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1.
Exp Mol Pathol ; 103(2): 191-199, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28935395

RESUMO

Several research strategies have been used to study the pathogenesis of alcoholic hepatitis (AH). These strategies have shown that various signaling pathways are the target of alcohol in liver cells. However, few have provided specific mechanisms associated with Mallory-Denk Bodies (MDBs) formed in Balloon cells in AH. The formation of MDBs in these hepatocytes is an indication that the mechanisms of protein quality control have failed. The MDB is the result of aggregation and accumulation of proteins in the cytoplasm of balloon degenerated liver cells. To understand the mechanisms that failed to degrade and remove proteins in the hepatocyte from patients suffering from alcoholic hepatitis, we investigated the pathways that showed significant up regulation in the AH liver biopsies compared to normal control livers (Liu et al., 2015). Analysis of genomic profiles of AH liver biopsies and control livers by RNA-seq revealed different pathways that were up regulated significantly. In this study, the focus was on Tec kinase signaling pathways and the genes that significantly interrupt this pathway. Quantitative PCR and immunofluorescence staining results, indicated that several genes and proteins are significantly over expressed in the livers of AH patients that affect the Tec kinase signaling to PI3K which leads to activation of Akt and its downstream effectors.


Assuntos
Biomarcadores/metabolismo , Hepatite Alcoólica/patologia , Hepatócitos/patologia , Fígado/patologia , Corpos de Mallory/patologia , Proteínas Tirosina Quinases/metabolismo , Transdução de Sinais , Estudos de Casos e Controles , Perfilação da Expressão Gênica , Hepatite Alcoólica/metabolismo , Hepatócitos/metabolismo , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Fígado/metabolismo , Corpos de Mallory/metabolismo , Proteínas Tirosina Quinases/genética
2.
Exp Mol Pathol ; 103(2): 137-140, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28818508

RESUMO

BACKGROUND AND AIM: IL-8 (C-X-L motif chemokine ligase 8) and CXCR2 (C-X-C-motif chemokine receptor 2) are up regulated in alcoholic hepatitis (AH) liver biopsies. One of the consequences is the attraction and chemotactic neutrophilic infiltrate seen at the AH stage of alcoholic liver disease. MATERIALS AND METHODS: Human formalin-fixed, paraffin-embedded (FFPE) liver biopsies from patients who have AH were studied by (2.1) RNA sequencing, (2.2) PCR and (2.3) semi quantitation of specific proteins in biopsy sections using immunohistochemical measurements of antibody fluorescent intensity with morphometric technology. RESULTS: Immunohistochemistry of IL-8 showed that the expression was increased in the cytoplasm of the hepatocytes in AH liver biopsies compared to the controls. IL-8 and ubiquitin were co-localized in the MDBs. Numerous neutrophils were found throughout and satellitosis of neutrophils around MDBs was present. This suggested that IL-8 may be involved in MDB pathogenesis. RNA seq analysis revealed activation by IL-8 which included neutrophil chemotaxis by LIM domain kinase 2 (LIMK2) (17.5 fold increase) and G protein subunit alpha 15 (GNA15) (27.8 fold increase). CONCLUSIONS: The formation of MDBs by liver cells showed colocalization of ubiquitin and IL-8 in the MDBs. This suggested that IL-8 in these hepatocytes attracted the neutrophils to form satellitosis. This correlated with up regulation of the proteins downstream from the IL-8 pathways including LIMK2, GNG2 (guanine nucleotide binding proteins) and PIK3CB (phosphatidyl isitol-4, 5-biophosphate-3-kinase, catalytic subunit beta).


Assuntos
Biomarcadores/metabolismo , Granulócitos/imunologia , Hepatite Alcoólica/imunologia , Interleucina-8/metabolismo , Fígado/imunologia , Transdução de Sinais , Estudos de Casos e Controles , Granulócitos/metabolismo , Granulócitos/patologia , Hepatite Alcoólica/genética , Hepatite Alcoólica/metabolismo , Hepatite Alcoólica/patologia , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Interleucina-8/genética , Fígado/metabolismo , Fígado/patologia
3.
Exp Mol Pathol ; 102(1): 106-114, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-28089901

RESUMO

In this study, liver biopsy sections fixed in formalin and embedded in paraffin (FFPE) from patients with alcoholic hepatitis (AH) were used. The results showed that the expression of the SYK protein was up regulated by RNA-seq and real time PCR analyses in the alcoholic hepatitis patients compared to controls. The results were supported by using the IHC fluorescent antibody staining intensity morphometric quantitation. Morphometric quantification of fluorescent intensity measurement showed a two fold increase in SYK protein in the cytoplasm of the cells forming MDBs compared to surrounding normal hepatocytes. The expression of AKT1 was also analyzed. AKT1 is a serine/threonine-specific protein kinase that plays a key role in multiple cellular processes such as glucose metabolism, apoptosis, cell proliferation, transcription and cell migration. The AKT protein was also increased in hepatocyte balloon cells forming MDBs. This observation demonstrates the role of SYK and its subsequent effect on the internal signaling pathways such as PI3K/AKT as well as p70S6K, as a potential multifunctional target in protein quality control mechanisms of hepatocytes when ER stress is activated.


Assuntos
Citoplasma/metabolismo , Fígado/metabolismo , Corpos de Mallory/metabolismo , Proteínas Proto-Oncogênicas c-akt/biossíntese , Transdução de Sinais , Quinase Syk/biossíntese , Biópsia , Citoplasma/genética , Hepatite Alcoólica/genética , Hepatite Alcoólica/metabolismo , Hepatite Alcoólica/patologia , Hepatócitos/metabolismo , Humanos , Immunoblotting , Imuno-Histoquímica , Fígado/patologia , Fosfatidilinositol 3-Quinases/genética , Fosfatidilinositol 3-Quinases/metabolismo , Proteínas Proto-Oncogênicas c-akt/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Proteínas Quinases S6 Ribossômicas 70-kDa/genética , Proteínas Quinases S6 Ribossômicas 70-kDa/metabolismo , Quinase Syk/genética
5.
Exp Mol Pathol ; 101(1): 81-8, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27432584

RESUMO

There are many homeostatic mechanisms for coping with stress conditions in cells, including autophagy. In many studies autophagy, as an intracellular pathway which degrades misfolded and damaged protein, and Mallory-Denk Body (MDB) formation have been shown to be protective mechanisms against stress such as alcoholic hepatitis. Alcohol has a significant role in alteration of lipid homeostasis, sterol regulatory element-binding proteins (SREBPs) and peroxidase proliferator-activated receptors through AMP-activated protein kinase (AMPK)-dependent mechanism. AMPK is one of the kinases that regulate autophagy through the dephosphorylation of ATG1. Activation of ATG1 (ULK kinases family) activates ATG6. These two activated proteins relocate to the site of initial autophagosome and activate the other downstream components of autophagocytosis. Many other proteins regulate autophagocytosis at the gene level. CHOP (C/EBP homologous protein) is one of the most important parts of stress-inducible transcription that encodes a ubiquitous transcription factor. In this report we measure the upregulation of the gene that are involved in autophagocytosis in liver biopsies of alcoholic hepatitis and NASH. Electron microscopy was used to document the presence of autophagosomes in the liver cells. Expression of AMPK1, ATG1, ATG6 and CHOP in ASH were significantly (p value<0.05) upregulated in comparison to control. Electron microscopy findings of ASH confirmed the presence of autophagosomes, one of which contained a MDB, heretofore undescribed. Significant upregulations of AMPK-1, ATG-1, ATG-6, and CHOP, and uptrending of ATG-4, ATG-5, ATG-9, ATR, and ATM in ASH compared to normal control livers indicate active autophagocytosis in alcoholic hepatitis.


Assuntos
Autofagia , Hepatite Alcoólica/patologia , Hepatopatia Gordurosa não Alcoólica/patologia , Regulação para Cima , Proteínas Quinases Ativadas por AMP/metabolismo , Proteínas Relacionadas à Autofagia/metabolismo , Estudos de Casos e Controles , Hepatite Alcoólica/enzimologia , Humanos , Hepatopatia Gordurosa não Alcoólica/enzimologia , Fagossomos/metabolismo , Fagossomos/ultraestrutura
7.
Exp Mol Pathol ; 100(3): 426-33, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-27068270

RESUMO

There is a possibility that the aggresomes that form in the brain in neurodegenerative diseases like Alzheimer's disease (AD) and in the liver where aggresomes like Mallory-Denk Bodies (MDB) form, share mechanisms. MDBs can be prevented by feeding mice sadenosylmethionine (SAMe) or betaine. Possibly these proteins could prevent AD. We compared the literature on MDBs and AD pathogenesis, which include roles played by p62, ubiquitin UBB +1, HSPs70, 90, 104, FAT10, NEDD8, VCP/97, and the protein quality control mechanisms including the 26s proteasome, the IPOD and JUNQ and autophagosome pathways.


Assuntos
Doença de Alzheimer/metabolismo , Corpos de Mallory/metabolismo , Doenças Neurodegenerativas/metabolismo , Agregados Proteicos , Agregação Patológica de Proteínas/metabolismo , Animais , Autofagossomos/metabolismo , Humanos , Modelos Biológicos , Complexo de Endopeptidases do Proteassoma/metabolismo
8.
Exp Mol Pathol ; 98(2): 304-7, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25758202

RESUMO

Betaine supplements of alcoholic beverages are proposed to prevent the development of alcoholic liver disease in patients that abuse alcohol. This recommendation is based on the observation of studies where it has been shown in binge drinking and chronic ethanol feeding animal models that betaine prevents liver injury resulting from high blood alcohol levels. The basic observation is that betaine added to ethanol being ingested increases the elimination rate of blood alcohol, which prevents the blood alcohol levels (BALs) from reaching high levels. The mechanism of how betaine does this is postulated to be that betaine causes the increase in the elimination rate by increasing the metabolic rate which generates NAD the rate limiting cofactor of alcohol oxidation by ADH. Betaine does this most likely by supporting the methylation of norepinephrine to form epinephrine by phenylethanolamine N-methyltransferase. Epinephrine is 5 to 10-fold more active than norepinephrine in increasing the metabolic rate.


Assuntos
Betaína/uso terapêutico , Metabolismo Energético/efeitos dos fármacos , Etanol/sangue , Hepatopatias Alcoólicas/metabolismo , Hepatopatias Alcoólicas/prevenção & controle , Alcoolismo , Animais , Betaína/administração & dosagem , Epinefrina/biossíntese , Etanol/metabolismo , Humanos , Fígado/metabolismo , Metilação/efeitos dos fármacos , Modelos Animais , Norepinefrina/metabolismo , Oxirredução , Feniletanolamina N-Metiltransferase/metabolismo , Ratos
9.
Exp Mol Pathol ; 97(3): 399-410, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25218810

RESUMO

The most common type of liver cancer, hepatocellular carcinoma (HCC), affects over 500,000 people in the world. In the present study, liver tumor resections were used to prepare tissue arrays to examine the intensity of fluorescence of IHC stained stem cell markers in liver tissue from malignant HCC tumors and accompanying surrounding non-tumor liver. We hypothesized that a correlation exists between the fluorescence intensity of IHC stained HCC and surrounding non-tumor liver compared to liver tissue from a completely normal liver. 120 liver resection specimens (including four normal controls) were placed on a single slide to make a tissue array. They were examined by digitally quantifying the intensity of fluorescence using immuno-histochemically stained stem cell markers and protein quality control proteins. The stem cell markers were OCT3/4, Nanog, CD133, pEZH2, CD49F and SOX2. The protein quality control proteins were FAT10, UBA-6 and ubiquitin. The data collected was used to compare normal liver tissue with HCCs and parent liver tissue resected surgically using antibodies to stem cell markers and quality control protein markers. The measurements of the stem cell marker CD133 indicated an increase of fluorescence intensity for both the parent liver tissue and the HCC liver tissues. The other stem cell markers changed as follows: Nanog and OCT3/4 were decreased in both the HCCs and the parent livers; PEZH2 was reduced in the HCCs; SOX2 was increased in the parent livers compared to the controls; and CD49f was decreased in HCCs only. Protein quality control markers FAT10 and ubiquitin were downregulated in both the HCCs and the adjacent non-tumor tissue compared to the controls. UBA6 was increased in both the HCCs and the parent livers, and the levels were higher in the HCCs compared to the parent livers.


Assuntos
Carcinoma Hepatocelular/patologia , Neoplasias Hepáticas/patologia , Células-Tronco Neoplásicas/patologia , Biomarcadores Tumorais/análise , Humanos , Imuno-Histoquímica , Análise Serial de Tecidos
10.
Exp Mol Pathol ; 97(1): 81-8, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24893112

RESUMO

We previously reported the mechanisms involved in the formation of Mallory-Denk bodies (MDBs) in mice fed DDC. To further provide clinical evidence as to how ubiquitin-like protein (Ubls) modification, gene transcript expression in Ufmylation and FATylation were investigated in human archived formalin-fixed, paraffin-embedded (FFPE) liver biopsies and frozen liver sections from DDC re-fed mice were used. Real-time PCR analysis showed that all Ufmylation molecules (Ufm1, Uba5, Ufc1, Ufl1 and UfSPs) were significantly downregulated, both in DDC re-fed mice livers and patients' livers where MDBs had formed, indicating that gene transcript changes were limited to MDB-forming livers where the protein quality control system was downregulated. FAT10 and subunits of the immunoproteasome (LMP2 and LMP7) were both upregulated as previously shown. An approximate 176- and 5-fold upregulation (respectively) of FAT10 was observed in the DDC re-fed mice liver and in the livers of human alcoholic hepatitis with MDBs present, implying that there was an important role played by this gene. The FAT10-specific E1 and E2 enzymes Uba6 and USE1, however, were found to be downregulated both in patients' livers and in the liver of DDC re-fed mice. Interestedly, the downregulation of mRNA levels was proportionate to MDB abundance in the liver tissues. Our results show the first systematic demonstration of transcript regulation of Ufmylation and FATylation in the liver of patients who form MDBs, where protein quality control is downregulated. This was also shown in the livers of DDC re-fed mice where MDBs had formed.


Assuntos
Fígado Gorduroso/metabolismo , Hepatite Alcoólica/metabolismo , Cirrose Hepática Alcoólica/metabolismo , Corpos de Mallory/metabolismo , Ubiquitinas/metabolismo , Animais , Estudos de Casos e Controles , Regulação para Baixo , Fígado Gorduroso/patologia , Regulação da Expressão Gênica , Hepatite Alcoólica/patologia , Humanos , Cirrose Hepática Alcoólica/patologia , Masculino , Corpos de Mallory/efeitos dos fármacos , Corpos de Mallory/patologia , Camundongos , Camundongos Endogâmicos C3H , Hepatopatia Gordurosa não Alcoólica , Proteínas/genética , Proteínas/metabolismo , Piridinas/toxicidade , Proteínas SNARE , Enzimas Ativadoras de Ubiquitina/genética , Enzimas Ativadoras de Ubiquitina/metabolismo , Enzimas de Conjugação de Ubiquitina/genética , Enzimas de Conjugação de Ubiquitina/metabolismo , Ubiquitina-Proteína Ligases/genética , Ubiquitina-Proteína Ligases/metabolismo , Ubiquitinas/genética , Proteínas de Transporte Vesicular
11.
Exp Mol Pathol ; 96(3): 307-9, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24704429

RESUMO

Piecemeal necrosis of the liver is thought to lead to liver cell necrosis. However the process does not lead to necrosis but rather lead to gradual progressive piecemeal removal of liver cell cytoplasm by T lymphocytes which are sensitized to antigens presented on the liver cell surface to form the immunologic synapse. The cytoplasm is taken up by the T cell and digested by the lysosome in the lymphocyte. By this mechanism the liver cell gradually disappears like the Cheshire cat in Alice in Wonderland.


Assuntos
Hepatopatias/patologia , Fígado/patologia , Necrose/patologia , Citoplasma , Hepatócitos/patologia , Humanos , Fígado/citologia , Microscopia Eletrônica , Linfócitos T/patologia
12.
Eur J Clin Microbiol Infect Dis ; 33(5): 845-51, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24292099

RESUMO

Iron acquisition is a virulence factor for Staphylococcus aureus. We assessed the efficacy of the iron chelator, deferasirox (Def), alone or in combination with vancomycin (Van) against two methicillin-resistant S. aureus (MRSA) strains in vitro and in a murine bacteremia model. In vitro time-kill assays were carried out against MRSA or vancomycin-intermediate S. aureus (VISA) strains. The impact of Def on Van binding to the surface of S. aureus was measured by flow cytometry. Furthermore, we compared the efficacy of Def, Van, or both drugs in treating S. aureus bacteremia in a murine model. Combination therapy reduced MRSA and VISA viability in vitro versus either drug alone or untreated controls (p < 0.005); this outcome was correlated with enhanced Van surface binding to S. aureus cells. In vivo, Def + Van combination therapy significantly reduced the bacterial burden in mice kidneys (p = 0.005) and spleen (p < 0.001), and reduced the severity of infection with MRSA or VISA strains compared to placebo-treated mice. Our results show that Def enhances the in vitro and in vivo capacity of Van-mediated MRSA killing via a mechanism that appears to involve increased binding of Van to the staphylococcal surface. Iron chelation is a promising, novel adjunctive therapeutic strategy for MRSA and VISA infections.


Assuntos
Antibacterianos/uso terapêutico , Bacteriemia/tratamento farmacológico , Benzoatos/uso terapêutico , Quelantes/uso terapêutico , Infecções Estafilocócicas/tratamento farmacológico , Triazóis/uso terapêutico , Vancomicina/uso terapêutico , Animais , Carga Bacteriana , Deferasirox , Modelos Animais de Doenças , Quimioterapia Combinada/métodos , Ferro/metabolismo , Rim/microbiologia , Staphylococcus aureus Resistente à Meticilina/efeitos dos fármacos , Staphylococcus aureus Resistente à Meticilina/metabolismo , Camundongos Endogâmicos BALB C , Testes de Sensibilidade Microbiana , Viabilidade Microbiana/efeitos dos fármacos , Índice de Gravidade de Doença , Baço/microbiologia , Resultado do Tratamento
13.
Endocrinology ; 155(2): 417-28, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24280056

RESUMO

Nonalcoholic fatty liver disease is common in developed countries and is associated with obesity, metabolic syndrome, and type 2 diabetes. T deficiency is a risk factor for developing these metabolic deficiencies, but its role in hepatic steatosis has not been well studied. We investigated the effects of T on the pathogenesis of hepatic steatosis in rats fed a high-fat diet (HFD). Adult male rats were randomly placed into four groups and treated for 15 weeks: intact rats on regular chow diet (RCD), intact rats on liquid HFD (I+HFD), castrated rats on HFD (C+HFD), and castrated rats with T replacement on HFD (C+HFD+T). Fat contributed 71% energy to the HFD but only 16% of energy to the RCD. Serum T level was undetectable in castrated rats, and T replacement led to 2-fold higher mean serum T levels than in intact rats. C+HFD rats gained less weight but had higher percentage body fat than C+HFD+T. Severe micro- and macrovesicular fat accumulated in hepatocytes with multiple inflammatory foci in the livers of C+HFD. I+HFD and C+HFD+T hepatocytes demonstrated only mild to moderate microvesicular steatosis. T replacement attenuated HFD-induced hepatocyte apoptosis in castrated rats. Serum glucose and insulin levels were not increased with HFD in any group. Immunoblots showed that insulin-regulated proteins were not changed in any group. This study demonstrates that T deficiency may contribute to the severity of hepatic steatosis and T may play a protective role in hepatic steatosis and nonalcoholic fatty liver disease development without insulin resistance.


Assuntos
Fígado Gorduroso/tratamento farmacológico , Terapia de Reposição Hormonal , Fígado/efeitos dos fármacos , Testosterona/uso terapêutico , Adiponectina/sangue , Animais , Apoptose/efeitos dos fármacos , Composição Corporal/efeitos dos fármacos , Peso Corporal/efeitos dos fármacos , Castração , Ingestão de Alimentos/efeitos dos fármacos , Ácidos Graxos não Esterificados/sangue , Fígado Gorduroso/metabolismo , Fígado Gorduroso/patologia , Insulina/sangue , Leptina/sangue , Fígado/metabolismo , Masculino , Estresse Oxidativo/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley
14.
Exp Mol Pathol ; 95(1): 117-20, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23773849

RESUMO

Previous studies on both human and mice livers showed MDB formation in both drug hepatitis and hepatocellular carcinoma. Using the drug hepatitis mouse model of MDB formation, numerous markers for progenitor cells were found in the cells forming MDBs. In current study, using the drug hepatitis mouse model, we found that the MDB forming cells expressed two additional progenitor cell markers. These markers were CD49f and TLR4.


Assuntos
Hepatite Alcoólica/patologia , Fígado/citologia , Corpos de Mallory , Estudos de Casos e Controles , Hepatite Alcoólica/metabolismo , Humanos , Integrina alfa1/metabolismo , Fígado/patologia , Células-Tronco/metabolismo , Células-Tronco/patologia , Receptor 4 Toll-Like/metabolismo
15.
Exp Mol Pathol ; 93(3): 309-14, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22981937

RESUMO

Mallory-Denk bodies (MDBs) are aggresomes composed of undigested ubiqutinated short lived proteins which have accumulated because of a decrease in the rate of their degradation by the 26s proteasome. The decrease in the activity of the proteasome is due to a shift in the activity of the 26s proteasome to the immunoproteasome triggered by an increase in expression of the catalytic subunits of the immunoproteasome which replaces the catalytic subunits of the 26s proteasome. This switch in the type of proteasome in liver cells is triggered by the binding of IFNγ to the IFNγ sequence response element (ISRE) located on the FAT10 promoter. To determine if either FAT10 or IFNγ are essential for the formation of MDBs we fed both IFNγ and FAT10 knock out (KO) mice DDC added to the control diet for 10weeks in order to induce MDBs. Mice fed the control diet and Wild type mice fed the DDC or control diet were compared. MDBs were located by immunofluorescent double stains using antibodies to ubiquitin to stain MDBs and FAT10 to localize the increased expression of FAT10 in MDB forming hepatocytes. We found that MDB formation occurred in the IFNγ KO mice but not in the FAT10 KO mice. Western blots showed an increase in the ubiquitin smears and decreases ß 5 (chymotrypsin-like 26S proteasome subunit) in the Wild type mice fed DDC but not in the FAT10 KO mice fed DDC. To conclude, we have demonstrated that FAT10 is essential to the induction of MDB formation in the DDC fed mice.


Assuntos
Modelos Animais de Doenças , Hepatócitos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Corpos de Mallory/patologia , Ubiquitinas/fisiologia , Animais , Doença Hepática Induzida por Substâncias e Drogas/patologia , Dicarbetoxi-Di-Hidrocolidina/toxicidade , Inativação Gênica/fisiologia , Hepatócitos/metabolismo , Hepatócitos/patologia , Humanos , Interferon gama/metabolismo , Fígado/metabolismo , Fígado/patologia , Masculino , Camundongos , Camundongos Endogâmicos C3H , Camundongos Knockout , Tamanho do Órgão/efeitos dos fármacos , Complexo de Endopeptidases do Proteassoma/efeitos dos fármacos , Ligação Proteica , Elementos de Resposta/efeitos dos fármacos , Elementos de Resposta/fisiologia , Especificidade da Espécie , Ubiquitina/metabolismo
16.
Exp Mol Pathol ; 92(3): 318-26, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22465358

RESUMO

EZH2/H3K27me3 and polycomb group complex (PcG) play a major role in regulating global gene expression including tumor suppressor genes. EZH2 is linked to cell cycle regulated EZH2 phosphorylation by CDK1, a mitotic kinase which increases in arrested mitosis compared to S phase. CDK1 phosphorylation of EZH2 accelerates the degradation of pEZH2. Phospho-EZH2 is subjected to ubiquitination. The half-like of pEZH2 is shorter when compared to total EZH2. In the present study, pEZH2 was found concentrated together with ubiquitin in the Mallory-Denk bodies (MDB) that were formed in hepatocytes in the livers of drug primed mice refed DDC and humans with alcoholic hepatitis or hepatocellular carcinoma. The cells that formed MDBs in the mice livers studied were associated with a growth advantage and a high proliferative index. However, the livers from patients with alcoholic hepatitis showed evidence of cell cycle arrest where PCNA, cyclin D1 and p27 positive nuclei were numerous but Ki-67 positive nuclei were scarce. It is concluded that MDB formation is linked to the cell cycle and global gene expression (i.e. loss of gene silencing) through its association with the regulation of the polycomb group PRC2/EZH2/H3K27me3 complex.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Histonas/metabolismo , Fígado/metabolismo , Corpos de Mallory/metabolismo , Fatores de Transcrição/metabolismo , Animais , Western Blotting , Carcinoma Hepatocelular/genética , Carcinoma Hepatocelular/metabolismo , Pontos de Checagem do Ciclo Celular , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/genética , Núcleo Celular/ultraestrutura , Ciclina D1/metabolismo , Inibidor de Quinase Dependente de Ciclina p27/metabolismo , Metilação de DNA , Proteínas de Ligação a DNA/genética , Proteína Potenciadora do Homólogo 2 de Zeste , Hepatite Alcoólica/genética , Hepatite Alcoólica/metabolismo , Hepatócitos/efeitos dos fármacos , Hepatócitos/metabolismo , Hepatócitos/ultraestrutura , Humanos , Imuno-Histoquímica , Fígado/efeitos dos fármacos , Fígado/patologia , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/metabolismo , Lisina/metabolismo , Corpos de Mallory/efeitos dos fármacos , Corpos de Mallory/ultraestrutura , Metilação , Camundongos , Microscopia Eletrônica , Complexo Repressor Polycomb 2 , Antígeno Nuclear de Célula em Proliferação/metabolismo , Piridinas/toxicidade , Reação em Cadeia da Polimerase Via Transcriptase Reversa , S-Adenosilmetionina/farmacologia , Fatores de Transcrição/genética
17.
Exp Mol Pathol ; 92(2): 191-3, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22273483

RESUMO

Mallory-Denk body (MDB) formation is a component of alcoholic and non alcoholic hepatitis. Proteins of the TLR pathway were shown to be involved in the formation of MDBs, in mice fed DDC. TLR genes are upregulated and SAMe supplementation prevents this up regulation and prevented the formation of MDBs. DNA of livers from control mice, from mice fed DDC 10weeks, refed 1week with DDC and with DDC+SAMe were extracted and used to study the methylation pattern of genes involves in the TLR pathway. A PCR array was used to analyze it. Using PCR arrays for the mouse TLR pathway,24 genes were found whose expression of IL12A was regulated by the methylation of its gene. DDC fed for 10weeks reduced the methylation of the IL12A gene expression. This expression was also reduced when DDC was refed. However, when SAMe was fed, the intermediate level methylation of IL12A was up regulated to the intermediate level and the methylation of the promoter decreased compared to DDC refeeding or DDC 10weeks. IL12A is known to induce the production of IFNg by NK and L(T). We showed in a previous publication that IFNg is one of the major cytokines involved in the induction of MDB formation. The low expression of IL12A associated with the intermediate methylation of its promoter could explain one step in the mechanism which leads to the formation of MDBs.


Assuntos
Metilação de DNA , Di-Hidropiridinas/farmacologia , Subunidade p35 da Interleucina-12/genética , Fígado/efeitos dos fármacos , Fígado/metabolismo , Receptores Toll-Like/genética , Animais , Corpos de Mallory/efeitos dos fármacos , Camundongos , Regiões Promotoras Genéticas , S-Adenosilmetionina/análogos & derivados , S-Adenosilmetionina/farmacologia , Regulação para Cima/efeitos dos fármacos
18.
Exp Mol Pathol ; 91(3): 653-9, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21820428

RESUMO

Innate immunity factors such as conversion of the 26S proteasome to form the immunoproteasome and the Toll-like receptor signaling pathways are activated in chronic hepatitis induced by the carcinogenic drug DDC. Over time, preneoplastic hepatocyte phenotypes appear in the liver parenchyma. These changed hepatocytes expand in number because they have a growth advantage over normal hepatocytes when responding to chronic liver injury. The changed hepatocytes can be identified using immunofluorescent antibodies to preneoplastic cells e.g. FAT10/UbD, A2 macroglobulin, glutathione transpeptidase, alpha fetoprotein, glycipan 3, FAS, and gamma glutamyl transpeptidase. The formation of the preneoplastic cells occurs concomitant with activation of the Toll-like receptor signaling pathways and the transformation of the 26S proteasome to form the immunoproteasome. This transformation is in response to interferon stimulating response element on the promoter of the FAT10/UbD gene. NFκB, Erk, p38 and Jnk are also up regulated. Specific inhibitors block these responses in vitro in a mouse tumor cell line exposed to interferon gamma. Mallory-Denk bodies form in these preneoplastic cells, because of the depletion of the 26S proteasome due to formation of the immunoproteasome. Thus, MDB forming cells are also markers of the preneoplastic hepatocytes. The UbD positive preneoplastic cells regress when the liver injury induced chronic hepatitis subsides. When the drug DDC is refed to mice and chronic hepatitis is activated, the preneoplastic cell population expands and Mallory-Denk bodies rapidly reform. This response is remembered by the preneoplastic cells for at least four months indicating that an epigenetic cellular memory has formed in the preneoplastic cells. This proliferative response is prevented by feeding methyl donors such as S-adenosylmethionine or betaine. Drug feeding reduces the methylation of H(3) K4, 9, and 27 and this response is prevented by feeding the methyl donors. After 8 to 15months of drug withdrawal in mice the preneoplastic liver cells persist as single or small clusters of cells in the liver lobules. Multiple liver tumors form, some of which are hepatocellular carcinomas. The tumors immunostain positively for the same preneoplastic markers as the preneoplastic cells. Similar cells are identified in human cirrhosis and hepatocellular carcinoma indicating the relevance of the drug model described here to the preneoplastic changes associated with human chronic hepatitis and hepatocellular carcinoma.


Assuntos
Doença Hepática Crônica Induzida por Substâncias e Drogas/imunologia , Doença Hepática Crônica Induzida por Substâncias e Drogas/patologia , Imunidade Inata , Lesões Pré-Cancerosas/imunologia , Animais , Carcinoma Hepatocelular/etiologia , Carcinoma Hepatocelular/imunologia , Transformação Celular Neoplásica , Doença Hepática Crônica Induzida por Substâncias e Drogas/complicações , Modelos Animais de Doenças , Hepatócitos/patologia , Humanos , Neoplasias Hepáticas/etiologia , Neoplasias Hepáticas/imunologia , Camundongos , Camundongos Endogâmicos C3H
19.
Exp Mol Pathol ; 91(2): 540-7, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21708146

RESUMO

BACKGROUND: Blood alcohol levels (BAL) cycle up and down over a 7-8 day period when ethanol is fed continuously for one month in the intragastric tube feeding rat model (ITFRM) of alcoholic liver disease. The cycling phenomenon is due to an alternating increase and decrease in the metabolic rate. Recently, we found that S-adenosyl-methionine (SAMe) fed with alcohol prevented the BAL cycle. METHOD: Using the ITFRM we fed rats betaine (2 g/kg/day) with ethanol for 1 month and recorded the daily 24 h urine ethanol level (UAL) to measure the BAL cycle. UAL is equivalent to BAL because of the constant ethanol infusion. Liver histology, steatosis and BAL were measured terminally after 1 month of treatment. Microarray analysis was done on the mRNA extracted from the liver to determine the effects of betaine and alcohol on changes in gene expression. RESULTS: Betaine fed with ethanol completely prevented the BAL cycle similar to SAMe. Betaine also significantly reduced the BAL compared to ethanol fed rats without betaine. This was also observed when SAMe was fed with ethanol. The mechanism involved in both cases is that SAMe is required for the conversion of epinephrine from norepinephrine by phenylethanolamine methyltransferase (PNMT). Epinephrine is 5 to 10 fold more potent than norepinephrine in increasing the metabolic rate. The increase in the metabolic rate generates NAD, permitting ADH to increase the oxidation of alcohol. NAD is the rate limiting factor in oxidation of alcohol by alcohol dehydrogenase (ADH). This explains how SAMe and betaine prevented the cycle. Microarray analysis showed that betaine feeding prevented the up regulation of a large number of genes including TLR2/4, Il-1b, Jax3, Sirt3, Fas, Ifngr1, Tgfgr2, Tnfrsf21, Lbp and Stat 3 which could explain how betaine prevented fatty liver. CONCLUSION: Betaine feeding lowers the BAL and prevents the BAL cycle by increasing the metabolic rate. This increases the rate of ethanol elimination by generating NAD.


Assuntos
Betaína/farmacologia , Nutrição Enteral , Etanol/administração & dosagem , Etanol/sangue , Comportamento Alimentar/efeitos dos fármacos , Alanina Transaminase/sangue , Animais , Betaína/administração & dosagem , Peso Corporal/efeitos dos fármacos , Colina/sangue , Etanol/urina , Regulação da Expressão Gênica/efeitos dos fármacos , Fígado/efeitos dos fármacos , Fígado/metabolismo , Masculino , Modelos Animais , Ratos , Ratos Wistar , Sarcosina/análogos & derivados , Sarcosina/metabolismo
20.
Exp Mol Pathol ; 90(3): 252-6, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21256843

RESUMO

Recently it has been shown that the expression of the immunoproteasome increased in proportion to the degree of chronic inflammation in both the liver cell cytoplasm and nuclei in liver biopsies from patients who had chronic active hepatitis or cirrhosis. In the present study, biopsies from patients with steatohepatitis, with or without Mallory-Denk body (MDB) formation, were studied by immunofluorescent staining. Normal liver showed colocalization of FAT10, LMP2, LMP7, and MECL-1 at the mitochondria. Only LMP2 and LMP7 were found in the cell nuclei. Liver biopsies from patients with steatohepatitis and MDB formation, and a case of hepatocellular carcinoma forming MDBs in the tumor cells, showed colocalization of FAT10 and ubiquitin with LMP2, LMP7 and MECL-1 within the MDB. This indicates involvement of the immunoproteasome in MDB formation in steatohepatitis cases and in a case of HCC forming MDBs. Prior studies have shown that the immunoproteasome was involved in drug-induced MDB formation using the same immunofluorescent colocalization approach as was used on these human liver biopsies. The increase in the immunoproteasome subunit proteins was made at the expense of the 26S proteasome. This indicates that the shift from the 26S to the immunoproteasome had occurred in the MDB positive hepatocytes.


Assuntos
Carcinoma Hepatocelular/metabolismo , Fígado Gorduroso/metabolismo , Imunoproteínas/metabolismo , Neoplasias Hepáticas/metabolismo , Proteínas/metabolismo , Carcinoma Hepatocelular/patologia , Núcleo Celular/metabolismo , Cisteína Endopeptidases/metabolismo , Citoplasma/metabolismo , Fígado Gorduroso/patologia , Técnica Indireta de Fluorescência para Anticorpo , Hepatite Alcoólica/metabolismo , Hepatite Alcoólica/patologia , Humanos , Cirrose Hepática/metabolismo , Cirrose Hepática/patologia , Neoplasias Hepáticas/patologia , Mitocôndrias Hepáticas/metabolismo , Proteínas Musculares/metabolismo , Complexo de Endopeptidases do Proteassoma/metabolismo
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