Sun Zhongtao, Chen Guobao
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Tissue Cell. 2024 Dec;91:102559. doi: 10.1016/j.tice.2024.102559. Epub 2024 Sep 12.
Liver fibrosis is a disease with a high prevalence worldwide. The development of hepatic fibrosis results from a combination of factors within the liver, such as extracellular matrix (ECM) deposition, hepatic stellate cells (HSCs) activation, collagen cross-linking, and inflammatory response. Heterogeneity in fibrotic liver is the result of a combination of heterogeneity in the intrahepatic microenvironment as well as heterogeneous expression of fibrosis-associated enzymes and cells, complicating the study of the mechanisms underlying the progression of liver fibrosis. The role of this heterogeneity on the crosstalk between cells and matrix and on the fibrotic process is worth exploring. In this paper, we will describe the phenomenon and mechanism of heterogeneity of liver matrix and intrahepatic cells in the process of hepatic fibrosis and discuss the crosstalk between heterogeneous factors on the development of fibrosis. The elucidation of heterogeneity is important for a deeper understanding of the pathological mechanisms of liver fibrosis as well as for clinical diagnosis and targeted therapies.
肝纤维化是一种在全球范围内具有高患病率的疾病。肝纤维化的发展是由肝脏内多种因素共同作用导致的,如细胞外基质(ECM)沉积、肝星状细胞(HSCs)激活、胶原交联和炎症反应。肝纤维化的异质性是肝内微环境异质性以及纤维化相关酶和细胞异质性表达共同作用的结果,这使得肝纤维化进展机制的研究变得复杂。这种异质性在细胞与基质间的相互作用以及纤维化过程中的作用值得探索。在本文中,我们将描述肝纤维化过程中肝脏基质和肝内细胞异质性的现象和机制,并讨论异质性因素在纤维化发展中的相互作用。阐明异质性对于更深入理解肝纤维化的病理机制以及临床诊断和靶向治疗都很重要。