The regenerating liver

The liver has a high capacity for regeneration following injury; however, there is debate about which hepatic cell populations contribute to this process. Hepatocytes, which are the predominant cell type in the liver, mediate regeneration in response to many types of damage, yet the liver is able to recover even when hepatocyte proliferation is inhibited. Hepatic stellate cells (HSCs) are a collagen-producing cell population in the liver that is associated with fibrosis, and these cells also exhibit mesenchymal stem cell-like properties, suggesting that HSCs cells could function as a liver-resident stem cell population. Claus Kordes and colleagues at Heinrich Heine University investigated the contribution of HSCs to liver regeneration. HSCs were isolated from GFP-expressing rats and transplanted into wild type animals that had undergone partial hepatectomy in the presence of toxic substances, which suppress hepatocyte proliferation. Transplanted HSCs engrafted in bone marrow and homed to the injured liver. Within the liver, HSCs differentiated into mesenchymal and epithelial cells, including cholangiocytes and hepatocytes, by transiently serving as hepatic progenitor cells. In an accompanying commentary, Christopher Hindley, Gianmarco Mastrogiovanni, and Meritxell Huch discuss how these findings alter the current understanding of HSCs and liver regeneration. The accompanying super-resolution microscopy image shows desmin immunofluorescence (green), indicative of HSCs, within K19+ cells (red) within the center of duct-like structures following liver injury. This staining profile indicates that intermediate states of mesenchymal and epithelial cells exist in the putative progenitor cells of the liver

Published November 17, 2014, by Corinne Williams

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Category: Research Article

Hepatic stellate cells contribute to progenitor cells and liver regeneration

Abstract

Retinoid-storing hepatic stellate cells (HSCs) have recently been described as a liver-resident mesenchymal stem cell (MSC) population; however, it is not clear whether these cells contribute to liver regeneration or serve as a progenitor cell population with hepatobiliary characteristics. Here, we purified HSCs with retinoid-dependent fluorescence-activated cell sorting from eGFP-expressing rats and transplanted these GFP+ HSCs into wild-type (WT) rats that had undergone partial hepatectomy in the presence of 2-acetylaminofluorene (2AAF) or retrorsine, both of which are injury models that favor stem cell–based liver repair. Transplanted HSCs contributed to liver regeneration in host animals by forming mesenchymal tissue, progenitor cells, hepatocytes, and cholangiocytes and elevated direct bilirubin levels in blood sera of GUNN rats, indicating recovery from the hepatic bilirubin–handling defect in these animals. Transplanted HSCs engrafted within the bone marrow (BM) of host animals, and HSC-derived cells were isolated from BM and successfully retransplanted into new hosts with injured liver. Cultured HSCs transiently adopted an expression profile similar to that of progenitor cells during differentiation into bile acid–synthesizing and –transporting hepatocytes, suggesting that stellate cells represent a source of liver progenitor cells. This concept connects seemingly contradictory studies that favor either progenitor cells or MSCs as important players in stem cell–based liver regeneration.

Authors

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The plastic liver: differentiated cells, stem cells, every cell?
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Category: Commentary

The plastic liver: differentiated cells, stem cells, every cell?

Abstract

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