Puri Munish, Sonawane Snehal
Onco-Immunology, Magnit Global, Folsom, CA 95630, USA.
Department of Pathology, University of Illinois, Chicago, IL 60612, USA.
Int J Mol Sci. 2025 Apr 23;26(9):3988. doi: 10.3390/ijms26093988.
Liver Sinusoidal Endothelial Cells (LSECs) play a crucial role in maintaining liver homeostasis, regulating immune responses, and fibrosis in liver diseases. This review explores the unique functions of LSECs in liver pathology, particularly their roles in immune tolerance, antigen presentation, and the modulation of hepatic stellate cells (HSCs) during fibrosis. LSECs act as key regulators of immune balance in the liver by preventing excessive immune activation while also filtering antigens and interacting with immune cells, including Kupffer cells and T cells. Metabolic Dysfunction-Associated Fatty Liver Disease(MAFLD) is significant because it can lead to advanced liver dysfunction, such as cirrhosis and liver cancer. The prevalence of Metabolic Associated Steatohepatitis (MASH) is increasing globally, particularly in the United States, and is closely linked to rising rates of obesity and type 2 diabetes. Early diagnosis and intervention are vital to prevent severe outcomes, highlighting the importance of studying LSECs in liver disease. However, during chronic liver diseases, LSECs undergo dysfunction, leading to their capillarization, loss of fenestrations, and promotion of pro-fibrotic signaling pathways such as Transforming growth factor-beta (TGF-β), which subsequently activates HSCs and contributes to the progression of liver fibrosis. The review also discusses the dynamic interaction between LSECs, HSCs, and other hepatic cells during the progression of liver diseases, emphasizing how changes in LSEC phenotype contribute to liver scarring and fibrosis. Furthermore, it highlights the potential of LSECs as therapeutic targets for modulating immune responses and preventing fibrosis in liver diseases. By restoring LSECs' function and targeting pathways associated with their dysfunction, novel therapies could be developed to halt or reverse liver disease progression. The findings of this review reinforce the importance of LSECs in liver pathology and suggest that they hold significant promises as targets for future treatment strategies aimed at addressing chronic liver diseases.
肝窦内皮细胞(LSECs)在维持肝脏内环境稳定、调节免疫反应以及肝脏疾病的纤维化过程中发挥着关键作用。本综述探讨了LSECs在肝脏病理学中的独特功能,特别是它们在免疫耐受、抗原呈递以及纤维化过程中对肝星状细胞(HSCs)的调节作用。LSECs通过防止过度免疫激活,同时过滤抗原并与免疫细胞(包括库普弗细胞和T细胞)相互作用,从而成为肝脏免疫平衡的关键调节因子。代谢功能障碍相关脂肪性肝病(MAFLD)很重要,因为它会导致晚期肝功能障碍,如肝硬化和肝癌。代谢相关脂肪性肝炎(MASH)的患病率在全球范围内呈上升趋势,尤其是在美国,并且与肥胖率和2型糖尿病的上升密切相关。早期诊断和干预对于预防严重后果至关重要,这凸显了研究LSECs在肝脏疾病中的重要性。然而,在慢性肝病期间,LSECs会发生功能障碍,导致其毛细血管化、窗孔丧失,并促进促纤维化信号通路,如转化生长因子-β(TGF-β),随后激活HSCs并促进肝纤维化的进展。该综述还讨论了在肝脏疾病进展过程中LSECs、HSCs和其他肝细胞之间的动态相互作用,强调了LSEC表型变化如何导致肝脏瘢痕形成和纤维化。此外,它强调了LSECs作为调节免疫反应和预防肝脏疾病纤维化的治疗靶点的潜力。通过恢复LSECs的功能并靶向与其功能障碍相关的途径,可以开发新的疗法来阻止或逆转肝脏疾病的进展。本综述的研究结果强化了LSECs在肝脏病理学中的重要性,并表明它们作为未来旨在治疗慢性肝病的治疗策略靶点具有巨大潜力。