Diehl A M, Rai R M
Gastrointestinal Division, Johns Hopkins University School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.
FASEB J. 1996 Feb;10(2):215-27. doi: 10.1096/fasebj.10.2.8641555.
The liver has a tremendous capacity to regenerate. For example, after extensive hepatic resection, remaining hepatocytes proliferate to restore the mass of the organ within days to weeks. This proliferative response is fascinating because hepatocytes rarely replicate in the healthy adult liver. Instead, these cells perform highly specialized functions and exemplify mature, terminally differentiated cells. Therefore it is somewhat surprising that the liver can repopulate while performing its many obligate, organ-specific functions. Study of the regenerating liver remnant after partial hepatectomy has helped to delineate mechanisms that regulate proliferation and liver-specific functions in individual hepatocytes, as well as those that coordinate the behaviors of different liver cell populations to balance organ growth and tissue-specific gene expression. Hence, this review will focus on inter- and intracellular signals that regulate the hepatocyte phenotype after PH.
肝脏具有强大的再生能力。例如,在进行广泛的肝切除术后,剩余的肝细胞会增殖,在数天至数周内恢复器官的质量。这种增殖反应很有趣,因为肝细胞在健康的成年肝脏中很少复制。相反,这些细胞执行高度专业化的功能,是成熟的终末分化细胞的典范。因此,肝脏在执行其许多专一的、器官特异性功能的同时能够重新填充,这有点令人惊讶。对部分肝切除术后再生肝残余的研究有助于阐明调节单个肝细胞增殖和肝脏特异性功能的机制,以及协调不同肝细胞群体行为以平衡器官生长和组织特异性基因表达的机制。因此,本综述将聚焦于调节肝部分切除术后肝细胞表型的细胞间和细胞内信号。