Regulation of hepatocyte identity and quiescence

被引:49
作者
Berasain, Carmen [1 ]
Avila, Matias A. [1 ]
机构
[1] Univ Navarra, Inst Invest Sanitaria Navarra IdiSNA, CIBEREHD, Div Hepatol,CIMA, Pamplona 31008, Spain
关键词
Hepatocyte differentiation; Hepatocyte proliferation; Nuclear factors; Splicing regulator; Liver function; Hepatocellular carcinoma; Cirrhosis; NUCLEAR FACTOR 4-ALPHA; HUMAN HEPATOCELLULAR-CARCINOMA; CCAAT/ENHANCER-BINDING-PROTEIN; TRANSCRIPTION FACTOR NETWORK; LIVER DEVELOPMENT REQUIRES; TUMOR-SUPPRESSOR P53; GENE-EXPRESSION; S-ADENOSYLMETHIONINE; RAT HEPATOCYTES; CELL-PROLIFERATION;
D O I
10.1007/s00018-015-1970-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The liver is a highly differentiated organ with a central role in metabolism, detoxification and systemic homeostasis. To perform its multiple tasks, liver parenchymal cells, the hepatocytes, express a large complement of enabling genes defining their complex phenotype. This phenotype is progressively acquired during fetal development and needs to be maintained in adulthood to guarantee the individual's survival. Upon injury or loss of functional mass, the liver displays an extraordinary regenerative response, mainly based on the proliferation of hepatocytes which otherwise are long-lived quiescent cells. Increasing observations suggest that loss of hepatocellular differentiation and quiescence underlie liver malfunction in chronic liver disease and pave the way for hepatocellular carcinoma development. Here, we briefly review the essential mechanisms leading to the acquisition of liver maturity. We also identify the key molecular factors involved in the preservation of hepatocellular homeostasis and finally discuss potential strategies to preserve liver identity and function.
引用
收藏
页码:3831 / 3851
页数:21
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