Partial Hepatectomy–Induced Regeneration Accelerates Reversion of Liver Fibrosis Involving Participation of Hepatic Stellate Cells

Hepatic fibrosis underlies most types of chronic liver diseases and is characterized by excessive deposition of extracellular matrix (ECM), altered liver architecture, and impaired hepatocyte proliferation; however, the fibrotic liver can still regenerate after partial hepatectomy (PH). Therefore, the present study was aimed at addressing whether a PH-induced regeneration normalizes ECM turnover and the possible involvement of hepatic stellate cells (HSC) during resolution of a pre-established fibrosis. Male Wistar rats were rendered fibrotic by intraperitoneal administration of swine serum for 9 weeks and subjected afterwards to 70% PH or sham-operation. Histological and morphometric analyses were performed, and parameters indicative of cell proliferation, collagen synthesis and degradation, and activation of HSC were determined. Liver collagen content was reduced to 75% after PH in cirrhotic rats when compared with sham-operated cirrhotic rats. The regenerating fibrotic liver oxidized actively free proline and had diminished transcripts for α-1 (I) collagen mRNA, resulting in decreased collagen synthesis. PH also increased collagenase activity, accounted for by higher amounts of pro-MMP-9, MMP-2, and MMP-13, which largely coincided with a lower expression of TIMP-1 and TIMP-2. Therefore, an early decreased collagen synthesis, mild ECM degradation, and active liver regeneration were followed by higher collagenolysis and limited deposition of ECM, probably associated with increased mitochondrial activity. Activated HSC readily increased during liver fibrosis and remained activated after liver regeneration, even during fibrosis resolution. In conclusion, stimulation of liver regeneration through PH restores the balance in ECM synthesis/degradation, leading to ECM remodeling and to an almost complete resolution of liver fibrosis. As a response to the regenerative stimulus, activated HSC seem to play a controlling role on ECM remodeling during experimental cirrhosis in rats. Therefore, pharmacological approaches for the resolution of liver fibrosis by blocking HSC activation should also evaluate possible effects on liver cell proliferation.

[1]  M. Hashimoto,et al.  Functional restoration of cirrhotic liver after partial hepatectomy in the rat. , 2005, Hepato-gastroenterology.

[2]  V. Arroyo,et al.  Management of cirrhosis and ascites. , 2004, The New England journal of medicine.

[3]  P. Sheard,et al.  Role of hepatic stellate cell/hepatocyte interaction and activation of hepatic stellate cells in the early phase of liver regeneration in the rat. , 2004, Journal of hepatology.

[4]  R. Khokha,et al.  Thinking outside the cell: proteases regulate hepatocyte division. , 2005, Trends in cell biology.

[5]  A. Mori,et al.  Simultaneous transfer of vascular endothelial growth factor and hepatocyte growth factor genes effectively promotes liver regeneration after hepatectomy in cirrhotic rats. , 2004, Hepato-gastroenterology.

[6]  R. Hernández-Muñoz,et al.  Adenosine partially prevents cirrhosis induced by carbon tetrachloride in rats , 1990, Hepatology.

[7]  P. Norton,et al.  Animal models of liver fibrosis. , 1996, Scandinavian journal of gastroenterology.

[8]  A. Strongin,et al.  Interaction of 92-kDa type IV collagenase with the tissue inhibitor of metalloproteinases prevents dimerization, complex formation with interstitial collagenase, and activation of the proenzyme with stromelysin. , 1992, The Journal of biological chemistry.

[9]  R. Hernández-Muñoz,et al.  Changes in mitochondrial adenine nucleotides and in permeability transition in two models of rat liver regeneration , 2003, Hepatology.

[10]  A. Luder,et al.  The Beneficial Effect of Aspirin and Enoxaparin on Fibrosis Progression and Regenerative Activity in a Rat Model of Cirrhosis , 2007, Digestive Diseases and Sciences.

[11]  A. Nagler,et al.  Halofuginone to prevent and treat thioacetamide‐induced liver fibrosis in rats , 2001, Hepatology.

[12]  Stefano Colagrande,et al.  Fibrosis in chronic liver diseases: diagnosis and management. , 2005, Journal of hepatology.

[13]  S. Friedman,et al.  Hepatic fibrosis. Pathogenesis and principles of therapy , 2001 .

[14]  S. Dooley,et al.  Molecular Mechanisms of Alcohol-Induced Hepatic Fibrosis , 2006, Digestive Diseases.

[15]  R. Hernández-Muñoz,et al.  Inhibitory Effect of Vitamin E Administration on the Progression of Liver Regeneration Induced by Partial Hepatectomy in Rats , 2003, Laboratory Investigation.

[16]  Antonio Martinez‐Hern Andez,et al.  The extracellular matrix in hepatic regeneration , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[17]  C. Rudin,et al.  Apoptosis and disease: regulation and clinical relevance of programmed cell death. , 1997, Annual review of medicine.

[18]  R. Perez-Tamayo,et al.  Collagenase of hepatocytes and sinusoidal liver cells in the reversibility of experimental cirrhosis of the liver , 1990, Virchows Archiv. B, Cell pathology including molecular pathology.

[19]  D. Schuppan,et al.  Matrix as a modulator of hepatic fibrogenesis. , 2001, Seminars in liver disease.

[20]  J. Iredale,et al.  Galectin-3 regulates myofibroblast activation and hepatic fibrosis. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[21]  V. Paradis,et al.  Liver extracellular matrix in health and disease , 2003, The Journal of pathology.

[22]  C. Guguen-Guillouzo,et al.  TNFα‐mediated extracellular matrix remodeling is required for multiple division cycles in rat hepatocytes , 2005, Hepatology.

[23]  M. Coëffier,et al.  Changes in growth factor and cytokine mRNA levels after hepatectomy in rat with CCl4-induced cirrhosis. , 1999, American Journal of Physiology - Gastrointestinal and Liver Physiology.

[24]  A. Ooshima,et al.  Combination gene therapy of HGF and truncated type II TGF-beta receptor for rat liver cirrhosis after partial hepatectomy. , 2006, Surgery.

[25]  G. Ramadori,et al.  Expression of matrix metalloproteinases and their inhibitors during hepatic tissue repair in the rat , 2000, Histochemistry and Cell Biology.

[26]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[27]  D. Rockey Hepatic fibrosis, stellate cells, and portal hypertension. , 2006, Clinics in liver disease.

[28]  M. Arthur,et al.  Reversibility of liver fibrosis and cirrhosis following treatment for hepatitis C. , 2002, Gastroenterology.

[29]  M. Rojkind,et al.  An improved method for determining specific radioactivities of proline-14C and hydroxyproline-14C in collagen and in noncollagenous proteins. , 1974, Analytical biochemistry.

[30]  R. Hernández-Muñoz,et al.  Possible role of cell redox state on collagen metabolism in carbon tetrachloride-induced cirrhosis as evidenced by adenosine administration to rats. , 1994, Biochimica et biophysica acta.

[31]  Li-juan Zhang,et al.  Expression of matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-1 in hepatic stellate cells during rat hepatic fibrosis and its intervention by IL-10. , 2005, World journal of gastroenterology.

[32]  T. Nouchi,et al.  Phenotypic modulation in lipocytes in experimental liver fibrosis , 1991, The Journal of pathology.

[33]  A. Ayhan,et al.  Lipid peroxidation and extracellular matrix in normal and cirrhotic rat livers following 70% hepatectomy. , 2003, Hepato-gastroenterology.

[34]  B. Ahrén,et al.  Liver cirrhosis in rats: regeneration and assessment of the role of phenobarbital. , 1991, The Journal of surgical research.

[35]  Masao Tanaka,et al.  Inhibited activities in CCAAT/enhancer-binding protein, activating protein-1 and cyclins after hepatectomy in rats with thioacetamide-induced liver cirrhosis. , 2002, Biochemical and biophysical research communications.

[36]  R. Khokha,et al.  Metalloproteinase inhibitor TIMP‐1 affects hepatocyte cell cycle via HGF activation in murine liver regeneration , 2005, Hepatology.

[37]  D. Stolz,et al.  Extracellular matrix remodeling at the early stages of liver regeneration in the rat , 1997, Hepatology.

[38]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[39]  F. Villarreal,et al.  Cardiac hypertrophy-induced changes in mRNA levels for TGF-beta 1, fibronectin, and collagen. , 1992, The American journal of physiology.

[40]  A. Kato,et al.  Relationship between expression of cyclin D1 and impaired liver regeneration observed in fibrotic or cirrhotic rats , 2005, Journal of gastroenterology and hepatology.

[41]  H. Mehendale,et al.  Stimulated hepatic tissue repair underlies heteroprotection by thioacetamide against acetaminophen‐induced lethality , 1995, Hepatology.

[42]  T. Morimoto,et al.  Absence of mitochondrial enhancement in the remnant liver after partial hepatectomy in cirrhotic rats , 1992, Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie.

[43]  M. Miyamoto,et al.  Characteristics of lectin staining patterns assessed by a modified sensitive thermo-method in rat livers with heterologous serum-induced fibrosis. , 1998, The Journal of veterinary medical science.

[44]  R. Hernández-Muñoz,et al.  Adenosine reverses a preestablished CCl4‐induced micronodular cirrhosis through enhancing collagenolytic activity and stimulating hepatocyte cell proliferation in rats , 2001, Hepatology.

[45]  M. Menger,et al.  Microvascular consequences of Kupffer cell modulation in rat liver fibrogenesis , 1999, The Journal of pathology.

[46]  K. Washington,et al.  Liver regeneration is transiently impaired in urokinase-deficient mice. , 1998, American journal of physiology. Gastrointestinal and liver physiology.

[47]  R. Hernández-Muñoz,et al.  Selective enhancement of lipid peroxidation in plasma membrane in two experimental models of liver regeneration: Partial hepatectomy and acute CCl4 administration , 1996, Hepatology.

[48]  M. Tanaka,et al.  Proliferating cell nuclear antigen, plasma fibronectin, and liver regeneration rate after seventy percent hepatectomy in normal and cirrhotic rats. , 1994, Surgery.

[49]  H. Kawaji,et al.  Decreased collagen accumulation by a prolyl hydroxylase inhibitor in pig serum‐induced fibrotic rat liver , 1988, Hepatology.

[50]  S. Friedman Molecular Regulation of Hepatic Fibrosis, an Integrated Cellular Response to Tissue Injury* , 2000, The Journal of Biological Chemistry.

[51]  M. Rojkind,et al.  In vivo collagen synthesis and deposition in fibrotic and regenerating rat livers. , 1983, Collagen and related research.

[52]  M. Arthur Fibrogenesis II. Metalloproteinases and their inhibitors in liver fibrosis. , 2000, American journal of physiology. Gastrointestinal and liver physiology.

[53]  M. Imamura,et al.  Portal branch ligation with a continuous hepatocyte growth factor supply makes extensive hepatectomy possible in cirrhotic rats , 1998, Hepatology.

[54]  S. Krane,et al.  Mutation in collagen‐I that confers resistance to the action of collagenase results in failure of recovery from CCl4‐induced liver fibrosis, persistence of activated hepatic stellate cells, and diminished hepatocyte regeneration , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[55]  Z. Werb,et al.  The many faces of metalloproteases: cell growth, invasion, angiogenesis and metastasis. , 2001, Trends in cell biology.

[56]  H. Popper,et al.  Chronic liver injury induced by immunologic reactions. Cirrhosis following immunization with heterologous sera. , 1966, The American journal of pathology.