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Immunohistochemical distribution of activated nuclear factor κB and peroxisome proliferator-activated receptors in carbon tetrachloride-induced chronic liver injury in rats

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Abstract

We investigated the immunohistochemical distribution of active NF-κB p65 and peroxisome proliferator-activated receptor (PPAR) subtypes alpha and gamma in the different phases of liver steatonecrosis and cirrhosis induced in rats after 3 and 9 weeks of carbon tetrachloride (CCl4) intoxication. CCl4 treatment can induce changes in the expression of NF-κB and PPARs. Immunohistochemical analysis of liver tissue sections from rats with steatonecrosis or cirrhosis demonstrated a significant increase in the number of NF-κB-positive and TNF-α-positive hepatocytes and Kupffer cells. In healthy controls, no expression of active NF-κB was detected. In previous studies, we have demonstrated that Kupffer cells isolated from rats with CCl4-induced steatonecrosis produced more reactive oxygen intermediates than cells isolated from normal rats. These oxidants could activate NF-κB and lead to an overexpression of TNF-α, observed in liver tissue sections. After CCl4 ingestion, the rat livers demonstrated a significantly decreased number of hepatocytes expressing PPARα and PPARγ and a significantly increased number of ED2-positive Kupffer cells expressing these transcription factors, compared to normal. The activation of the p65 isoform of NF-κB correlates negatively with transcription of the alpha and gamma isoforms of PPAR in hepatocytes, and positively in Kupffer cells. These results suggest that the regulation and the role of these two transcription factors differ in the two cell types studied.

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References

  • Alric L, Pinelli E, Carrera G, Vinel J, Beraud M, Duffaut M, Pascal JP, Pipy B (1996) Involvement of calcium in macrophage leukotriene release during experimental cirrhosis. Hepatology 23:614–622

    CAS  PubMed  Google Scholar 

  • Alric L, Orfila C, Carrere N, Beraud M, Carrera G, Lepert JC, Duffaut M, Pipy B, Vinel JP (2000) Reactive oxygen intermediates and eicosanoid production by Kupffer cells and infiltrated macrophages in acute and chronic liver injury induced in rats by CCl4. Inflamm Res 49:700–707

    Article  CAS  PubMed  Google Scholar 

  • Angermuller S, Fahimi HD (1988) Heterogenous staining of d-amino acid oxidase in peroxisomes of rat liver and kidney. A light and electron microscopic study. Histochemistry 88:277–285

    CAS  PubMed  Google Scholar 

  • Armendariz-Borunda J, Seyer JM, Postlethwaite AE, Kang AH (1991) Kupffer cells from carbon tetrachloride-injured rat livers produce chemotactic factors for fibroblasts and monocytes: the role of tumor necrosis factor-α. Hepatology 14:895–900

    CAS  PubMed  Google Scholar 

  • Auboeuf D, Rieusset J, Fajas L, Vallier P, Frering V, Riou JP, Staels B, Auwerx J, Laville M, Vidal H (1997) Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-α in humans. Diabetes 46:1319–1327

    CAS  PubMed  Google Scholar 

  • Auwerx J, Martin G, Guerre-Milo M, Staels B (1996) Transcription adipocyte differentiation and obesity. J Molec Med 74:347–352

    Article  CAS  Google Scholar 

  • Beier K, Volki A, Fahimi HD (1997) TNF-alpha downregulates the peroxisome proliferator activated receptor-alpha and the mRNAs encoding peroxisomal proteins in rat liver. FEBS Lett 412:385–387

    Article  CAS  PubMed  Google Scholar 

  • Braissant O, Foufelle F, Scotto C, Dauça M, Wahli W (1996) Differential expression of peroxisome proliferator-activated receptors (PPARs): tissue distribution of PPAR-α, -β, -γ in the adult rat. Endocrinology 137:354–366

    Article  CAS  PubMed  Google Scholar 

  • Burr AW, Carpenter MR, Hines JE, Gullick WJ, Burt AD (1993) Intrahepatic distribution of transforming growth factor-alpha (TGF alpha) during liver regeneration following carbon tetrachloride-induced necrosis. J Pathol 170:95–100

    CAS  PubMed  Google Scholar 

  • Chinetti G, Lestavel S, Bocher V, Remaley AT, Neve B, Torra IP, Teissier E, Minnich A, Jaye M, Duverger N, Bewer HB, Fruchart JC, Clavey V, Staels B (2001) PPAR-alpha and PPAR-gamma activators induce cholesterol removal from human macrophage foam cells through stimulation of the ABCA1 pathway. Nat Med 7:53–58

    Article  CAS  PubMed  Google Scholar 

  • Chung SW, Kang BY, Kim SH, Kim YM, Cho D, Trinchieri G, Kim TS (2000) Oxidized low density lipoprotein inhibits interleukin-12 production in lipopolysaccharide-activated mouse macrophages via direct interactions between PPARγ and NF-κB. J Biol Chem 276:32861–32867

    Google Scholar 

  • Davies GF, Khandelwal RL, Roesler WJ (1999) Troglitazone induces expression of PPARγ in liver. Mol Cell Biol Res Commun 2:202–208

    Google Scholar 

  • Delerive P, De Bosscher K, Besnard S, Vanden Berghe W, Peters JM, Gonzalez FJ, Fruchart JC, Tedgui A, Haegeman G, Staels B (1999) Peroxisome proliferator-activated receptor α negatively regulates the vascular inflammatory gene response by negative cross-talk with transcription factors NF-κB and AP-1. J Biol Chem 274:32048–32054

    Google Scholar 

  • ElSisi AE, Hall P, Sim WL, Earnest DL, Sipes IG (1993) Characterization of vitamin A potentiation of carbon tetrachloride-induced liver injury. Toxicol Appl Pharmacol 119:280–288

    Article  CAS  Google Scholar 

  • Everett L, Galli A, Crabb D (2000) The role of hepatic peroxisome proliferator-activated receptors (PPARs) in health and disease. Liver 20:191–199

    Article  CAS  Google Scholar 

  • Gossart S, Cambon C, Orfila C, Seguélas MH, Lepert JC, Rami J, Carré P, Pipy B (1996) Reactive oxygen intermediates as regulators of TNF-α production in rat lung inflammation induced by silica. J Immunol 156:1540–1548

    CAS  Google Scholar 

  • Hu E, Tontonoz P, Spiegelman BM (1995) Transdifferentiation of myoblasts by the adipocyte transcription factors PPAR gamma and C/EBP alpha. Proc Natl Acad Sci 92:9856–9860

    CAS  Google Scholar 

  • Huang Q, Yeldandi AV, Alvares K, Ide H, Reddy JK, Rao MS (1995) Localization of peroxisome proliferator-activated receptor in mouse and rat tissues and demonstration of its nuclear translocation in transfected CV-1 cells. Int J Oncol 6:307–312

    Google Scholar 

  • Imuro Y, Frankenberg MV, Arteel GE, Bradford BU, Wall CA, Thurman RG (1997) Female rats exhibit greater susceptibility to early alcohol-induced injury than males. Am J Physiol Gastrointest Liver Physiol 272:G1186–G1194

    Google Scholar 

  • Ip E, Farrell G, Robertson G, Leclercq I (2004) Administration of the potent PPARalpha agonist, WY-14,643, reverses nutritional fibrosis and steatohepatitis in mice. Hepatology 39:1286–1296

    Article  CAS  Google Scholar 

  • Jiang C, Ting AT, Seed B (1998) PPAR-γ agonists inhibit production of monocyte inflammatory cytokines. Nature 391:82–86

    Article  CAS  Google Scholar 

  • Johnson SJ, Hines JE, Burt AD (1992) Macrophage and perisinusoidal cell kinetics in acute liver injury. J Pathol 166:351–358

    CAS  Google Scholar 

  • Kon K, Ikejima K, Hirose M, Yoshikawa M, Enomoto N, Kitamura T, Takei Y, Sato N (2002) Pioglitazone prevents early-phase hepatic fibrogenesis caused by carbon tetrachloride. Biochem Biophys Res Commun 15:55–61

    Article  Google Scholar 

  • Lemberger T, Braissant O, Juge-Aubry C, Keller H, Saladin R, Staels B, Auwerx J, Burger AG, Meier CA, Wahli W (1996) PPAR tissue distribution and interactions with other hormone-signaling pathways. Ann N Y Acad Sci 804:231–251

    CAS  Google Scholar 

  • Loud AV (1968) A quantitative stereological description of the ultrastructure of normal rat liver parenchymal cells. J Cell Biol 37:27–46

    Article  CAS  Google Scholar 

  • Malapel M, Dharancy S, Roskams T, Auwerx J, Mathurin P, Desreumaux P (2004) Anti-inflammatory effects of peroxysome proliferator-activated receptor gamma in CCl4-induces hepatitis. Mediators Inflamm 13:62

    Google Scholar 

  • Marx N, Sukhova G, Murphy C, Libby P, Plutzky J (1998) Macrophages in human atheroma contain PPARγ. Am J Pathol 153:17–23

    CAS  Google Scholar 

  • Moller DE, Berger JP (2003) Role of PPARs in the regulation of obesity-related insulin sensitivity and inflammation. Int J Obes Relat Metab Disord 27(Suppl 3):S17–21

    Article  CAS  Google Scholar 

  • Mukherjee R, Jow L, Noonan D, McDonnell D (1994) Human and rat peroxisome proliferator activated receptors (PPARs) demonstrate similar tissue distribution but different responsiveness to PPAR activators. J Steroid Biochem Mol Biol 51:157–166

    Article  CAS  Google Scholar 

  • Neve BP, Fruchart J, Staels B (2000) Role of the peroxisome proliferator-activated receptors (PPAR) in atheroscleosis. Biochem Pharmacol 60:1245–1250

    Article  CAS  Google Scholar 

  • Orfila C, Lepert JC, Gossart S, Frisach MF, Cambon C, Pipy B (1998) Immunocytochemical characterization of lung macrophage surface phenotypes and expression of cytokines in acute experimental silicosis in mice. Histochem J 30:857–867

    Article  CAS  Google Scholar 

  • Orfila C, Lepert JC, Alric L, Carrera G, Beraud M, Vinel JP, Pipy B (1999) Expression of TNF-alpha and immunohistochemical distribution of hepatic macrophage surface markers in carbon tetrachloride-induced chronic liver injury in rats. Histochem J 31:677–685

    Article  CAS  Google Scholar 

  • Peters JM, Rusyn I, Rose ML, Gonzalez FJ, Thurman G (2000) Peroxisome proliferator-activated receptor α is restricted to hepatic parenchymal cells, not Kupffer cells: implications for the mechanism of action of peroxisome proliferators in hepatocarcinogenesis. Carcinogenesis 21:823–826

    Article  CAS  PubMed  Google Scholar 

  • Poynter ME, Daynes RA (1998) Peroxisome proliferator-activated receptor α activation modulates cellular redox status, represses nuclear factor-κB signaling, and reduces inflammatory cytokine production in aging. J Biol Chem 49:32833–32841

    Article  Google Scholar 

  • Proctor E, Chatamra K (1982) High yield micronodular cirrhosis in the rat. Gastroenterology 83:1183–1190

    CAS  Google Scholar 

  • Rao MS, Papreddy K, Musunuri S, Okonkwo A (2002) Preventional/reversal of choline deficiency-induced steatohepatitis by a peroxisome proliferator-activated receptor alpha ligand in rats. In vivo 16:145–152

    CAS  PubMed  Google Scholar 

  • Ricote M, Li AC, Willson TM, Kelly CJ, Glass CK (1998) The peroxisome proliferator-activated receptor-gamma is a negative regulator of macrophage activation. Nature 391:79–82

    Article  CAS  PubMed  Google Scholar 

  • Rusyn I, Rose ML, Bojes HK, Thurman RG (2000) Novel role of oxidants in the molecular mechanism of action of peroxisome proliferators. Antiox Redox Signal 2:607–621

    Article  CAS  Google Scholar 

  • Schreck R, Albermann KAJ, Baeurle PA (1992) Nuclear factor kappa B: an oxidative stress-responsive transcription factor of eukariotic cells (a review). Free Radic Res Commun 17:221–237

    CAS  PubMed  Google Scholar 

  • Sorensen HN, Treuter E, Gustafsson JA (1998) Regulation of peroxisome proliferator-activated receptors. Vitam Horm 54:121–126

    CAS  PubMed  Google Scholar 

  • Spencer NF, Poynter ME, Im SY, Daynes RA (1997) Constitutive activation of NF-kappa B in an animal model of aging. Int Immunol 9:1581–1588

    CAS  PubMed  Google Scholar 

Download references

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Correspondence to Claudine Orfila.

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Orfila, C., Lepert, JC., Alric, L. et al. Immunohistochemical distribution of activated nuclear factor κB and peroxisome proliferator-activated receptors in carbon tetrachloride-induced chronic liver injury in rats. Histochem Cell Biol 123, 585–593 (2005). https://doi.org/10.1007/s00418-005-0785-2

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