Liver regeneration in acute severe liver impairment: a clinicopathological correlation study

祖细胞 肝细胞 病理 肝再生 肝移植 肝病 间质细胞 肝损伤 薄壁组织 生物 再生(生物学) H&E染色 移植 免疫组织化学 肝星状细胞 干细胞 医学 内科学 细胞生物学 内分泌学 体外 生物化学
作者
Aezam Katoonizadeh,Frederik Nevens,Chris Verslype,Jacques Pirenne,Tania Roskams
出处
期刊:Liver International [Wiley]
卷期号:26 (10): 1225-1233 被引量:159
标识
DOI:10.1111/j.1478-3231.2006.01377.x
摘要

Although normally quiescent, the adult mammalian liver possesses a great capacity to regenerate after different types of injury. Major players in the regeneration process are mature residual cells, including hepatocytes, cholangiocytes and stromal cells. However, if the regenerative capacity of mature cells is impaired, hepatic progenitor cells (HPCs) are activated and expand into the liver parenchyma. Upon transit amplification, the progenitor cells generate new hepatocytes and biliary cells to restore liver homeostasis.To study the relationship between different histopathological parameters as well as their correlations with clinical parameters and outcome, we examined liver specimens from 74 patients with acute or subacute severe liver impairment by immunohistochemistry for CK7/CK19 (evaluation of HPCs activation/differentiation), Mib1(Ki 67)/P21 (evaluation of proliferative activity/proliferation arrest of hepatocytes) and hematoxylin and eosin (evaluation of hepatocyte loss).Of the 74 patients, 32% survived without transplantation, 14% died without transplantation and 54% were transplanted. Our results show that a threshold of 50% loss of hepatocytes, associated with significant decrease in the proliferative activity of remaining mature hepatocytes, is needed for extensive hepatic progenitor cell activation. Such activation is a sign of disease severity and occurs early (within 1 week) in the disease course. However, development of intermediate hepatocytes, suggesting HPCs differentiation towards mature hepatocytes, takes at least 1 week's time. We found a positive correlation between histopathological parameters (percentage hepatocyte loss, number of proliferating hepatocytes and number of HPCs) and clinical parameters of liver impairment such as model for end stage liver diseases (MELD). Surviving patients compared with those who either died or were transplanted had significantly less hepatocyte loss, less HPCs activation and more mature hepatocyte proliferative activity. Hepatocyte proliferative activity and degree of hepatocyte loss were the most important independent histopathological parameters in predicting outcome.Liver biopsy can provide important additional information in a patient with severe acute liver impairment.

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