Liver fibrosis is associated with infiltrating immune cells and activation of hepatic stellate cells. We here aimed to investigate the effects of the CC chemokine CCL3, also known as macrophage inflammatory protein-1α, in two different fibrosis models. To this end, we treated mice either with carbon tetrachloride or with a methionine- and choline-deficient diet to induce fibrosis in CCL3 deficient and wild-type mice. The results show that the protein expression of CCL3 is increased in wild-type mice after chronic liver injury. Deletion of CCL3 exhibited reduced liver fibrosis compared to their wild-type counterparts. We could validate these results by treating the two mouse groups with either carbon tetrachloride or by feeding a methionine- and choline-deficient diet. In these models, lack of CCL3 is functionally associated with reduced stellate cell activation and liver immune cell infiltration. In vitro, we show that CCL3 leads to increased proliferation and migration of hepatic stellate cells. In conclusion, our results define the chemokine CCL3 as a mediator of experimental liver fibrosis. Thus, therapeutic modulation of CCL3 might be a promising target for chronic liver diseases.
Citation: Heinrichs D, Berres M-L, Nellen A, Fischer P, Scholten D, Trautwein C, et al. (2013) The Chemokine CCL3 Promotes Experimental Liver Fibrosis in Mice. PLoS ONE 8(6): e66106. https://doi.org/10.1371/journal.pone.0066106
Editor: Bernhard Ryffel, French National Centre for Scientific Research, France
Received: February 21, 2013; Accepted: May 2, 2013; Published: June 17, 2013
Copyright: © 2013 Heinrichs et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by grants from the Deutsche Forschungsgemeinschaft (WA 2557/2-1 and SFB/TRR 57) and the Else Kröner-Fresenius Stiftung to H.E.W. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Liver fibrosis frequently progresses to end-stage liver disease including liver cirrhosis and hepatocellular carcinoma, which are mainly caused by viruses, metabolic diseases and alcohol , . It is a result of a chronic wound healing process leading to an inflammatory and fibrotic response . Hepatic stellate cells (HSCs), the main fibrogenic resident cells in the liver, play an essential role during this fibrotic response. Following a fibrogenic stimulus, hepatic stellate cells transdifferentiate from quiescent vitamin A-storing cells into activated cell types which produce a large amount of ECM proteins. The inflammatory response during chronic hepatocyte injury triggers the accumulation of immune cells in the liver consisting of e.g. T cells, macrophages, and dendritic cells . The recruitment of these cells is orchestrated by the pattern of cytokines and chemokines which are secreted by activated liver resident cells , . Among these cells, hepatic stellate cells secrete a wide range of chemokines (CCL2, CCL3, CCL5 CCL11, CXCL8, CXCL9, and CXCL10), thereby influencing the quantity and also the quality of the inflammatory response , . Beside regulation of liver inflammation, the chemokines CCL2, CCL5 and CXCL9 has also been identified to directly influence the biology of hepatic stellate cells –.
In the present study, we focus on the chemokine CCL3, which is also known as macrophage inflammatory protein-1α. Murine CCL3 is located on chromosome 11 and is encoded by a single-copy gene . It consists of three exons and two introns, which codes for a pre-protein of 92 amino acids . CCL3 is a 7.8 kDa CC chemokine which is strongly expressed by numerous cell types including T cells, macrophages, neutrophils, endothelial and also stellate cells upon injury –.
This chemokine recruits several cell types, like T cells, neutrophils and eosinophils – to site of inflammation by interacting with its receptors CCR1 and CCR5 . Interestingly, hepatic stellate cells also express CCR5, identifying these cells as a source as well as a target of CCL3 within the liver. Moreover, CCR1 and CCR5 deficient mice showed a lower degree of liver fibrosis after chronic carbon tetrachloride (CCl4) treatment or bile duct ligation (BDL) . Studies of fibrogenesis in CCR1 and CCR5 chimeric mice revealed a divergent function of these chemokine receptors in the liver. CCR1 mediates its pro-fibrotic effects predominantly through hematopoietic cells, whereas CCR5 mediates liver fibrosis mainly through resident liver cells . CCL5 seems to be a crucial mediator of this chemokine pathway as CCL5−/− mice also show reduced liver fibrosis induced by carbon tetrachloride (CCl4) or methionine- and choline-deficient (MCD) diet. Importantly, administration of mice with Met-CCL5, a CCR1/CCR5 antagonist, attenuated liver fibrosis and accelerated the regression of fibrosis during follow-up . A crucial role for this chemokine has also been established in Concanavalin A (ConA) mediated liver injury , a model of T cell mediated hepatitis . In this model, CCL3−/− mice were significantly rescued from liver failure due to reduced recruitment of CCR1-expressing CD4+ T cells . The effects of CCL3 make this CCR1/CCR5 ligand attractive for further evaluation in experimental liver fibrosis.
In line with these previous data, we here show that CCL3 is an important mediator of experimental liver fibrosis by its dual effects on hepatic stellate cells and intrahepatic immune environment. Thus, CCL3 represent a potential target for antifibrotic therapies.
Materials and Methods
Murine in vivo Experiments
Male C57BL/6 wild-type (WT, CCL3+/+, 8–10 weeks) mice were routinely purchased from the Jackson Laboratory and acclimated for at least 1 week before any experiments were conducted. CCL3 deficient (CCL3−/−) mice, also purchased from the Jackson Laboratory, were maintained on C57BL/6 background and bred in our animal housing facility. Only male littermates (8–10 weeks) were used in experiments. All in vivo experiments were performed following approval by the state animal protection board at the Bezirksregierung Cologne, Germany (Permit Number: 8.84–02.04.20.11). CCL3−/− and wild-type mice were subjected to two different fibrosis models. In the first experiment, CCL3−/− and WT mice received intraperitoneal injections of carbon tetrachloride (CCl4; 0.6 ml/kg bodyweight) for six weeks. Three days after the last injection, the mice were sacrificed . In the second experiment, the mice were fed a methionine- and choline-deficient diet (MCD; MP Biomedicals Europe) for eight weeks. In both models the size were n = 8 per group.
Quantification of Liver Fibrosis
In all animals, liver fibrosis was determined by quantitative analysis of the Sirius red staining from liver sections. Liver sections were quantified by the Sirius red-positive area using the NIH ImageJ software (http://rsbweb.nih.gov/). Moreover, the collagen-specific amino acid hydroxyproline were determined in the liver samples. The hydroxyproline contents were measured colorimetric as described previously .
Quantification of Hepatocellular Damage
The terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labelling (TUNEL) assay (Roche) was performed to detect and quantify hepatocellular damage within the liver. The percentage of TUNEL+ cells was determined in 3 independent magnification fields per mouse.
Expression Analysis of Fibrosis and Inflammation Related Genes
Isolation of total RNA from snap-frozen liver samples were performed and total RNA was transcribed into cDNA with the RevertAid™ Premium First Strand cDNA Synthesis Kit (Fermentas). Following quantitative RT-PCR for the genes, TGF-β1, Col1a1, TIMP1, MMP9, α-SMA, SREBP1, Fas, TNF-α, IL-1β, MCP-1 and IL-2 was executed with Assay-on-Demand (Applied Biosystems).
For protein isolation, liver samples were homogenized in RIPA buffer with protease inhibitor (Mini Complete Protease Inhibitor Cocktail Tablets, Roche Applied Science) and centrifuged; supernatants were collected and stored at −80°C. After thawing, the hepatic CCL3 contents were measured in supernatants using a murine ELISA (R&D Systems) in duplicate, following the manufacturer’s instructions. The OD of the samples was determined at a wavelength of 450 nm. CCL3 concentrations are expressed in pg per mg of total liver protein.
Hepatic Immune Cell Isolation and Flow Cytometry Analysis
Flow cytometry analysis of hepatic immune cells was performed by isolating single cell suspension from freshly harvested liver . The cells were isolated by mechanical and enzymatic digestion. Viable white blood cells were separated by centrifugation for 20 minutes at 800 g. After the density gradient centrifugation, the isolated peripheral blood mononuclear cells (PBMCs) were washed with Hank’s buffer supplemented with 1% BSA and 2 mM EDTA. Cells were stained with antibodies for CD45, CD3, CD4, CD8 and NK1.1 (eBioscience) and then measured with BD FACSCanto II (BD Bioscience).
Immunohistochemical Staining of Murine Liver Tissue
Immunohistochemical staining of immune and stellate cells was performed with paraffin-embedded sections of liver tissue. Leukocytes were stained with a monoclonal rat anti-mouse CD45 antibody (BD). Staining for T cells was performed with a monoclonal rabbit anti-mouse CD3 antibody (LabVision). Macrophages were analyzed by using a monoclonal rat anti-mouse F4/80 antibody (BMA Dianova). Analyzing the activation of stellate cells a monoclonal rabbit anti-mouse α-SMA antibody (Biomol/Epitomics) was used.
Cell Proliferation Assay
The proliferation of hepatic stellate cell line GRX was determined with Cell Proliferation ELISA (Roche Applied Science). Cell Proliferation ELISA based on the measurement of BrdU incorporation during the DNA synthesis. The cells were starved in DMEM medium (PAA Laboratories) without FCS for 16 hours. Then, the cells were stimulated with 20 ng of recombinant CCL3 for 24 and 32 hours. After the stimulation, cells were labelled with BrdU for additional 2 hours. The cells were washed and fixed, and the amount of BrdU, which has been incorporated into the DNA, was detected by adding an anti-BrdU peroxidase antibody and TMB substrate solution. The substrate reaction was measured at a wavelength of 370 nm.
Assessment of Cell Proliferation and Migration in a Scratch Assay
Additionally, hepatic stellate cell migration and proliferation were performed in a scratch assay. After the cells were confluent in 6-well plates, a straight scratch with a pipette tip (blue, Gilson) was created on the cell monolayer. The cells were stimulated for 24 and 32 hours with recombinant CCL3. To quantify cell migration and proliferation the width of the scratch was recorded and measured digitally (x100 magnification) before and after stimulation in order to calculate the percentage of regrowed area.
Data are depicted as mean ± SEM. Statistical significance was assessed by two-way analysis of variance followed by a Student’s t test, with Welch’s correction in case of unequal variances. P values under 0.05 were considered significant in all cases. Statistical analyses were performed using GraphPad Prism 5.
CCL3−/− Mice Displayed Ameliorated Liver Fibrosis
First, we evaluated intrahepatic CCL3 levels before and after feeding a methionine- and choline-deficient (MCD) diet for eight weeks. We found that CCL3 protein expression is significantly increased after MCD diet when compared to untreated controls (Fig. 1A, P<0.05).
CCL3 expression is increased in MCD-fed wild-type mice compared to untreated control (A). Representative Sirius red staining of CCL3−/− and wild-type (CCL3+/+) mice after MCD diet (x100 magnification). Quantitative analysis of the Sirius red-positive area showed a significantly decrease in CCL3−/− mice compared to wild-type mice (B). Hydroxyproline concentration in the liver (C) and serum level of ALT (D) were also significantly decreased in CCL3−/− mice. Data are expressed as means ± SEM of eight mice per group. *P<0.05, ***P<0.001.
CCL3 is increased after MCD feeding; hence we tested if deletion of CCL3 has an impact on liver fibrosis. CCL3−/− and wild-type (CCL3+/+) mice were fed a MCD diet for eight weeks. MCD-fed CCL3−/− animals showed significantly reduced liver fibrosis compared to CCL3+/+ mice. This difference was evident after quantification of Sirius red stained liver tissues (Fig. 1B, P<0.001) and biochemical measurement of hepatic hydroxyproline contents (Fig. 1C, P<0.05). Serum levels of alanine aminotransferase (ALT) were also significantly lower in CCL3−/− animals (Figure 1D; P<0.05) after feeding with the MCD diet.
Liver Injury in CCL3−/− Mice is Associated with Altered Fibrosis and Lipogenesis Related Factors
In a next step, we investigated the expression of fibrosis-related genes in the liver of MCD-fed CCL3−/− and CCL3+/+ mice, which are involved in the deposition and remodelling of extracellular matrix. As depicted in figure 2A, reduced liver fibrosis in CCL3−/− mice was associated with altered expression of Col1a1, TIMP1, and MMP9 (Fig. 2A, P<0.05). In contrast, mRNA expression of TGF-β1 (Fig. 2A) and MMP2 (data not shown) did not vary in CCL3−/− mice. Since these genes are also evident in the biology of hepatic stellate cells, we next assessed liver HSC activation after chronic liver injury. HSC activation was significantly reduced in CCL3−/− mice after MCD diet, as determined by immunohistochemical staining and quantitative real-time PCR analysis of α-SMA (Fig. 2B, P<0.05).
MCD-fed CCL3−/− mice show a significantly altered expression of the fibrosis-related genes Col1a1, TIMP1 and MMP9 compared to wild-type mice. However, mRNA expression of TGF-β1 does not vary in CCL3−/− mice (A). α-SMA expression is significantly decreased in CCL3−/− mice after MCD diet. Representative α-SMA staining is shown in the left panel (x100 magnification, B). Data are expressed as means ± SEM of eight mice per group. *P<0.05.
Moreover, CCL3−/− mice showed significantly reduced hepatic and serum triglyceride levels when compared to CCL3+/+ mice (Figure S1A and B, P<0.05), suggesting that CCL3 might also operate in metabolic disease. These results were further confirmed by significantly reduced intraheptic mRNA expression of the lipogenic factors SREBP1 and Fas (Figure S1C and D, P<0.05).
CCL3−/− Mice had Reduced Liver Fibrosis after CCl4 Challenge
Next, we asked if the effect on dietary-induced liver damage also holds true in the CCl4 model of liver fibrosis. Intrahepatic CCL3 protein expression in untreated wild-type mice was compared to CCL3 protein level in wild-type mice after acute and chronic CCl4 treatment. As depicted in figure 3A, acute CCl4-mediated liver injury induced significantly higher CCL3 expression (P<0.05), while after chronic CCl4 treatment only a trend towards higher CCL3 expression was evident.
Acute liver injury after CCl4 challenge is associated with augmented hepatic expression of CCL3, while CCL3 after chronic CCl4 treatment has a tendency toward higher expression (A). Sirius red staining after the CCl4 treatment (x100 magnification) shows reduced liver fibrosis in CCL3 deficient mice (B). Hydroxyproline contents in the liver (C) and serum level of ALT (D) were significantly decreased in CCL3−/− mice. Data are expressed as means ± SEM of eight mice per group. *P<0.05, **P<0.01, ***P<0.001.
Along with the data in the MCD model histological analysis of Sirius red staining revealed reduced liver fibrosis in CCL3 deficient mice after chronic CCl4 treatment (Fig. 3B, P<0.001). These results were further strengthened by markedly reduced concentrations of the collagen-specific amino acid hydroxyproline (Fig. 3C, P<0.01). Moreover, ALT values (Fig. 3D, P<0.05) and TUNEL+ cells within the liver (Figure S2A *P<0.05) were also reduced in CCL3−/− mice compared to wild-type control, suggesting a directly involvement of CCL3 in inflammatory hepatocyte damage.
Liver Damage after Chronic CCl4 Treatment Led to Altered Expression of Fibrosis-Related Genes in CCL3−/− Mice
In liver fibrosis, one of the key events is HSC activation. To investigate this process, fibrosis-related genes, which are involved in HSC biology, were analyzed. mRNA expression of the fibrogenic genes TGF-β1, Col1a1, TIMP1 and MMP9 were significantly altered in CCL3−/− mice compared to their wild-type counterparts after chronic CCl4 treatment (Fig. 4A, P<0.05, P<0.001 and P<0.01, respectively), while MMP2 levels were not significantly different between the two strains (data not shown). Alongside with data obtained in dietary-induced liver damage model, the level of α-SMA was also significantly reduced in CCL3−/− mice compared to controls (Fig. 4B). This difference was true after genetic (P<0.05) and immunohistochemical analyses of α-SMA. These findings suggest a model independent profibrotic mechanism of CCL3 during liver fibrosis.
CCl4 treatment of CCL3−/− mice lead to significantly altered expression of the fibrosis-related genes Col1a1, TGF-β1, TIMP1 and MMP9 in CCL3−/− mice (A). α-SMA expression is significantly decreased in CCL3−/− mice (x100 magnification, B). Data are expressed as means ± SEM of eight mice per group. *P<0.05, **P<0.01, ***P<0.001.
Inflammation-related Genes and the Number of T Cells are Reduced in CCL3−/− Mice Treated with CCl4
Immune cells contribute to liver fibrogenesis , ; we first investigated inflammation-related genes by quantitative RT-PCR analysis. Compared to WT mice, mRNA expression of TNF-α, IL-1β, IL-2 and also MCP-1 (monocyte chemoattractant protein-1, CCL2) was markedly reduced in CCL3 deficient mice (Fig. 5A, P<0.05). Consequently, we investigated immune cell infiltrating by FACS analysis and immunohistochemistry. FACS analysis revealed markedly reduced hepatic infiltration of T cells and, specifically of CD8+ T cells in CCL3−/− mice (Fig. 5B, P = 0.07 and P = 0.03, respectively), while the influx of NK and NKT cells were not strongly affected (data not shown). These results were further confirmed by quantification of absolute immune cell numbers within the liver (Figure S2B, P = 0.053 and P<0.05, respectively). By immunohistochemical quantification of representative liver sections, we found reduced numbers of CD45+ and CD3+ cells (Fig. 6A and B, P<0.001 and P<0.05, respectively) and also F4/80+ macrophages (Figure S3, P<0.05) within CCL3 deficient livers treated with CCl4.
CCL3−/− mice treated with CCl4 show altered expression of the inflammation-related genes TNF-α, IL-1β, IL-2 and MCP-1 compared to wild-type mice (A). CD8+ T cell infiltration is significantly decreased in CCL3−/− mice (B). Data are expressed as means ± SEM of eight mice per group. *P<0.05.
CCL3 Accelerated the Proliferation of HSC in vitro
Finally, we investigated the direct effects of the chemokine on the immortalized hepatic stellate cell line GRX in vitro. As depicted in figure 7A, CCL3 significantly increased stellate cell proliferation (P<0.001), as determined by BrdU incorporation. Furthermore, CCL3 accelerated scratch closure triggered by enhanced proliferation and migration of stellate cells in a functional scratch assay (Fig. 7B and Figure S4). This effect was first observed 32 hours after incubation (P<0.001).
Stimulation of hepatic stellate cell line (GRX) with recombinant CCL3 led to significantly increased proliferation compared to untreated cells (A). Stimulation of GRX cells with recombinant CCL3 showed significantly increased wound healing after 32 hours, while there is no difference after 24 hours between the groups (B). Data are expressed as means ± SEM of three independent experiments. ***P<0.001.
In our study, we demonstrate a pro-fibrotic effect of the CC chemokine CCL3 in two independent fibrosis models. Initially, we could show that CCL3 protein expression is significantly up-regulated in wild-type mice after methionine- and choline-deficient diet and acute CCl4 treatment, however, CCL3 protein expression was only moderate altered six weeks after CCl4 treatment. These observations are in accordance with data on pulmonary fibrosis  showing an increased intrapulmonary CCL3 level during the early inflammatory phase in response to thoracic irradiation and supported our assumption that liver resident and inflammatory cells-secreted CCL3 might facilitate immune cell recruitment into the liver, which in turn contributes to the degree of tissue injury .
This chemokine belongs to the intercrine beta (chemokine CC) family and binds to the receptors CCR1 and CCR5 , . Mice lacking any of these receptors were less prone to hepatic fibrogenesis after chronic toxic injury or bile duct ligation . These findings are in line with clinical studies showing an association between the CCR5Δ32 polymorphism and the degree of the HCV-related hepatitis . Furthermore, analysis of fibrogenesis in CCR1 and CCR5 chimeric mice revealed a divergent function of these chemokine receptors in the liver. Interestingly, CCR1 mediates its pro-fibrogenic effects predominantly through hematopoietic cells, whereas CCR5 mediates liver fibrosis mainly through resident liver cells, especially through hepatic stellate cells . Their shared other ligand CCL5 is known to be involved in this process, as CCL5−/− mice also showed lower degree of experimental liver fibrosis associated with reduced stellate cell activation and immune cell infiltration . Accordingly, systemic administration of Met-CCL5 or (44)AANA(47)-CCL5, a mutated CCL5 protein, led to a strong attenuation of experimental liver fibrosis in vivo , . These findings, together with the knowledge that CCL3 is also a prominent ligand of the receptors CCR1 and CCR5, has brought us to further investigate the functional role of CCL3 during experimental liver damage.
Here, we could show that mice lacking CCL3 showed significantly reduced MCD- and CCl4- induced liver fibrosis compared to CCL3+/+ mice, as determined by quantification of Sirius red staining and biochemical measurement of hepatic hydroxyproline contents. These data were obtained in both fibrosis models in vivo, indicating that the functional mechanism of CCL3 is independent of the experimental model used. Notably, CCL3 deficient mice also showed reduced ALT levels and TUNEL+ cells, assuming a direct involvement of CCL3 in inflammatory hepatocyte damage. The genetic deletion of CCL3 indeed led to a reduced hepatic recruitment of T cells and macrophages after liver injury, confirming the hypothesis that reduced T cell and macrophage infiltrate might lead to less collateral damage in the liver, which in turn altered ALT levels . These results are in line with earlier findings of the importance of CCL3 in models of pulmonary fibrosis  and acute liver injury .
In these mice, we also found less stellate cell activity, as determined by α-SMA mRNA and protein expression, an important marker for activated HSCs. These results suggest an interaction between immune and stellate cells which has been recently identified as an important event in liver fibrosis .
To further assess the functional aspect of CCL3 on hepatic stellate cells , we next stimulated these cells with recombinant CCL3 in vitro. Interestingly, CCL3 displayed strong proliferative effect on stellate cells, as determined by BrdU incorporation. Scratch assay analysis also showed significantly increased migration and proliferation of CCL3 treated cells compared to control, confirming these cells as resident target cell type of CCL3 . However, with regard of fibrosis, additional studies will be needed to identify the temporal requirement of CCL3 for these actions.
Taken together, our findings present evidence that the CC chemokine CCL3 is a crucial mediator of experimental liver fibrosis. These preclinical results identify CCL3 as a potential molecular target for therapeutic strategies for chronic toxic and metabolic liver diseases.
CCL3 is involved in metabolic disease. CCL3−/− mice exhibits significantly lower hepatic and serum level of triglycerides compared to CCL3+/+ mice after MCD diet (A, B). Altered triglyceride values were associated with reduced mRNA expression of SREBP1 and Fas (C, D). Data are expressed as means ± SEM of eight mice per group. *P<0.05.
Reduced liver injury and inflammation in CCL3−/− mice. TUNEL+ cells (TUNEL staining, x100 magnification) within the liver were significantly reduced in CCL3−/− mice compared to CCL3+/+ mice after six weeks of CCl4 treatment (A). Absolute CD45+, CD3+ and CD8+ cell numbers are markedly decreased in CCL3−/− mice (B). *P<0.05.
CCL3 deficiency results in reduced influx of macrophages. F4/80+ cells (F4/80 staining, x100 magnification) within the liver were significantly decreased in CCL3−/− mice compared to CCL3+/+ mice after six weeks of CCl4 treatment. *P<0.05.
CCL3 accelerates proliferation and migration of stellate cells. Representative pictures of scratch assay (x200 magnification). The pictures show the scratches after 0, 24 and 32 hours after the stimulation with 20 ng recombinant CCL3.
Conceived and designed the experiments: DH DS CT HEW HS. Performed the experiments: DH MLB AN PF HS. Analyzed the data: DH HS. Wrote the paper: DH HS.
- 1. Bataller R, Brenner DA (2005) Liver fibrosis. J Clin Invest 115: 209–218.
- 2. Friedman SL (2008) Mechanisms of hepatic fibrogenesis. Gastroenterology 134: 1655–1669.
- 3. Sahin H, Wasmuth HE (2012) Chemokines in tissue fibrosis. Biochim Biophys Acta.
- 4. Holt AP, Salmon M, Buckley CD, Adams DH (2008) Immune interactions in hepatic fibrosis. Clin Liver Dis 12: 861–882, x.
- 5. Marra F, Aleffi S, Galastri S, Provenzano A (2009) Mononuclear cells in liver fibrosis. Semin Immunopathol 31: 345–358.
- 6. Karlmark KR, Wasmuth HE, Trautwein C, Tacke F (2008) Chemokine-directed immune cell infiltration in acute and chronic liver disease. Expert Rev Gastroenterol Hepatol 2: 233–242.
- 7. Holt AP, Haughton EL, Lalor PF, Filer A, Buckley CD, et al. (2009) Liver myofibroblasts regulate infiltration and positioning of lymphocytes in human liver. Gastroenterology 136: 705–714.
- 8. Wasmuth HE, Lammert F, Zaldivar MM, Weiskirchen R, Hellerbrand C, et al.. (2009) Antifibrotic effects of CXCL9 and its receptor CXCR3 in livers of mice and humans. Gastroenterology 137: 309–319, 319 e301–303.
- 9. Marra F, Valente AJ, Pinzani M, Abboud HE (1993) Cultured human liver fat-storing cells produce monocyte chemotactic protein-1. Regulation by proinflammatory cytokines. J Clin Invest 92: 1674–1680.
- 10. Berres ML, Koenen RR, Rueland A, Zaldivar MM, Heinrichs D, et al. (2010) Antagonism of the chemokine Ccl5 ameliorates experimental liver fibrosis in mice. J Clin Invest 120: 4129–4140.
- 11. Colobran R, Pedrosa E, Carretero-Iglesia L, Juan M (2010) Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease. Clin Exp Immunol 162: 41–52.
- 12. Menten P, Wuyts A, Van Damme J (2002) Macrophage inflammatory protein-1. Cytokine Growth Factor Rev 13: 455–481.
- 13. Seki E, De Minicis S, Gwak GY, Kluwe J, Inokuchi S, et al. (2009) CCR1 and CCR5 promote hepatic fibrosis in mice. J Clin Invest 119: 1858–1870.
- 14. Berkman N, John M, Roesems G, Jose PJ, Barnes PJ, et al. (1995) Inhibition of macrophage inflammatory protein-1 alpha expression by IL-10. Differential sensitivities in human blood monocytes and alveolar macrophages. J Immunol 155: 4412–4418.
- 15. Takahashi H, Tashiro T, Miyazaki M, Kobayashi M, Pollard RB, et al. (2002) An essential role of macrophage inflammatory protein 1alpha/CCL3 on the expression of host's innate immunities against infectious complications. J Leukoc Biol 72: 1190–1197.
- 16. Bonecchi R, Polentarutti N, Luini W, Borsatti A, Bernasconi S, et al. (1999) Up-regulation of CCR1 and CCR3 and induction of chemotaxis to CC chemokines by IFN-gamma in human neutrophils. J Immunol 162: 474–479.
- 17. Rot A, Krieger M, Brunner T, Bischoff SC, Schall TJ, et al. (1992) RANTES and macrophage inflammatory protein 1 alpha induce the migration and activation of normal human eosinophil granulocytes. J Exp Med 176: 1489–1495.
- 18. Roth SJ, Carr MW, Springer TA (1995) C-C chemokines, but not the C-X-C chemokines interleukin-8 and interferon-gamma inducible protein-10, stimulate transendothelial chemotaxis of T lymphocytes. Eur J Immunol 25: 3482–3488.
- 19. Ajuebor MN, Hogaboam CM, Le T, Proudfoot AE, Swain MG (2004) CCL3/MIP-1alpha is pro-inflammatory in murine T cell-mediated hepatitis by recruiting CCR1-expressing CD4(+) T cells to the liver. Eur J Immunol 34: 2907–2918.
- 20. Ajuebor MN, Hogaboam CM, Le T, Proudfoot AE, Swain MG (2004) CCL3/MIP-1alpha is pro-inflammatory in murine T cell-mediated hepatitis by recruiting CCR1-expressing CD4(+) T cells to the liver. Eur J Immunol 34: 2907–2918.
- 21. Tiegs G, Hentschel J, Wendel A (1992) A T cell-dependent experimental liver injury in mice inducible by concanavalin A. J Clin Invest. 90: 196–203.
- 22. Sahin H, Borkham-Kamphorst E, Kuppe C, Zaldivar MM, Grouls C, et al. (2012) Chemokine Cxcl9 attenuates liver fibrosis-associated angiogenesis in mice. Hepatology 55: 1610–1619.
- 23. Stock MK, Hammerich L, do ON, Berres ML, Alsamman M, et al. (2013) Met-CCL5 modifies monocyte subpopulations during liver fibrosis regression. Int J Clin Exp Pathol 6: 678–685.
- 24. Park O, Jeong WI, Wang L, Wang H, Lian ZX, et al. (2009) Diverse roles of invariant natural killer T cells in liver injury and fibrosis induced by carbon tetrachloride. Hepatology 49: 1683–1694.
- 25. Ishikawa S, Ikejima K, Yamagata H, Aoyama T, Kon K, et al. (2011) CD1d-restricted natural killer T cells contribute to hepatic inflammation and fibrogenesis in mice. J Hepatol 54: 1195–1204.
- 26. Yang X, Walton W, Cook DN, Hua X, Tilley S, et al. (2011) The chemokine, CCL3, and its receptor, CCR1, mediate thoracic radiation-induced pulmonary fibrosis. Am J Respir Cell Mol Biol 45: 127–135.
- 27. Ajuebor MN, Kunkel SL, Hogaboam CM (2004) The role of CCL3/macrophage inflammatory protein-1alpha in experimental colitis. Eur J Pharmacol 497: 343–349.
- 28. Goulding C, McManus R, Murphy A, MacDonald G, Barrett S, et al. (2005) The CCR5-delta32 mutation: impact on disease outcome in individuals with hepatitis C infection from a single source. Gut 54: 1157–1161.
- 29. Nellen A, Heinrichs D, Berres ML, Sahin H, Schmitz P, et al. (2012) Interference with oligomerization and glycosaminoglycan binding of the chemokine CCL5 improves experimental liver injury. PLoS One 7: e36614.
- 30. Vicente CP, Fortuna VA, Margis R, Trugo L, Borojevic R (1998) Retinol uptake and metabolism, and cellular retinol binding protein expression in an in vitro model of hepatic stellate cells. Mol Cell Biochem 187: 11–21.