- Open Access
Age-dependent development of liver fibrosis in Glmp gt/gt mice
Fibrogenesis & Tissue Repair volume 9, Article number: 5 (2016)
Mice lacking glycosylated lysosomal membrane protein (Glmp gt/gt mice) have liver fibrosis as the predominant phenotype due to chronic liver injury. The Glmp gt/gt mice grow and reproduce at the same rate as their wild-type siblings. Life expectancy is around 18 months.
Wild-type and Glmp gt/gt mice were studied between 1 week and 18 months of age. Livers were analyzed using histological, immunohistochemical, biochemical, and qPCR analyses.
It was shown that Glmp gt/gt mice were not born with liver injury; however, it appeared shortly after birth as indicated by excess collagen expression, deposition of fibrous collagen in the periportal areas, and increased levels of hydroxyproline in Glmp gt/gt liver. Liver functional tests indicated a chronic, mild liver injury. Markers of inflammation, fibrosis, apoptosis, and modulation of extracellular matrix increased from an early age, peaking around 4 months of age and followed by attenuation of these signals. To compensate for loss of hepatocytes, the oval cell compartment was activated, with the highest activity of the oval cells detected at 3 months of age, suggesting insufficient hepatocyte proliferation in Glmp gt/gt mice around this age. Although constant proliferation of hepatocytes and oval cells maintained adequate hepatic function in Glmp gt/gt mice, it also resulted in a higher frequency of liver tumors in older animals.
The Glmp gt/gt mouse is proposed as a model for slowly progressing liver fibrosis and possibly as a model for a yet undescribed human lysosomal disorder.
Mammalian liver plays a vital role in the maintenance of body homeostasis. This homeostatic activity comprises the supply of energy substances and a number of blood components for which the liver is the only or major site of synthesis, i.e., serum albumin . In addition, the liver removes a wide selection of potentially harmful substances arriving from the gut via the portal vein as well as substances, which are needed for synthetic purposes. Clearance from the circulatory system of various macromolecules and particles occurs by endocytosis, generally leading to degradation of endocytosed substances in the lysosomes followed by excretion or recycling of the degradation products in synthetic pathways. The liver is one of the most active metabolic organs of the body, having a high turnover of its constituents. Degradation of intracellular substances proceeds via the autophagic pathway for which the lysosome is also the endpoint .
Proper functioning of the lysosomes is essential to the homeostatic activity of hepatocytes and often also to their survival . A heterogeneous group of more than 50 congenital metabolic disorders characterized by the lack or dysfunction of a protein within the endo-lysosomal pathway has been described and categorized as lysosomal disorders [4–11]. Most of these proteins are degradative enzymes or membrane proteins [10, 11]. These lysosomal disorders have widely varying phenotypes; however, symptoms are often observed in tissues with low proliferation capacity, such as the brain, or in cell types with a high substrate turnover such as hepatocytes [7, 8, 12, 13]. A consequence of lysosomal disorder is gradual accumulation of undegraded or unrecycled substances leading to increasing pathogenic effects at the cellular and organ level eventually leading to systemic dysfunction [14, 15]. Depending on the type and degree of such a lysosomal disorder, patients are faced with a shorter life expectancy [7, 8].
A frequent clinical manifestation in many lysosomal disorders is liver fibrosis , a consistent result of almost every type of prolonged or chronic liver injury . Fibrogenesis is characterized by hepatocyte apoptosis/necrosis and activation of Kupffer cells and hepatic stellate cells [16–19]. These events lead to release of a wide array of cytokines (e.g., TGF-β, TNF-α, and PDGF), leading to infiltration of leukocytes and further activation of stellate cells [17, 20, 21]. A state of inflammation results, often accompanied with oxidative stress [17, 20, 21].
Fibrosis is a wound healing process during which the balance between the extracellular matrix components is shifted partly due to changes in expression of matrix genes, such as collagen I, and partly due to changes in expression of an array of matrix degrading enzymes and their inhibitors, leading to accumulation of stiff, highly cross-linked filamentous collagen structures [20, 22, 23]. If untreated, liver fibrosis may proceed to liver cirrhosis, cancer, liver failure, and eventually death . Worldwide chronic liver injury is one of the major causes of morbidity and mortality .
The progression from chronic liver injury to liver fibrosis and eventually cirrhosis depends on the etiology [17, 19]. Having access to animal models representing these different pathologies is important in order to lay the foundation for appropriate treatment strategies. Mouse models representing spontaneous liver fibrosis starting early in life but with a slow progression are scarce [26, 27]. We recently reported the successful generation of a mouse model lacking expression of the glycosylated lysosomal membrane protein (GLMP) . The physiological function of this protein is unclarified, yet it appears to be essential to a healthy liver. By the age of 6 months, the Glmp gt/gt mouse had developed a marked liver fibrosis associated with hepatic cell death, oxidative stress, active fibrogenesis, and activation of liver progenitor cells .
The present study was undertaken to explore the age-dependent development of liver fibrosis in Glmp gt/gt mice. This report shows that development of liver fibrosis is initiated shortly after birth in Glmp gt/gt mice and progresses to a peak around 4 months of age. These mice are long-lived but develop liver tumors at later stages in life. Expression of inflammation markers and genes responsible for alteration of the extracellular matrix increases from 2 weeks of age. Activation of hepatic stellate cells and hepatic progenitor cells is especially prominent around 3 to 4 months of age. Further, expression of genes for inhibitors of cell cycle progression is increased. At the age of 18 months, a majority of the Glmp gt/gt mice had developed liver tumors. We propose that the Glmp gt/gt mouse model may prove to be very useful for studies of slowly progressing liver fibrosis and possibly as a model for a yet undescribed lysosomal disorder.
Animals and handling
All animal experiments were reviewed and approved by the Norwegian Animal Research Authority and performed according to national laws and regulations. Generation of wild-type (WT) and Glmp gt/gt mice has been described . The animals were housed in an approved animal facility with access to standard rodent chow and water ad libitum unless otherwise stated. Biological samples from both males and females were collected at designated age-points (newborn—18 months). Samples not immediately processed or used for analyses were snap-frozen in liquid N2 and stored at −80 °C until use.
Serum and hematological analysis
Blood was collected by cardiac puncture, coagulated at room temperature before centrifugation at 1500g for 20 min. Serum was collected and immediately analyzed for serum alanine transaminase , aspartate transaminase (AST), γ-glutamyl-transferase, bile acid, bilirubin, and albumin concentrations at The Central Laboratory, Department of Basic Sciences and Aquatic Medicine, Norwegian School of Veterinary Science. Serum levels of TGF-β were assessed using enzyme-linked immunosorbent assay (#MB100B, R&D systems, Minneapolis, MN, USA) according to manufacturer’s procedure.
Blood was collected from 4.5-month-old male WT and Glmp gt/gt mice by cardiac puncture into micro-vessel EDTA tubes (Terumo Europe, Leuven, Belgium). Hematological analyses were performed by The Central Laboratory, Department of Basic Sciences and Aquatic Medicine, Norwegian School of Veterinary Science.
Mouse tissues were fixed in 10 % neutral buffered formalin overnight, processed into paraffin blocks, and sectioned into 4-μm-thick slices. Liver sections were stained with either hematoxilin and eosin (H&E) or acid fuchsin orange G (AFOG) according to standard techniques.
Formalin-fixed paraffin-embedded sections were deparaffinized in xylene, rehydrated in a graded series of ethanol, and demasked in a microwave oven for 24 min in Tris/EDTA (TE) buffer (pH = 9.1). Antibodies for immunohistochemistry were Rabbit monoclonal anti-Ki67 (1:500, SP6, GTX16667, Cytotech ApS, Hellebæk, Denmark). Sections were counterstained with hematoxylin, and the antigen-antibody reaction was visualized with Dako EnVision horse radish peroxidase system using 3,3′-diaminobenzidine as the chromogen (K4007, DAKO North America Inc., Camarillo, CA, USA).
Livers from four individual animals of each genotype and age group were used for quantification of proliferating hepatocytes. From each animal, two representative liver tissue blocks were used for obtaining four randomly collected slices including at least 1000 hepatocytes from each liver (imaged with ×40 obj.). The total number of proliferative hepatocytes, given as the sum of all positively Ki67 labeled hepatocyte nuclei, and the semi-quantitative estimation of the average number of hepatocyte nuclei included in a magnification field were determined by counting.
Immunofluorescence was performed as described previously . Antibodies used for immunofluorescence were Rat monoclonal anti-A6 (cell culture supernatant 1:25) kindly provided by Dr. Valentina Factor  as primary antibody and Alexa-Fluor-633 as secondary antibody (Molecular Probes, Eugene, OR, USA), and sections were counterstained with DAPI. Estimation of immunofluorescence intensity was graded in a semi-quantitative summary.
Transmission electron microscopy
Mice (n = 3, age 6 months) were subjected to perfusion fixation using HEPES buffer (0.1 M, pH 7.2–7.4) with 4 % formaldehyde and 2.5 % glutaraldehyde. Tissues were collected, cut into blocks of 1 mm3, transferred to new fixative solution, and kept at 4 °C overnight. The samples were rinsed 2 × 10 min in 0.1 M sodium cacodylate buffer prior to post-fixation (2 % OsO4 in 0.1 M sodium cacodylate buffer) for 1 h, and rinsed 5 × 10 min in distilled water before bulk staining with 1.5 % uranyl acetate (CH3COO)2UO2·2H2O)  in distilled water for 30 min in the dark. Fixed tissue samples were dehydrated in a graded series of ethanol for 10 min each (70, 80, 90, 96 %), 4 × 15 min in 100 % ethanol and finally 2 × 10 min in propylene oxide. Following dehydration, tissue samples were infiltrated with epoxy:propylene oxide (1:1) for 30–60 min on a rotary shaker, evaporated overnight, and the following day incubated 1 h in pure epoxy before embedding in plastic capsules and polymerization at 60 °C. Five tissue blocks were selected per individual mouse. Ultrathin sections were obtained using a Leica Ultracut S microtome (Leica, Wetzlar, Germany) with diamond knife and collected on copper-coated grids before staining with lead citrate for 20 s. All electron micrographs were obtained with a CM100 transmission microscope (Philips, Amsterdam, The Netherlands) at 80 kV.
Determination of Hydroxyproline
Briefly, frozen livers from WT and Glmp gt/gt mice were ground into powder, hydrolyzed in 6 M hydrochloric acid (HCl) at 100 °C o/n followed by centrifugation at 13,000g for 10 min. Supernatants were diluted 1:2 with 4 M HCl. Liver hydroxyproline contents were determined using Hydroxyproline Assay kit (#QZBhypro2, QuickZyme Biosciences, Leiden, The Netherlands), according to manufacturer’s protocol.
Gene expression analyses
RNA extractions from mouse liver were carried out according to the manufacturer using RNeasy Plus kit (Qiagen, Hilden, Germany). The expression of selected messenger RNA (mRNA) transcripts (Additional file 1: Table S1) was analyzed by quantitave PCR (qPCR) using a LightCycler 480 (Roche Diagnostics, Manheim, Germany) and LightCycler® 480 SYBR Green I Master Mix (Roche Applied Science). PCR efficiencies were experimentally determined for each primer pair. Relative gene expression was calculated using the ΔΔCt-method, with beta-actin and eukaryotic translation elongation factor 2 as reference genes.
All results are expressed as mean ± s.e.m. All data were analyzed using two-tailed t test (SigmaPlot™ , Systat Software Inc, Chicago, IL, US) unless otherwise stated.
Chronic liver inflammation is initiated shortly after birth in Glmp gt/gt mice
As a background for evaluating the lack of GLMP expression on liver health, we measured the mRNA levels for Glmp from birth till 9 months of age. Figure 1a shows a rapid increase in Glmp expression within the first week of life, reaching the adult levels by week 2. Next, livers from wild-type (WT) and Glmp gt/gt mice were analyzed macroscopically and histologically. Figure 1b shows representative liver macro images. No signs of liver injury were observed in newborn mice (data not shown), nor did livers from 1 week old Glmp gt/gt mice show obvious signs of liver injury. At 1 month of age, however, subcapsular bleeding was observed (Fig. 1b). From the age of 3 months increasing subcapsular contractions appeared, giving a nodular appearance of Glmp gt/gt livers (Fig. 1b). By the age of 6 months, more distinct nodules were seen; however, at 9 months, the contracted liver surface appeared slightly smoothened compared to 3 and 6 months old Glmp gt/gt livers (Fig. 1b). Histological examination revealed infiltration of leukocytes as early as 1 week after birth in Glmp gt/gt livers (Fig. 1c), followed by an increased number of infiltrating inflammatory cells as the animals grew older. A pronounced distortion of the hepatic parenchymal architecture was observed from 1 month of age (Fig. 1c). In addition, the Glmp gt/gt livers were characterized by wide spread extramedullar hematopoietic cells from the age of 1 week to the age of 6 months (Fig. 1c). Very moderate amounts of such hematological precursors were only seen in 1 week old WT livers as is typical for young individuals .
Expression of genes involved in inflammation and recruitment of inflammatory cells in newborn Glmp gt/gt mice was similar to that of WT confirming the observed absence of liver injury in newborn Glmp gt/gt mice. In support of histological analyses mRNA levels for the inflammation marker S100 calcium-binding protein A8 (S100a8) and its interacting partner S100a9, both ligands of the Receptor for advanced glycation end-products (RAGE receptor)  were markedly elevated in Glmp gt/gt livers from 1 week of age (Fig. 2a,b). The expression of mRNA for Tnfa (Tumor necrosis factor alpha) also increased but did not reach statistical significance until 1 month of age in Glmp gt/gt livers (Fig. 2c). A substantial increase in the expression levels of these three genes was detected in Glmp gt/gt livers compared to WT, reaching an apparent peak at 3.5–4.5 months of age followed by reduced expression (Fig. 2a–c). The mRNA expression of a sensor of damage-associated molecular patterns, high-mobility group box 1 (HMGB1), also a ligand of the RAGE receptor , showed a slower increase with age peaking at 6 months of age and remaining elevated throughout the observation period (Fig. 2d).
Histological and transmission electron microscopy (TEM) analyses of other organs showed no abnormalities in Glmp gt/gt mice (Additional file 2: Figure S1).
Reduced liver function in Glmp gt/gt mice
The apparent decrease in expression of inflammatory marker genes after 3.5–4.5 months of age in Glmp gt/gt livers were compared to liver functional analyses. In Glmp gt/gt mice, modest but significantly elevated levels of serum alanine transaminase  (Fig. 2e) and aspartate transaminase (AST) were detected between 3.5 and 12 months of age (Fig. 2f), indicating hepatocyte damage. The relative differences between genotypes were stable with age (Fig. 2e, f). The serum bile acid levels were markedly elevated in Glmp gt/gt mice compared to WT at all ages studied (Fig. 2g), whereas serum albumin, a marker for hepatic function and the general status of animal health , was reduced in Glmp gt/gt mice compared to WT at all ages studied (Fig. 2h). Serum levels of γ-glutamyl-transferase and serum bilirubin levels remained normal in Glmp gt/gt mice (data not shown).
Glmp gt/gt mice have anemia, thrombocytopenia, and reduced levels of white blood cells
A complete blood analysis was performed on 4.5-month-old WT and Glmp gt/gt mice. A decrease in concentration of red blood cells (RBC), hemoglobin (HGB), and hematocrit (HCT) and increase in the range of cellular sizes of erythroid cells (RDW) in Glmp gt/gt mice were observed indicating anemia (Table 1). Furthermore, decreased platelet (PLT) concentration in Glmp gt/gt mice was detected (Table 1) as well as extended bleeding time (data not shown). The low platelet count was in accordance with the decreased serum levels of TGF-β in Glmp gt/gt mice, aged 3 weeks–15 months (Additional file 3: Figure S2). In support of the observed increase in infiltrating inflammatory cells in the Glmp gt/gt liver, a significantly reduction in the levels of circulating white blood cells (WBC) was observed in these mice compared to WT mice (Table 1).
Liver fibrosis is initiated after birth in Glmp gt/gt mice
Staining of liver sections with AFOG showed no increase in collagen staining in Glmp gt/gt livers compared to WT at 1 week of age (Fig. 3a). However, from 1 month of age, excess collagen was clearly visible in the parenchyma of Glmp gt/gt livers (Fig. 3a). Liver hydroxyproline levels were quantified as a measure of excess collagen in Glmp gt/gt livers. Figure 3b shows that in newborn Glmp gt/gt mice the levels of hydroxyproline did not differ from those of WT mice, demonstrating that Glmp gt/gt mice were not born with liver fibrosis. Elevated hydroxyproline contents were detected in Glmp gt/gt livers from 2 weeks, indicating that fibrogenesis had been initiated by this age (Fig. 3b). The highest levels of hydroxyproline were detected in 4.5-month-old Glmp gt/gt livers, reaching on average a threefold increase compared to WT (Fig. 3b). In accordance with the observed attenuation of inflammation in Glmp gt/gt livers after 4.5 months (Figs. 1 and 2), the hydroxyproline levels were reduced somewhat after this age (Fig. 3b).
Gene expression analyses of TGF-β (Fig. 4a), an inducer of fibrogenesis, α-SMA (Fig. 4b), marker of activated hepatic stellate cells, and proteins involved in matrix remodeling collagen 1A1 (COL1A1), matrix metalloproteinase-2 and 9 (MMP2, MMP9) and tissue inhibitor of metalloproteinase-1 (TIMP1) (Fig. 4c–f) revealed an increase in expression peaking at 3.5–4.5 months of age in Glmp gt/gt livers, where all markers were significantly increased compared to WT. As with the inflammatory markers (Fig. 2a–d) and collagen contents (Fig. 3a, b), the relative differences between the genotypes was reduced after this age (Fig. 4).
Simultaneous loss and proliferation of hepatocytes in Glmp gt/gt mice
An increased apoptotic activity has been demonstrated in liver from Glmp gt/gt mice . To explore the regenerative capacity of WT and Glmp gt/gt livers, paraffin-embedded liver sections were labeled for the proliferation marker Ki67 . Fig. 5a, b shows that the number of proliferating cells is highly increased in 1-month-old Glmp gt/gt livers compared to WT. A similar tendency, although not as pronounced was observed in 3 and 6 months old mice (Fig. 5b). At 9 months of age, the number of proliferating hepatocytes was comparable between the genotypes (Fig. 5a, b). Semi-quantitative estimation of the total hepatocyte number included in a microscopic field (×40 obj.) showed comparable cell numbers at 1 month of age (Fig. 5c). In Glmp gt/gt livers from 3- and 6-month-old mice, the number of hepatocytes was lower compared to WT due to enlarged size (Fig. 5c). However, at 9 months of age, Glmp gt/gt mice appeared to have normalized the number of hepatocytes (Fig. 5c).
To further investigate the proliferative status, the relative expression of Cyclin D1 (CCND1), a key regulator of cell cycle progression , was determined. Figure 5d shows an increase in Ccnd1 expression at 1 month of age in Glmp gt/gt livers compared to WT, followed by an expression peak at 3.5 months and a reduction in relative gene expression after this age. The expression of Cyclin-dependent kinase inhibitor 2A (Cdkn2a), an inhibitor of CCND1, the upregulation of which promotes senescence and growth arrest , was significantly upregulated in Glmp gt/gt livers compared to WT at 1 week of age (Fig. 5e). Similar to the expression of Ccnd1, and the other genes involved in inflammation and fibrogenesis, the difference in relative Cdkn2a gene expression peaked at 3.5 months followed by a reduction after this age (Fig. 5e). At the peak age of 3.5 months, gene expression analyses of Cysteine-rich angiogenic inducer 61 (Cyr61), a marker for senescent cells, showed a significant upregulation in Glmp gt/gt livers compared to WT (Fig. 5f).
Oval cell expansion in Glmp gt/gt livers
The age-dependent activation of the hepatic oval cell compartment was studied by immunofluorescence staining for the specific marker, A6 . Figure 6 shows similar staining in Glmp gt/gt and WT livers at 1 month of age. However, at 3 months, a strong increase in A6 staining was detected in Glmp gt/gt livers, followed by a gradual decrease at 6 and 9 months of age, where the labeling is only slightly increased in Glmp gt/gt livers compared to WT (Fig. 6).
Liver tumors develop in old Glmp gt/gt mice
Systematic evaluation of livers from Glmp gt/gt mice aged between 12 and 18 months, revealed an increased frequency of liver tumors compared to WT mice (Table 2). Additional file 4: Figure S3 shows representative liver macro images from 18 months old Glmp gt/gt and WT mice. Hepatocellular tumors (Additional file 4: Figure S3A, B) and hemangioma-like tumors with dilated vessels were detected in the majority of Glmp gt/gt livers (Additional file 4: Figure S3A,C). In spite of tumor growth, the average liver/body weight ratio was only slightly increased in 18 months old Glmp gt/gt mice, and no significant differences were detected for spleen/body weight ratio (data not shown). The life expectancy of the Glmp gt/gt mice appeared to be around 18 months, as the mortality rate of Glmp gt/gt mice increased between 16 and 18 months of age (data not shown). Liver functional tests, assessed by measuring serum parameters, suggested that liver function in old Glmp gt/gt mice was comparable to Glmp gt/gt mice of younger age (Additional file 5: Figure S4 A, B, C, D). Similarly, total liver collagen in Glmp gt/gt livers did not correlate with increasing incidence of tumor growth (Additional file 6: Figure S5).
In this report, the progression of chronic liver injury in Glmp gt/gt mice across the expected life span is described. In newborn Glmp gt/gt mice, no signs of liver injury were detected, but chronic liver injury was initiated shortly after birth. At 1 month of age signs of liver damage appeared in the form of subcapsular bleeding, infiltration of inflammatory cells and increased levels of hydroxyproline. Histological analyses detected increased deposition of fibrous collagen in the periportal areas of Glmp gt/gt liver in accordance with the increased levels of hydroxyproline and increased expression of α-smooth muscle actin (α-SMA) due to activation of stellate cells, the major producers of extracellular matrix components in both healthy and fibrotic liver . The increased presence of inflammatory cells coincided with increased expression levels of mRNA for inflammatory markers and cytokines, matrix modulating enzymes, and their inhibitors. A similar expression pattern for Ccnd1 and Cdkn2a were observed. Further, liver injury was reflected in the elevated serum transaminase levels, mild anemia, increased hepatocyte proliferation, and oval cell activation. Finally, a majority of Glmp gt/gt mice developed liver cancers after the age of 12 months.
In wild-type mice Glmp expression increased rapidly after birth, coinciding with the rapid growth of both liver and the animal. In a recent report, we showed that the liver/body weight ratio more than doubled in the first 2 weeks of life . In the early phase of life, the liver metabolism has to adapt to lactation and in this scenario, the lack of GLMP presumably causes the chronic liver injury leading to the observed fibrosis. In a previous report, we showed increased apoptosis and oxidative stress in Glmp gt/gt livers leading to hepatocyte loss . Such a loss may be compensated by proliferation of differentiated hepatocytes or by oval cell proliferation and transdifferentiation into hepatocytes. The former typically occurs after mild or limited injuries to the liver by for instance carbon tretrachloride (CCl4) . However, in situations of persistent or severe injury leading to insufficient hepatocyte proliferation, oval cells are mobilized to replace lost hepatocytes or to complement an inadequate rate hepatocyte of regeneration [40–43]. Increased hepatocyte proliferation and oval cell mobilization were observed in this study up to the age of 6 months, indicating that lack of GLMP resulted in persistent liver injury. Several rodent models with chronic metabolic liver injuries are associated with proliferation of oval cells in order to compensate for impaired hepatocyte proliferation [42–45]. After 6 months, the oval cell activation declined, and the hepatocyte proliferation appeared to be normalized in Glmp gt/gt livers compared to WT. The liver injury and fibrosis, however, had not been reversed as shown by the continued increase in the levels of hydroxyproline and HMGB1. The observed continued elevated levels of serum transaminases, increased bile acids and lower serum albumin, often associated with chronic liver disease also supported the notion of continued liver injury [46–48]. Proliferation of liver cells was concomitant with the observed changes in gene expression of the regulator of cell cycle progression, CCND1 and its inhibitor CDKN2A, which increased shortly after birth, reaching a peak around 3.5 months and followed by a decline to normal levels at 9 months. The effect on cell cycle regulation and increased expression of Cyr61 at 3.5 months indicated cell senescence and initiation of a repair process . The combined effect of these regulators on cell proliferation may be to ensure that activated stellate cells are silenced and damaged cells especially damaged hepatocytes are removed. The increased expression of Cyr61 indicated that regeneration of the liver is activated and may be the reason for avoiding progression to severe cirrhosis, liver failure, and early death . Using microarray analyses of the Mdr2 −/− mouse model for chronic biliary injury . Katzenellenbogen et al. showed that DNA replication appeared normal in Mdr2 −/− liver, while cell division was inhibited, possibly as a protective mechanism from uncontrolled proliferation . At 9 months of age, we detected comparable levels of Ki67 staining and numbers of hepatocytes in Glmp gt/gt and WT livers, suggesting establishment of a new balance between hepatocyte death and replenishment. Activation of oval cells appeared to be important for maintenance of liver function in Glmp gt/gt mice. However, oval cells have also been shown to contribute to the development of liver cancer [50, 51], a common end-stage in chronic liver disease [19, 24, 52]. Even though liver functional tests indicated only a mild liver injury and adequate hepatic function in old Glmp gt/gt mice, the prolonged insult eventually promoted tumorigenesis in about 60 % of 18-month-old mice. A recent study has questioned the true contribution of oval cell expansion in the hepatocyte repopulation after liver injury ; however, our data showed that the oval cell compartment was activated at the age where the highest expression of the cell cycle inhibitor CDKN2A was detected  and that the total number of hepatocytes normalized after oval cell activation. Further studies will be required to elucidate the role of the oval cells in Glmp gt/gt liver.
In our first characterization of the Glmp gt/gt mice, we reported accumulation of lipofuscin and iron in storage vacuoles in Glmp gt/gt Kupffer cells . Here, we show that the Glmp gt/gt livers were exposed to chronic inflammation right after birth. Further, we detected mild anemia in Glmp gt/gt mice, consistent with anemia of inflammation [54, 55]. A study conducted by Nelson et al.  showed that iron deposition specifically in Kupffer cells was associated with metabolic liver injury. In a recent study, we have demonstrated dysregulation of glucose and lipid metabolism in Glmp gt/gt liver and isolated primary hepatocytes . The absence of signs of liver injury in newborn Glmp gt/gt mice suggests that GLMP may not be essential in mouse prenatal life. At the mRNA level, Glmp expression has been shown in mouse embryos , suggesting that GLMP might have a role in a biological pathway not active until birth. Dramatic changes in the hepatic gene expression pattern take place right after birth in mice, switching from primarily hematopoietic pathways to metabolic pathways . A disturbed lipid metabolism is a very likely generator of reactive oxygen species (ROS), which are powerful inducers of fibrosis . Lipopolysaccharides (LPSs) leaked from the intestine represent an additional contribution to the development of liver fibrosis by causing inflammation [59–61].
An interesting question is why fibrosis occurs in Glmp gt/gt liver, and yet it appears to reach a new equilibrium after 6 months, albeit with a high risk of tumor development in old animals. Based on the data presented here showing that hepatocyte proliferation and oval cell proliferation occur simultaneously, we hypothesize that four factors may contribute to the observed fibrosis: the demand for high activity in metabolic pathways after birth, increased influx of LPS from the intestine, the demand for liver growth to accompany the growth of the animal, and the increased need to replace damaged hepatocytes. The high demand for metabolic activity, especially with regard to lipids, which occurs after birth, generates ROS and oxidative stress in Glmp gt/gt hepatocytes due to their reduced lipid metabolic capacity . This impairs their proliferation potential and leads to apoptosis and influx of inflammatory cells from circulation [17, 19, 20]. Further, in the first 4–5 months the liver has to increase its size to meet the requirements of the growing animal. Simultaneously, increased influx of LPS, secondary to chronic liver injury, is carried via the portal circulation to liver [62–64]. Kupffer cells can be activated by LPS  or through ingestion of hepatocyte apoptotic bodies , leading to secretion of pro-inflammatory and pro-fibrogenic cytokines like TNF-α [66, 67] and TGF-β [29, 68]. These cytokines are key activators of oval cells and hepatic stellate cells, respectively, in chronically injured liver [17, 20, 69]. In addition, LPS can directly promote stellate cell activation through toll-like receptor 4 (TLR4) . During the growth phase, expansion of the oval cell compartment is required in Glmp gt/gt liver in order to meet the demand for replenishment of damaged hepatocytes and proliferation for hyperplastic growth. However, around 6 months of age the mice have reached their full body size and so has the liver. When the demand for hyperplastic liver growth is no longer relevant, the Glmp gt/gt liver appears less dependent on oval cell expansion in maintaining adequate liver function.
In summary, we have presented the entire liver disease development in Glmp gt/gt mice, from initiation, progression, and compensation to tumor development over a life span of 18 months. To our knowledge, this is the first in-depth characterization of liver disease development in a transgenic mouse model for a spontaneous, slowly progressing liver fibrosis. We show that liver injury is initiated right after birth in Glmp gt/gt mice. The injury is mild, but an imbalance between hepatocyte death and proliferation activates the oval cell compartment by the age of 3 months. A new balance between hepatocyte loss and replacement appears to be reached by the age of 9 months; however, the continuous proliferation eventually results in tumorigenesis in Glmp gt/gt livers. Finally, based on our earlier data, we suggest that metabolic liver injury may be the cause of the liver disease in Glmp gt/gt mice and propose that this Glmp gt/gt mouse model may become useful for studies of slowly progressing liver fibrosis and possibly as a model for a yet undescribed lysosomal disorder.
alpha- smooth muscle actin
antigen marker for hepatic oval cells
acid fuchsin orange G
cyclin-dependent kinase inhibitor 2A
cysteine-rich angiogenic inducer 61
glycosylated lysosomal membrane protein
high-mobility group box 1 protein
- MDR2−/− :
knockout of the mdr2 P-glycoprotein gene
matrix metallopeptidase 2
matrix metallopeptidase 9
- RAGE receptor:
receptor for advanced glycation end-products
red blood cells
red cell distribution width
S100 calcium-binding protein A8
S100 calcium-binding protein A9
transmission electron microscopy
tumor growth factor beta
TIMP metallopeptidase inhibitor 1
toll-like receptor 4
tumor necrosis factor alpha
white blood cell
Ballmer PE, Walshe D, McNurlan MA, Watson H, Brunt PW, Garlick PJ. Albumin synthesis rates in cirrhosis: correlation with Child-Turcotte classification. Hepatology. 1993;18:292–7.
Wirawan E, Vanden Berghe T, Lippens S, Agostinis P, Vandenabeele P. Autophagy: for better or for worse. Cell Res. 2012;22:43–61.
Haines DD, Juhasz B, Tosaki A. Management of multicellular senescence and oxidative stress. J Cell Mol Med. 2013;17:936–57.
Schultz ML, Tecedor L, Chang M, Davidson BL. Clarifying lysosomal storage diseases. Trends Neurosci. 2011;34:401–10.
Platt FM, Boland B, van der Spoel AC. Lysosomal storage disorders: the cellular impact of lysosomal dysfunction. J Cell Biol. 2012;199:723–34.
Alroy J, Lyons JA. Lysosomal storage diseases. J Inborn Errors Metabol Screen. 2014;2:1–20.
Parkinson-Lawrence EJ, Shandala T, Prodoehl M, Plew R, Borlace GN, Brooks DA. Lysosomal storage disease: revealing lysosomal function and physiology. Physiology. 2010;25:102–15.
Cox TM, Cachon-Gonzalez MB. The cellular pathology of lysosomal diseases. J Pathol. 2012;226:241–54.
Platt FM, Boland B, van der Spoel AC. The cell biology of disease: lysosomal storage disorders: the cellular impact of lysosomal dysfunction. J Cell Biol. 2012;199:723–34.
Boustany RM. Lysosomal storage diseases—the horizon expands. Nat Rev Neurol. 2013;9:583–98.
Alroy J, Garganta C, Wiederschain G. Secondary biochemical and morphological consequences in lysosomal storage diseases. Biochemistry Biokhimiia. 2014;79:619–36.
Kurz T, Terman A, Gustafsson B, Brunk UT. Lysosomes and oxidative stress in aging and apoptosis. Biochim Biophys Acta. 2008;1780:1291–303.
Kiselyov K, Jennigs Jr JJ, Rbaibi Y, Chu CT. Autophagy, mitochondria and cell death in lysosomal storage diseases. Autophagy. 2007;3:259–62.
Futerman AH, van Meer G. The cell biology of lysosomal storage disorders. Nat Rev Mol Cell Biol. 2004;5:554–65.
Walkley SU. Pathogenic cascades in lysosomal disease—why so complex? J Inherit Metab Dis. 2009;32:181–9.
Pellicoro A, Ramachandran P, Iredale JP, Fallowfield JA. Liver fibrosis and repair: immune regulation of wound healing in a solid organ. Nat Rev Immunol. 2014;14:181–94.
Bataller R, Brenner DA. Liver fibrosis. J Clin Invest. 2005;115:209–18.
Pinzani M, Macias-Barragan J. Update on the pathophysiology of liver fibrosis. Expert Rev Gastroenterol Hepatol. 2010;4:459–72.
Hernandez-Gea V, Friedman SL. Pathogenesis of liver fibrosis. Annu Rev Pathol. 2011;6:425–56.
Friedman SL. Mechanisms of hepatic fibrogenesis. Gastroenterology. 2008;134:1655–69.
Marra F, Tacke F. Roles for chemokines in liver disease. Gastroenterology. 2014;147:577-94.
Pellicoro A, Ramachandran P, Iredale JP. Reversibility of liver fibrosis. Fibrogen Tissue Repair. 2012;5:S26.
Ismail MH, Pinzani M. Reversal of hepatic fibrosis: pathophysiological basis of antifibrotic therapies. Hepat Med. 2011;3:69–80.
Pinzani M, Rosselli M, Zuckermann M. Liver cirrhosis. Best Pract Res Clin Gastroenterol. 2011;25:281–90.
Tsochatzis EA, Bosch J, Burroughs AK. Liver cirrhosis. Lancet. 2014;383:1749–61.
Hayashi H, Sakai T. Animal models for the study of liver fibrosis: new insights from knockout mouse models. Am J Physiol Gastrointest Liver Physiol. 2011;300:G729–38.
Starkel P, Leclercq IA. Animal models for the study of hepatic fibrosis. Best Pract Res Clin Gastroenterol. 2011;25:319–33.
Kong XY, Nesset CK, Damme M, Loberg EM, Lubke T, Maehlen J, Andersson KB, Lorenzo PI, Roos N, Thoresen GH, et al. Loss of lysosomal membrane protein NCU-G1 in mice results in spontaneous liver fibrosis with accumulation of lipofuscin and iron in Kupffer cells. Dis Model Mech. 2014;7:351–62.
Gressner AM, Lotfi S, Gressner G, Haltner E, Kropf J. Synergism between hepatocytes and Kupffer cells in the activation of fat storing cells (perisinusoidal lipocytes). J Hepatol. 1993;19:117–32.
Engelhardt NV, Factor VM, Yasova AK, Poltoranina VS, Baranov VN, Lasareva MN. Common antigens of mouse oval and biliary epithelial cells. Expression on newly formed hepatocytes. Differentiation. 1990;45:29–37.
Grossi CE, Velardi A, Cooper MD. Postnatal liver hemopoiesis in mice: generation of pre-B cells, granulocytes, and erythrocytes in discrete colonies. J Immunol. 1985;135:2303–11.
Schmidt AM, Yan SD, Yan SF, Stern DM. The multiligand receptor RAGE as a progression factor amplifying immune and inflammatory responses. J Clin Invest. 2001;108:949–55.
Sims GP, Rowe DC, Rietdijk ST, Herbst R, Coyle AJ. HMGB1 and RAGE in inflammation and cancer. Annu Rev Immunol. 2010;28:367–88.
Jalan R, Schnurr K, Mookerjee RP, Sen S, Cheshire L, Hodges S, Muravsky V, Williams R, Matthes G, Davies NA. Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality. Hepatology. 2009;50:555–64.
Gue CS, Yap CK, Ng HS. The correlation between cytopenia and esophageal varices in patients with liver cirrhosis. Med J Malaysia. 2004;59:604–8.
Harbour JW, Luo RX, Dei Santi A, Postigo AA, Dean DC. Cdk phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1. Cell. 1999;98:859–69.
Foulkes WD, Flanders TY, Pollock PM, Hayward NK. The CDKN2A (p16) gene and human cancer. Mol Med. 1997;3:5–20.
Puche JE, Saiman Y, Friedman SL. Hepatic stellate cells and liver fibrosis. Comprehen Physiol. 2013;3:1473–92.
Kong XY, Kase ET, Herskedal A, Schjalm C, Damme M, Nesset CK, Thoresen GH, Rustan AC, Eskild W. Lack of the lysosomal membrane protein, GLMP, in mice results in metabolic dysregulation in liver. PLoS One. 2015;10:e0129402.
Popov Y, Patsenker E, Fickert P, Trauner M, Schuppan D. Mdr2 (Abcb4)-/- mice spontaneously develop severe biliary fibrosis via massive dysregulation of pro- and antifibrogenic genes. J Hepatol. 2005;43:1045–54.
Katzenellenbogen M, Pappo O, Barash H, Klopstock N, Mizrahi L, Olam D, Jacob-Hirsch J, Amariglio N, Rechavi G, Mitchell LA, et al. Multiple adaptive mechanisms to chronic liver disease revealed at early stages of liver carcinogenesis in the Mdr2-knockout mice. Cancer Res. 2006;66:4001–10.
Schilsky ML, Quintana N, Volenberg I, Kabishcher V, Sternlieb I. Spontaneous cholangiofibrosis in Long-Evans Cinnamon rats: a rodent model for Wilson’s disease. Lab Anim Sci. 1998;48:156–61.
Brunt EM, Blomenkamp K, Ahmed M, Ali F, Marcus N, Teckman J. Hepatic progenitor cell proliferation and liver injury in alpha-1-antitrypsin deficiency. J Pediatr Gastroenterol Nutr. 2010;51:626–30.
Warskulat U, Borsch E, Reinehr R, Heller-Stilb B, Monnighoff I, Buchczyk D, Donner M, Flogel U, Kappert G, Soboll S, et al. Chronic liver disease is triggered by taurine transporter knockout in the mouse. FASEB J. 2006;20:574–6.
Marhenke S, Buitrago-Molina LE, Endig J, Orlik J, Schweitzer N, Klett S, Longerich T, Geffers R, Sanchez Munoz A, Dorrell C, et al. p21 promotes sustained liver regeneration and hepatocarcinogenesis in chronic cholestatic liver injury. Gut. 2014;63:1501–12.
Afdhal N, McHutchison J, Brown R, Jacobson I, Manns M, Poordad F, Weksler B, Esteban R. Thrombocytopenia associated with chronic liver disease. J Hepatol. 2008;48:1000–7.
Malhi H, Guicciardi ME, Gores GJ. Hepatocyte death: a clear and present danger. Physiol Rev. 2010;90:1165–94.
Verma S, Jensen D, Hart J, Mohanty SR. Predictive value of ALT levels for non-alcoholic steatohepatitis (NASH) and advanced fibrosis in non-alcoholic fatty liver disease (NAFLD). Liver Int. 2013;33:1398–405.
Kim KH, Chen CC, Monzon RI, Lau LF. Matricellular protein CCN1 promotes regression of liver fibrosis through induction of cellular senescence in hepatic myofibroblasts. Mol Cell Biol. 2013;33:2078–90.
Sell S, Dunsford HA. Evidence for the stem cell origin of hepatocellular carcinoma and cholangiocarcinoma. Am J Pathol. 1989;134:1347–63.
Alison MR, Lovell MJ. Liver cancer: the role of stem cells. Cell Prolif. 2005;38:407–21.
Cohen SM, Ellwein LB. Genetic errors, cell proliferation, and carcinogenesis. Cancer Res. 1991;51:6493–505.
Schaub JR, Malato Y, Gormond C, Willenbring H. Evidence against a stem cell origin of new hepatocytes in a common mouse model of chronic liver injury. Cell Rep. 2014;8:933–9.
Roy CN. Anemia of inflammation. Hematology. 2010;2010:276–80.
Ganz T. Hepcidin and iron regulation, 10 years later. Blood. 2011;117:4425–33.
Nelson JE, Wilson L, Brunt EM, Yeh MM, Kleiner DE, Unalp-Arida A, Kowdley KV, Nonalcoholic Steatohepatitis Clinical Research N. Relationship between the pattern of hepatic iron deposition and histological severity in nonalcoholic fatty liver disease. Hepatology. 2011;53:448–57.
Li T, Huang J, Jiang Y, Zeng Y, He F, Zhang MQ, Han Z, Zhang X. Multi-stage analysis of gene expression and transcription regulation in C57/B6 mouse liver development. Genomics. 2009;93:235–42.
Friedman SL. Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury. J Biol Chem. 2000;275:2247–50.
Miura K, Kodama Y, Inokuchi S, Schnabl B, Aoyama T, Ohnishi H, Olefsky JM, Brenner DA, Seki E. Toll-like receptor 9 promotes steatohepatitis by induction of interleukin-1beta in mice. Gastroenterology. 2010;139:323–34. e327.
Su GL. Lipopolysaccharides in liver injury: molecular mechanisms of Kupffer cell activation. Am J Physiol Gastrointest Liver Physiol. 2002;283:G256–65.
Rivera CA, Adegboyega P, van Rooijen N, Tagalicud A, Allman M, Wallace M. Toll-like receptor-4 signaling and Kupffer cells play pivotal roles in the pathogenesis of non-alcoholic steatohepatitis. J Hepatol. 2007;47:571–9.
Grinko I, Geerts A, Wisse E. Experimental biliary fibrosis correlates with increased numbers of fat-storing and Kupffer cells, and portal endotoxemia. J Hepatol. 1995;23:449–58.
Ramachandran A, Prabhu R, Thomas S, Reddy JB, Pulimood A, Balasubramanian KA. Intestinal mucosal alterations in experimental cirrhosis in the rat: role of oxygen free radicals. Hepatology. 2002;35:622–9.
Wiest R, Garcia-Tsao G. Bacterial translocation (BT) in cirrhosis. Hepatology. 2005;41:422–33.
Schwabe RF, Seki E, Brenner DA. Toll-like receptor signaling in the liver. Gastroenterology. 2006;130:1886–900.
Canbay A, Feldstein AE, Higuchi H, Werneburg N, Grambihler A, Bronk SF, Gores GJ. Kupffer cell engulfment of apoptotic bodies stimulates death ligand and cytokine expression. Hepatology. 2003;38:1188–98.
Su GL, Goyert SM, Fan MH, Aminlari A, Gong KQ, Klein RD, Myc A, Alarcon WH, Steinstraesser L, Remick DG, et al. Activation of human and mouse Kupffer cells by lipopolysaccharide is mediated by CD14. Am J Physiol Gastrointest Liver Physiol. 2002;283:G640–5.
Matsuoka M, Tsukamoto H. Stimulation of hepatic lipocyte collagen production by Kupffer cell-derived transforming growth factor beta: implication for a pathogenetic role in alcoholic liver fibrogenesis. Hepatology. 1990;11:599–605.
Santoni-Rugiu E, Jelnes P, Thorgeirsson SS, Bisgaard HC. Progenitor cells in liver regeneration: molecular responses controlling their activation and expansion. APMIS. 2005;113:876–902.
Seki E, De Minicis S, Osterreicher CH, Kluwe J, Osawa Y, Brenner DA, Schwabe RF. TLR4 enhances TGF-beta signaling and hepatic fibrosis. Nat Med. 2007;13:1324–32.
We thank Ingeborg Løstegaard Goverud (Oslo University Hospital), Hilde Letnes, and Hilde C. Bergvin Hyldmo (University of Oslo) for the expert technical assistance.
This work was supported by the Norwegian Research Council [NFR 240844 NCD].
The authors declare that they have no competing interests.
CKN, XYK, MD, CS, and WE conceived and designed the study. CKN, XYK, MD, CS, NR, and EML carried out the experiments and analyzed the data. XYK, CKN, MD, and WE wrote the manuscript. WE and XYK provided the mouse lines. All authors read and approved the final manuscript.
This file provides the sequences of the primer-pairs used for qPCR. (DOC 38 kb)
Extrahepatic tissues show no phenotypic changes. Wild-type (WT) and Glmp gt/gt mice were sacrificed 6 months of age, and the lung, kidney, heart, spleen, and colon were extracted, embedded in paraffin and sectioned. (A) Tissue sections were stained with hematoxylin and eosin or (B) acid fuchsin orange G (blue). Scale bars, 200 μm. (C) WT and Glmp gt/gt mice were perfusion fixated with 4 % formaldehyde and 2.5 % glutaraldehyde. The lung, kidney, heart, spleen, and colon were extracted, sectioned, and analyzed with transmission electron microscopy. Scale bars, 2 μm. (PDF 403 kb)
Glmp gt/gt mice have reduced serum TGF-β levels. Blood serum was collected from wild-type (WT) and Glmp gt/gt mice at 3 weeks, 3 months, and 15 months of age. Serum concentrations of TGF-β were analyzed using enzyme-linked immunosorbent assay (n = 5, *p < 0.05, **p < 0.01, ***p < 0.005 vs. WT). Values are presented as mean ± s.e.m. (PDF 111 kb)
Old Glmp gt/gt mice develop liver tumors. Wild-type (WT) and Glmp gt/gt mice were sacrificed 18 months of age, and the livers were extracted. (A) Representative images show the presence of a hemangioma-like tumor (arrow) and a hepatocellular tumor (arrowheads) in Glmp gt/gt livers. Scale bar, 1 cm. (B) Glmp gt/gt livers stained with hematoxylin and eosin revealed tumors of hepatocellular origin (stars mark circumference of tumor) and (C) hemangioma-like tumors with dilated, blood-filled vessels spindle cell proliferation (arrows). Scale bar, 400 μm. (PDF 112 kb)
Serum functional parameters in old mice. Blood serum was collected from wild-type (WT) and Glmp gt/gt mice at 18 months of age. Serum concentrations of (A) alanine transaminase , (B) aspartate transaminase (AST), (C) bile acids, and (D) albumin were analyzed (n = 6–11, *p < 0.05, **p < 0.01, ***p < 0.005 vs. WT). Values are presented as mean ± s.e.m. (PDF 91 kb)
Total hepatic collagen contents in 18 months old wild-type (WT) and Glmp gt/gt mice were assessed by analyzing liver hydroxyproline content (n = 4, *p < 0.05, **p < 0.01, ***p < 0.005 vs. WT). Values are presented as mean ± s.e.m. (PDF 81 kb)
About this article
Cite this article
Nesset, C.K., Kong, X.Y., Damme, M. et al. Age-dependent development of liver fibrosis in Glmp gt/gt mice. Fibrogenesis Tissue Repair 9, 5 (2016). https://doi.org/10.1186/s13069-016-0042-4
- Liver fibrosis
- Transgenic mouse model
- Liver tumors
- Oval cells