Bird T G, Lorenzini S, Forbes S J
MRC/University of Edinburgh Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK.
Cell Tissue Res. 2008 Jan;331(1):283-300. doi: 10.1007/s00441-007-0542-z. Epub 2007 Nov 29.
The liver has enormous regenerative capacity. Following acute liver injury, hepatocyte division regenerates the parenchyma but, if this capacity is overwhelmed during massive or chronic liver injury, the intrinsic hepatic progenitor cells (HPCs) termed oval cells are activated. These HPCs are bipotential and can regenerate both biliary epithelia and hepatocytes. Multiple signalling pathways contribute to the complex mechanism controlling the behaviour of the HPCs. These signals are delivered primarily by the surrounding microenvironment. During liver disease, stem cells extrinsic to the liver are activated and bone-marrow-derived cells play a role in the generation of fibrosis during liver injury and its resolution. Here, we review our current understanding of the role of stem cells during liver disease and their mechanisms of activation.
肝脏具有巨大的再生能力。急性肝损伤后,肝细胞分裂可使实质再生,但在大规模或慢性肝损伤期间,如果这种能力不堪重负,被称为卵圆细胞的肝内固有祖细胞(HPC)就会被激活。这些HPC具有双向分化潜能,能够再生胆管上皮细胞和肝细胞。多种信号通路参与了控制HPC行为的复杂机制。这些信号主要由周围的微环境传递。在肝脏疾病期间,肝脏外的干细胞被激活,骨髓来源的细胞在肝损伤及其修复过程中纤维化的形成中发挥作用。在此,我们综述了目前对干细胞在肝脏疾病中的作用及其激活机制的理解。