肝细胞
细胞周期蛋白D1
基因敲除
调节器
再喂养综合征
细胞生长
肝再生
小发夹RNA
2-乙酰氨基芴
内科学
内分泌学
生物
医学
化学
细胞生物学
细胞周期
细胞凋亡
生物化学
营养不良
酶
癌症
再生(生物学)
体外
基因
微粒体
作者
Xuan Li,Shicheng Fan,Chenghui Cai,Yue Gao,Xinhui Wang,Yifei Zhang,Hangfei Liang,Huilin Li,Jie Yang,Min Huang,Huichang Bi
标识
DOI:10.1016/j.apsb.2022.12.011
摘要
Liver is the central hub regulating energy metabolism during feeding-fasting transition. Evidence suggests that fasting and refeeding induce dynamic changes in liver size, but the underlying mechanisms remain unclear. Yes-associated protein (YAP) is a key regulator of organ size. This study aims to explore the role of YAP in fasting- and refeeding-induced changes in liver size. Here, fasting significantly reduced liver size, which was recovered to the normal level after refeeding. Moreover, hepatocyte size was decreased and hepatocyte proliferation was inhibited after fasting. Conversely, refeeding promoted hepatocyte enlargement and proliferation compared to fasted state. Mechanistically, fasting or refeeding regulated the expression of YAP and its downstream targets, as well as the proliferation-related protein cyclin D1 (CCND1). Furthermore, fasting significantly reduced the liver size in AAV-control mice, which was mitigated in AAV Yap (5SA) mice. Yap overexpression also prevented the effect of fasting on hepatocyte size and proliferation. Besides, the recovery of liver size after refeeding was delayed in AAV Yap shRNA mice. Yap knockdown attenuated refeeding-induced hepatocyte enlargement and proliferation. In summary, this study demonstrated that YAP plays an important role in dynamic changes of liver size during fasting-refeeding transition, which provides new evidence for YAP in regulating liver size under energy stress.
科研通智能强力驱动
Strongly Powered by AbleSci AI