱。在3月龄时进行的全基因组分析确定了51个失去H3K27me3标记的基因,它们的表达显著增加。这些基因参与细胞存活、纤维化和增殖的调控。在肝细胞中特异性缺乏EZH1或EZH2的小鼠中,H3K27me3水平和肝脏生理功能未受影响。这项研究表明EZH1和EZH2在维持肝脏稳态和再生中具有关键的冗余作用。