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Published in: Comparative Hepatology 1/2004

Open Access 01-01-2004 | Research

Heat shock protein 70 expression, keratin phosphorylation and Mallory body formation in hepatocytes from griseofulvin-intoxicated mice

Authors: Michel Fausther, Louis Villeneuve, Monique Cadrin

Published in: Comparative Hepatology | Issue 1/2004

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Abstract

Background

Keratins are members of the intermediate filaments (IFs) proteins, which constitute one of the three major cytoskeletal protein families. In hepatocytes, keratin 8 and 18 (K8/18) are believed to play a protective role against mechanical and toxic stress. Post-translational modifications such as phosphorylation and glycosylation are thought to modulate K8/18 functions. Treatment of mouse with a diet containing griseofulvin (GF) induces, in hepatocytes, modifications in organization, expression and phosphorylation of K8/18 IFs and leads, on the long term, to the formation of K8/18 containing aggregates morphologically and biochemically identical to Mallory bodies present in a number of human liver diseases. The aim of the present study was to investigate the relationship between the level and localization of the stress inducible heat shock protein 70 kDa (HSP70i) and the level and localization of K8/18 phosphorylation in the liver of GF-intoxicated mice. The role of these processes in Mallory body formation was studied, too. The experiment was carried out parallely on two different mouse strains, C3H and FVB/n.

Results

GF-treatment induced an increase in HSP70i expression and K8 phosphorylation on serines 79 (K8 S79), 436 (K8 S436), and K18 phosphorylation on serine 33 (K18 S33) as determined by Western blotting. Using immunofluorescence staining, we showed that after treatment, HSP70i was present in all hepatocytes. However, phosphorylated K8 S79 (K8 pS79) and K8 S436 (K8 pS436) were observed only in groups of hepatocytes or in isolated hepatocytes. K18 pS33 was increased in all hepatocytes. HSP70i colocalized with MBs containing phosphorylated K8/18. Phophorylation of K8 S79 was observed in C3H mice MBs but was not present in FVB/n MBs.

Conclusions

Our results indicate that GF intoxication represents a stress condition affecting all hepatocytes, whereas induction of K8/18 phosphorylation is not occurring in every hepatocyte. We conclude that, in vivo, there is no direct relationship between GF-induced stress and K8/18 phosphorylation on the studied sites. The K8/18 phosphorylation pattern indicates that different cell signaling pathways are activated in subpopulations of hepatocytes. Moreover, our results demonstrate that, in distinct genetic backgrounds, the induction of K8/18 phosphorylation can be different.
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Literature
1.
go back to reference Lazarides E: Intermediate filaments as mechanical integrators of cellular space. Nature. 1980, 283: 249-256.CrossRefPubMed Lazarides E: Intermediate filaments as mechanical integrators of cellular space. Nature. 1980, 283: 249-256.CrossRefPubMed
2.
go back to reference Fuchs E, Weber K: Intermediate filaments: structure, dynamics, function, and disease. Annu Rev Biochem. 1994, 63: 345-382.CrossRefPubMed Fuchs E, Weber K: Intermediate filaments: structure, dynamics, function, and disease. Annu Rev Biochem. 1994, 63: 345-382.CrossRefPubMed
3.
go back to reference Schliwa M: The cytoskeleton: An introductory survey. In : Alfert M, Beerman W, Goldstein L, Porter K R, eds Cell Biology Monograhs. Edited by: Springer-Verlag. 1986, New York, Wien, 13: Schliwa M: The cytoskeleton: An introductory survey. In : Alfert M, Beerman W, Goldstein L, Porter K R, eds Cell Biology Monograhs. Edited by: Springer-Verlag. 1986, New York, Wien, 13:
4.
go back to reference Herrmann H, Hesse M, Reichenzeller M, Aebi U, Magin TM: Functional complexity of intermediate filament cytoskeletons: from structure to assembly to gene ablation. Int Rev Cytol. 2003, 223: 83-175.CrossRefPubMed Herrmann H, Hesse M, Reichenzeller M, Aebi U, Magin TM: Functional complexity of intermediate filament cytoskeletons: from structure to assembly to gene ablation. Int Rev Cytol. 2003, 223: 83-175.CrossRefPubMed
5.
go back to reference Steinert PM, Roop DR: Molecular and cellular biology of intermediate filaments. Annu Rev Biochem. 1988, 57: 593-625. 10.1146/annurev.bi.57.070188.003113.CrossRefPubMed Steinert PM, Roop DR: Molecular and cellular biology of intermediate filaments. Annu Rev Biochem. 1988, 57: 593-625. 10.1146/annurev.bi.57.070188.003113.CrossRefPubMed
6.
go back to reference Moll R, Franke WW, Schiller DL, Geiger B, Krepler R: The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells. Cell. 1982, 31: 11-24. 10.1016/0092-8674(82)90400-7.CrossRefPubMed Moll R, Franke WW, Schiller DL, Geiger B, Krepler R: The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells. Cell. 1982, 31: 11-24. 10.1016/0092-8674(82)90400-7.CrossRefPubMed
7.
go back to reference Vassar R, Coulombe PA, Degenstein L, Albers K, Fuchs E: Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease. Cell. 1991, 64: 365-380. 10.1016/0092-8674(91)90645-F.CrossRefPubMed Vassar R, Coulombe PA, Degenstein L, Albers K, Fuchs E: Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease. Cell. 1991, 64: 365-380. 10.1016/0092-8674(91)90645-F.CrossRefPubMed
8.
go back to reference Fuchs E, Cleveland DW: A structural scaffolding of intermediate filaments in health and disease. Science. 1998, 279: 514-519. 10.1126/science.279.5350.514.CrossRefPubMed Fuchs E, Cleveland DW: A structural scaffolding of intermediate filaments in health and disease. Science. 1998, 279: 514-519. 10.1126/science.279.5350.514.CrossRefPubMed
9.
go back to reference Coulombe PA, Omary MB: 'Hard' and 'soft' principles defining the structure, function and regulation of keratin intermediate filaments. Curr Opin Cell Biol. 2002, 14: 110-122. 10.1016/S0955-0674(01)00301-5.CrossRefPubMed Coulombe PA, Omary MB: 'Hard' and 'soft' principles defining the structure, function and regulation of keratin intermediate filaments. Curr Opin Cell Biol. 2002, 14: 110-122. 10.1016/S0955-0674(01)00301-5.CrossRefPubMed
10.
go back to reference Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E: Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses. Cell. 1991, 66: 1301-1311. 10.1016/0092-8674(91)90051-Y.CrossRefPubMed Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E: Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses. Cell. 1991, 66: 1301-1311. 10.1016/0092-8674(91)90051-Y.CrossRefPubMed
11.
go back to reference Porter RM, Lane EB: Phenotypes, genotypes and their contribution to understanding keratin function. Trends Genet. 2003, 19: 278-285. 10.1016/S0168-9525(03)00071-4.CrossRefPubMed Porter RM, Lane EB: Phenotypes, genotypes and their contribution to understanding keratin function. Trends Genet. 2003, 19: 278-285. 10.1016/S0168-9525(03)00071-4.CrossRefPubMed
12.
go back to reference Loranger A, Duclos S, Grenier A, Price J, Wilson-Heiner M, Baribault H, Marceau N: Simple epithelium keratins are required for maintenance of hepatocyte integrity. Am J Pathol. 1997, 151: 1673-1683.PubMedCentralPubMed Loranger A, Duclos S, Grenier A, Price J, Wilson-Heiner M, Baribault H, Marceau N: Simple epithelium keratins are required for maintenance of hepatocyte integrity. Am J Pathol. 1997, 151: 1673-1683.PubMedCentralPubMed
13.
go back to reference Ku NO, Michie S, Oshima RG, Omary MB: Chronic hepatitis, hepatocyte fragility, and increased soluble phosphoglycokeratins in transgenic mice expressing a keratin 18 conserved arginine mutant. J Cell Biol. 1995, 131: 1303-1314. 10.1083/jcb.131.5.1303.CrossRefPubMed Ku NO, Michie S, Oshima RG, Omary MB: Chronic hepatitis, hepatocyte fragility, and increased soluble phosphoglycokeratins in transgenic mice expressing a keratin 18 conserved arginine mutant. J Cell Biol. 1995, 131: 1303-1314. 10.1083/jcb.131.5.1303.CrossRefPubMed
14.
go back to reference Ku NO, Darling JM, Krams SM, Esquivel CO, Keeffe EB, Sibley RK, Lee YM, Wright TL, Omary MB: Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. Proc Natl Acad Sci U S A. 2003, 100: 6063-6068. 10.1073/pnas.0936165100.PubMedCentralCrossRefPubMed Ku NO, Darling JM, Krams SM, Esquivel CO, Keeffe EB, Sibley RK, Lee YM, Wright TL, Omary MB: Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. Proc Natl Acad Sci U S A. 2003, 100: 6063-6068. 10.1073/pnas.0936165100.PubMedCentralCrossRefPubMed
15.
go back to reference Ku NO, Gish R, Wright TL, Omary MB: Keratin 8 mutations in patients with cryptogenic liver disease. N Engl J Med. 2001, 344: 1580-1587. 10.1056/NEJM200105243442103.CrossRefPubMed Ku NO, Gish R, Wright TL, Omary MB: Keratin 8 mutations in patients with cryptogenic liver disease. N Engl J Med. 2001, 344: 1580-1587. 10.1056/NEJM200105243442103.CrossRefPubMed
16.
go back to reference Ku NO, Wright TL, Terrault NA, Gish R, Omary MB: Mutation of human keratin 18 in association with cryptogenic cirrhosis. J Clin Invest. 1997, 99: 19-23.PubMedCentralCrossRefPubMed Ku NO, Wright TL, Terrault NA, Gish R, Omary MB: Mutation of human keratin 18 in association with cryptogenic cirrhosis. J Clin Invest. 1997, 99: 19-23.PubMedCentralCrossRefPubMed
17.
go back to reference Denk H, Krepler R, Lackinger E, Artlieb U, Franke WW: Immunological and biochemical characterization of the keratin-related component of Mallory bodies: a pathological pattern of hepatocytic cytokeratins. Liver. 1982, 2: 165-175.CrossRefPubMed Denk H, Krepler R, Lackinger E, Artlieb U, Franke WW: Immunological and biochemical characterization of the keratin-related component of Mallory bodies: a pathological pattern of hepatocytic cytokeratins. Liver. 1982, 2: 165-175.CrossRefPubMed
18.
go back to reference Hazan R, Denk H, Franke WW, Lackinger E, Schiller DL: Change of cytokeratin organization during development of Mallory bodies as revealed by a monoclonal antibody. Lab Invest. 1986, 54: 543-553.PubMed Hazan R, Denk H, Franke WW, Lackinger E, Schiller DL: Change of cytokeratin organization during development of Mallory bodies as revealed by a monoclonal antibody. Lab Invest. 1986, 54: 543-553.PubMed
19.
go back to reference Jensen K, Gluud C: The Mallory body: theories on development and pathological significance (Part 2 of a literature survey). Hepatology. 1994, 20: 1330-1342. 10.1016/0270-9139(94)90776-5.CrossRefPubMed Jensen K, Gluud C: The Mallory body: theories on development and pathological significance (Part 2 of a literature survey). Hepatology. 1994, 20: 1330-1342. 10.1016/0270-9139(94)90776-5.CrossRefPubMed
20.
go back to reference Jensen K, Gluud C: The Mallory body: morphological, clinical and experimental studies (Part 1 of a literature survey). Hepatology. 1994, 20: 1061-1077. 10.1016/0270-9139(94)90776-5.CrossRefPubMed Jensen K, Gluud C: The Mallory body: morphological, clinical and experimental studies (Part 1 of a literature survey). Hepatology. 1994, 20: 1061-1077. 10.1016/0270-9139(94)90776-5.CrossRefPubMed
21.
go back to reference Denk H, Stumptner C, Zatloukal K: Mallory bodies revisited. J Hepatol. 2000, 32: 689-702. 10.1016/S0168-8278(00)80233-0.CrossRefPubMed Denk H, Stumptner C, Zatloukal K: Mallory bodies revisited. J Hepatol. 2000, 32: 689-702. 10.1016/S0168-8278(00)80233-0.CrossRefPubMed
22.
go back to reference Mayer R, Lowe J, Landon M, McDermott H, Tuckwell J, Doherty F, Laszlo L: Ubiquitin and the lysosome system: molecular pathological and experimental findings. Eds Maresca, B and Lindquist, S. Edited by: Springer-Verlag. 1991, New York, Heidelberg, pp. 299-314. Mayer R, Lowe J, Landon M, McDermott H, Tuckwell J, Doherty F, Laszlo L: Ubiquitin and the lysosome system: molecular pathological and experimental findings. Eds Maresca, B and Lindquist, S. Edited by: Springer-Verlag. 1991, New York, Heidelberg, pp. 299-314.
23.
go back to reference Yuan QX, Marceau N, French BA, Fu P, French SW: Heat shock in vivo induces Mallory body formation in drug primed mouse liver. Exp Mol Pathol. 1995, 63: 63-76. 10.1006/exmp.1995.1031.CrossRefPubMed Yuan QX, Marceau N, French BA, Fu P, French SW: Heat shock in vivo induces Mallory body formation in drug primed mouse liver. Exp Mol Pathol. 1995, 63: 63-76. 10.1006/exmp.1995.1031.CrossRefPubMed
24.
go back to reference Riley NE, Li J, McPhaul LW, Bardag-Gorce F, Lue YH, French SW: Heat shock proteins are present in mallory bodies (cytokeratin aggresomes) in human liver biopsy specimens. Exp Mol Pathol. 2003, 74: 168-172. 10.1016/S0014-4800(02)00020-5.CrossRefPubMed Riley NE, Li J, McPhaul LW, Bardag-Gorce F, Lue YH, French SW: Heat shock proteins are present in mallory bodies (cytokeratin aggresomes) in human liver biopsy specimens. Exp Mol Pathol. 2003, 74: 168-172. 10.1016/S0014-4800(02)00020-5.CrossRefPubMed
25.
go back to reference Liao J, Ku NO, Omary MB: Stress, apoptosis, and mitosis induce phosphorylation of human keratin 8 at Ser-73 in tissues and cultured cells. J Biol Chem. 1997, 272: 17565-17573. 10.1074/jbc.272.28.17565.CrossRefPubMed Liao J, Ku NO, Omary MB: Stress, apoptosis, and mitosis induce phosphorylation of human keratin 8 at Ser-73 in tissues and cultured cells. J Biol Chem. 1997, 272: 17565-17573. 10.1074/jbc.272.28.17565.CrossRefPubMed
26.
go back to reference Omary MB, Ku NO, Liao J, Price D: Keratin modifications and solubility properties in epithelial cells and in vitro. Subcell Biochem. 1998, 31: 105-140.PubMed Omary MB, Ku NO, Liao J, Price D: Keratin modifications and solubility properties in epithelial cells and in vitro. Subcell Biochem. 1998, 31: 105-140.PubMed
27.
go back to reference Toivola DM, Zhou Q, English LS, Omary MB: Type II keratins are phosphorylated on a unique motif during stress and mitosis in tissues and cultured cells. Mol Biol Cell. 2002, 13: 1857-1870. 10.1091/mbc.01-12-0591.PubMedCentralCrossRefPubMed Toivola DM, Zhou Q, English LS, Omary MB: Type II keratins are phosphorylated on a unique motif during stress and mitosis in tissues and cultured cells. Mol Biol Cell. 2002, 13: 1857-1870. 10.1091/mbc.01-12-0591.PubMedCentralCrossRefPubMed
28.
go back to reference Denk H, Gschnait F, Wolff K: Hepatocellar hyalin (Mallory bodies) in long term griseofulvin-treated mice: a new experimental model for the study of hyalin formation. Lab Invest. 1975, 32: 773-776.PubMed Denk H, Gschnait F, Wolff K: Hepatocellar hyalin (Mallory bodies) in long term griseofulvin-treated mice: a new experimental model for the study of hyalin formation. Lab Invest. 1975, 32: 773-776.PubMed
29.
go back to reference Ku NO, Zhou X, Toivola DM, Omary MB: The cytoskeleton of digestive epithelia in health and disease. Am J Physiol. 1999, 277: G1108-37.PubMed Ku NO, Zhou X, Toivola DM, Omary MB: The cytoskeleton of digestive epithelia in health and disease. Am J Physiol. 1999, 277: G1108-37.PubMed
30.
go back to reference Baribault H, Penner J, Iozzo RV, Wilson-Heiner M: Colorectal hyperplasia and inflammation in keratin 8-deficient FVB/N mice. Genes Dev. 1994, 8: 2964-2973.CrossRefPubMed Baribault H, Penner J, Iozzo RV, Wilson-Heiner M: Colorectal hyperplasia and inflammation in keratin 8-deficient FVB/N mice. Genes Dev. 1994, 8: 2964-2973.CrossRefPubMed
31.
go back to reference Baribault H, Price J, Miyai K, Oshima RG: Mid-gestational lethality in mice lacking keratin 8. Genes Dev. 1993, 7: 1191-1202.CrossRefPubMed Baribault H, Price J, Miyai K, Oshima RG: Mid-gestational lethality in mice lacking keratin 8. Genes Dev. 1993, 7: 1191-1202.CrossRefPubMed
32.
go back to reference Gilbert S, Loranger A, Daigle N, Marceau N: Simple epithelium keratins 8 and 18 provide resistance to Fas-mediated apoptosis. The protection occurs through a receptor-targeting modulation. J Cell Biol. 2001, 154: 763-773. 10.1083/jcb.200102130.PubMedCentralCrossRefPubMed Gilbert S, Loranger A, Daigle N, Marceau N: Simple epithelium keratins 8 and 18 provide resistance to Fas-mediated apoptosis. The protection occurs through a receptor-targeting modulation. J Cell Biol. 2001, 154: 763-773. 10.1083/jcb.200102130.PubMedCentralCrossRefPubMed
33.
go back to reference Cadrin M, Hovington H, Marceau N, McFarlane-Anderson N: Early perturbations in keratin and actin gene expression and fibrillar organisation in griseofulvin-fed mouse liver. J Hepatol. 2000, 33: 199-207. 10.1016/S0168-8278(00)80360-8.CrossRefPubMed Cadrin M, Hovington H, Marceau N, McFarlane-Anderson N: Early perturbations in keratin and actin gene expression and fibrillar organisation in griseofulvin-fed mouse liver. J Hepatol. 2000, 33: 199-207. 10.1016/S0168-8278(00)80360-8.CrossRefPubMed
34.
go back to reference Marceau N, Loranger A, Gilbert S, Daigle N, Champetier S: Keratin-mediated resistance to stress and apoptosis in simple epithelial cells in relation to health and disease. Biochem Cell Biol. 2001, 79: 543-555. 10.1139/bcb-79-5-543.CrossRefPubMed Marceau N, Loranger A, Gilbert S, Daigle N, Champetier S: Keratin-mediated resistance to stress and apoptosis in simple epithelial cells in relation to health and disease. Biochem Cell Biol. 2001, 79: 543-555. 10.1139/bcb-79-5-543.CrossRefPubMed
35.
go back to reference Omary MB, Ku NO, Toivola DM: Keratins: guardians of the liver. Hepatology. 2002, 35: 251-257. 10.1053/jhep.2002.31165.CrossRefPubMed Omary MB, Ku NO, Toivola DM: Keratins: guardians of the liver. Hepatology. 2002, 35: 251-257. 10.1053/jhep.2002.31165.CrossRefPubMed
36.
go back to reference Ku NO, Omary MB: Expression, glycosylation, and phosphorylation of human keratins 8 and 18 in insect cells. Exp Cell Res. 1994, 211: 24-35. 10.1006/excr.1994.1054.CrossRefPubMed Ku NO, Omary MB: Expression, glycosylation, and phosphorylation of human keratins 8 and 18 in insect cells. Exp Cell Res. 1994, 211: 24-35. 10.1006/excr.1994.1054.CrossRefPubMed
37.
go back to reference Ku NO, Azhar S, Omary MB: Keratin 8 phosphorylation by p38 kinase regulates cellular keratin filament reorganization: modulation by a keratin 1-like disease causing mutation. J Biol Chem. 2002, 277: 10775-10782. 10.1074/jbc.M107623200.CrossRefPubMed Ku NO, Azhar S, Omary MB: Keratin 8 phosphorylation by p38 kinase regulates cellular keratin filament reorganization: modulation by a keratin 1-like disease causing mutation. J Biol Chem. 2002, 277: 10775-10782. 10.1074/jbc.M107623200.CrossRefPubMed
38.
go back to reference Liao J, Lowthert LA, Omary MB: Heat stress or rotavirus infection of human epithelial cells generates a distinct hyperphosphorylated form of keratin 8. Exp Cell Res. 1995, 219: 348-357. 10.1006/excr.1995.1238.CrossRefPubMed Liao J, Lowthert LA, Omary MB: Heat stress or rotavirus infection of human epithelial cells generates a distinct hyperphosphorylated form of keratin 8. Exp Cell Res. 1995, 219: 348-357. 10.1006/excr.1995.1238.CrossRefPubMed
39.
go back to reference Ku NO, Liao J, Chou CF, Omary MB: Implications of intermediate filament protein phosphorylation. Cancer Metastasis Rev. 1996, 15: 429-444.CrossRefPubMed Ku NO, Liao J, Chou CF, Omary MB: Implications of intermediate filament protein phosphorylation. Cancer Metastasis Rev. 1996, 15: 429-444.CrossRefPubMed
40.
go back to reference Ku NO, Michie SA, Soetikno RM, Resurreccion EZ, Broome RL, Omary MB: Mutation of a major keratin phosphorylation site predisposes to hepatotoxic injury in transgenic mice. J Cell Biol. 1998, 143: 2023-2032. 10.1083/jcb.143.7.2023.PubMedCentralCrossRefPubMed Ku NO, Michie SA, Soetikno RM, Resurreccion EZ, Broome RL, Omary MB: Mutation of a major keratin phosphorylation site predisposes to hepatotoxic injury in transgenic mice. J Cell Biol. 1998, 143: 2023-2032. 10.1083/jcb.143.7.2023.PubMedCentralCrossRefPubMed
41.
go back to reference Knasmuller S, Parzefall W, Helma C, Kassie F, Ecker S, Schulte-Hermann R: Toxic effects of griseofulvin: disease models, mechanisms, and risk assessment. Crit Rev Toxicol. 1997, 27: 495-537.CrossRefPubMed Knasmuller S, Parzefall W, Helma C, Kassie F, Ecker S, Schulte-Hermann R: Toxic effects of griseofulvin: disease models, mechanisms, and risk assessment. Crit Rev Toxicol. 1997, 27: 495-537.CrossRefPubMed
42.
go back to reference Stege GJ, Li L, Kampinga HH, Konings AW, Li GC: Importance of the ATP-binding domain and nucleolar localization domain of HSP72 in the protection of nuclear proteins against heat-induced aggregation. Exp Cell Res. 1994, 214: 279-284. 10.1006/excr.1994.1259.CrossRefPubMed Stege GJ, Li L, Kampinga HH, Konings AW, Li GC: Importance of the ATP-binding domain and nucleolar localization domain of HSP72 in the protection of nuclear proteins against heat-induced aggregation. Exp Cell Res. 1994, 214: 279-284. 10.1006/excr.1994.1259.CrossRefPubMed
43.
go back to reference Welch WJ, Feramisco JR: Nuclear and nucleolar localization of the 72,000-dalton heat shock protein in heat-shocked mammalian cells. J Biol Chem. 1984, 259: 4501-4513.PubMed Welch WJ, Feramisco JR: Nuclear and nucleolar localization of the 72,000-dalton heat shock protein in heat-shocked mammalian cells. J Biol Chem. 1984, 259: 4501-4513.PubMed
44.
go back to reference Kawahara H, Cadrin M, French SW: Ethanol-induced phosphorylation of cytokeratin in cultured hepatocytes. Life Sci. 1990, 47: 859-863. 10.1016/0024-3205(90)90598-L.CrossRefPubMed Kawahara H, Cadrin M, French SW: Ethanol-induced phosphorylation of cytokeratin in cultured hepatocytes. Life Sci. 1990, 47: 859-863. 10.1016/0024-3205(90)90598-L.CrossRefPubMed
45.
go back to reference Cadrin M, Anderson NM, Aasheim LH, Kawahara H, Franks DJ, French SW: Modifications in cytokeratin and actin in cultured liver cells derived from griseofulvin-fed mice. Lab Invest. 1995, 72: 453-460.PubMed Cadrin M, Anderson NM, Aasheim LH, Kawahara H, Franks DJ, French SW: Modifications in cytokeratin and actin in cultured liver cells derived from griseofulvin-fed mice. Lab Invest. 1995, 72: 453-460.PubMed
46.
go back to reference Ku NO, Liao J, Omary MB: Phosphorylation of human keratin 18 serine 33 regulates binding to 14-3-3 proteins. Embo J. 1998, 17: 1892-1906. 10.1093/emboj/17.7.1892.PubMedCentralCrossRefPubMed Ku NO, Liao J, Omary MB: Phosphorylation of human keratin 18 serine 33 regulates binding to 14-3-3 proteins. Embo J. 1998, 17: 1892-1906. 10.1093/emboj/17.7.1892.PubMedCentralCrossRefPubMed
47.
go back to reference Ku NO, Michie S, Resurreccion EZ, Broome RL, Omary MB: Keratin binding to 14-3-3 proteins modulates keratin filaments and hepatocyte mitotic progression. Proc Natl Acad Sci U S A. 2002, 99: 4373-4378. 10.1073/pnas.072624299.PubMedCentralCrossRefPubMed Ku NO, Michie S, Resurreccion EZ, Broome RL, Omary MB: Keratin binding to 14-3-3 proteins modulates keratin filaments and hepatocyte mitotic progression. Proc Natl Acad Sci U S A. 2002, 99: 4373-4378. 10.1073/pnas.072624299.PubMedCentralCrossRefPubMed
48.
go back to reference Ku NO, Omary MB: Phosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431. J Biol Chem. 1997, 272: 7556-7564. 10.1074/jbc.272.52.33197.CrossRefPubMed Ku NO, Omary MB: Phosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431. J Biol Chem. 1997, 272: 7556-7564. 10.1074/jbc.272.52.33197.CrossRefPubMed
49.
go back to reference Stumptner C, Omary MB, Fickert P, Denk H, Zatloukal K: Hepatocyte cytokeratins are hyperphosphorylated at multiple sites in human alcoholic hepatitis and in a mallory body mouse model. Am J Pathol. 2000, 156: 77-90.PubMedCentralCrossRefPubMed Stumptner C, Omary MB, Fickert P, Denk H, Zatloukal K: Hepatocyte cytokeratins are hyperphosphorylated at multiple sites in human alcoholic hepatitis and in a mallory body mouse model. Am J Pathol. 2000, 156: 77-90.PubMedCentralCrossRefPubMed
50.
go back to reference Liao J, Lowthert LA, Ghori N, Omary MB: The 70-kDa heat shock proteins associate with glandular intermediate filaments in an ATP-dependent manner. J Biol Chem. 1995, 270: 915-922. 10.1074/jbc.270.2.915.CrossRefPubMed Liao J, Lowthert LA, Ghori N, Omary MB: The 70-kDa heat shock proteins associate with glandular intermediate filaments in an ATP-dependent manner. J Biol Chem. 1995, 270: 915-922. 10.1074/jbc.270.2.915.CrossRefPubMed
51.
52.
go back to reference Gabai VL, Meriin AB, Mosser DD, Caron AW, Rits S, Shifrin VI, Sherman MY: Hsp70 prevents activation of stress kinases. A novel pathway of cellular thermotolerance. J Biol Chem. 1997, 272: 18033-18037. 10.1074/jbc.272.29.18033.CrossRefPubMed Gabai VL, Meriin AB, Mosser DD, Caron AW, Rits S, Shifrin VI, Sherman MY: Hsp70 prevents activation of stress kinases. A novel pathway of cellular thermotolerance. J Biol Chem. 1997, 272: 18033-18037. 10.1074/jbc.272.29.18033.CrossRefPubMed
53.
go back to reference Bardag-Gorce F, van Leeuwen FW, Nguyen V, French BA, Li J, Riley N, McPhaul LW, Lue YH, French SW: The role of the ubiquitin-proteasome pathway in the formation of mallory bodies. Exp Mol Pathol. 2002, 73: 75-83. 10.1006/exmp.2002.2451.CrossRefPubMed Bardag-Gorce F, van Leeuwen FW, Nguyen V, French BA, Li J, Riley N, McPhaul LW, Lue YH, French SW: The role of the ubiquitin-proteasome pathway in the formation of mallory bodies. Exp Mol Pathol. 2002, 73: 75-83. 10.1006/exmp.2002.2451.CrossRefPubMed
54.
go back to reference Stumptner C, Fuchsbichler A, Lehner M, Zatloukal K, Denk H: Sequence of events in the assembly of Mallory body components in mouse liver: clues to the pathogenesis and significance of Mallory body formation. J Hepatol. 2001, 34: 665-675. 10.1016/S0168-8278(00)00099-4.CrossRefPubMed Stumptner C, Fuchsbichler A, Lehner M, Zatloukal K, Denk H: Sequence of events in the assembly of Mallory body components in mouse liver: clues to the pathogenesis and significance of Mallory body formation. J Hepatol. 2001, 34: 665-675. 10.1016/S0168-8278(00)00099-4.CrossRefPubMed
55.
go back to reference He T, Stepulak A, Holmstrom TH, Omary MB, Eriksson JE: The intermediate filament protein keratin 8 is a novel cytoplasmic substrate for c-Jun N-terminal kinase. J Biol Chem. 2002, 277: 10767-10774. 10.1074/jbc.M111436200.CrossRefPubMed He T, Stepulak A, Holmstrom TH, Omary MB, Eriksson JE: The intermediate filament protein keratin 8 is a novel cytoplasmic substrate for c-Jun N-terminal kinase. J Biol Chem. 2002, 277: 10767-10774. 10.1074/jbc.M111436200.CrossRefPubMed
56.
go back to reference Boller K, Kemler R, Baribault H, Doetschman T: Differential distribution of cytokeratins after microinjection of anti-cytokeratin monoclonal antibodies. Eur J Cell Biol. 1987, 43: 459-468.PubMed Boller K, Kemler R, Baribault H, Doetschman T: Differential distribution of cytokeratins after microinjection of anti-cytokeratin monoclonal antibodies. Eur J Cell Biol. 1987, 43: 459-468.PubMed
57.
go back to reference Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970, 227: 680-685.CrossRefPubMed Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970, 227: 680-685.CrossRefPubMed
58.
go back to reference Lowry OH, Rosebrough NJ, Farr AL, Randall RJ: Protein measurement with the Phenol folin reagent. J Biol Chem. 1951, 193: 265-275.PubMed Lowry OH, Rosebrough NJ, Farr AL, Randall RJ: Protein measurement with the Phenol folin reagent. J Biol Chem. 1951, 193: 265-275.PubMed
Metadata
Title
Heat shock protein 70 expression, keratin phosphorylation and Mallory body formation in hepatocytes from griseofulvin-intoxicated mice
Authors
Michel Fausther
Louis Villeneuve
Monique Cadrin
Publication date
01-01-2004
Publisher
BioMed Central
Published in
Comparative Hepatology / Issue 1/2004
Electronic ISSN: 1476-5926
DOI
https://doi.org/10.1186/1476-5926-3-5

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