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1.
Biochem Biophys Res Commun ; 276(2): 673-9, 2000 Sep 24.
Article in English | MEDLINE | ID: mdl-11027530

ABSTRACT

Intestinal epithelial cells participate in an acute phase response (APR) by responding to cytokines and by expressing acute phase protein genes. We hypothesized that butyrate, a fermentation product of the bacterial intestinal flora with deacetylase activity, affects the APR in intestinal epithelial cells. Sodium butyrate (NaBu) and Trichostatin A (TSA) induced alkaline phosphatase activity and histone H4 acetylation in IEC-6 rat intestinal epithelial cells treated with or without interleukin-1beta (IL-1). In contrast, both NaBu and TSA attenuated the IL-1-dependent induction of the acute phase protein gene haptoglobin, as well as C/EBPbeta and C/EBPdelta transcription factors mRNAs. Gel shift and supershift assays showed a strong decrease in the IL-1-induced C/EBPbeta and C/EBPdelta containing complexes binding to the HaptoA C/EBP DNA-binding site of the haptoglobin promoter, by NaBu and TSA. Furthermore, site-specific mutation of the HaptoA site abolished the NaBu- and TSA-dependent inhibition of haptoglobin, as determined by transient transfection assays. These results suggest that deacetylase inhibitors may regulate the IL-1 dependent induction of haptoglobin by down-regulating C/EBP isoforms, and that C/EBPs represent a target for the action of butyrate in the control of the APR of intestinal epithelial cells.


Subject(s)
Butyrates/pharmacology , CCAAT-Enhancer-Binding Proteins/physiology , Haptoglobins/biosynthesis , Histone Deacetylase Inhibitors , Interleukin-1/physiology , Intestinal Mucosa/metabolism , Animals , CCAAT-Enhancer-Binding Protein-beta/genetics , CCAAT-Enhancer-Binding Protein-beta/metabolism , Cells, Cultured , Enzyme Inhibitors/pharmacology , Epithelial Cells/metabolism , Gene Expression/drug effects , Haptoglobins/genetics , Intestines/cytology , Intestines/drug effects , Protein Isoforms/physiology , RNA, Messenger/biosynthesis , RNA, Messenger/drug effects , Rats
2.
Biochem Biophys Res Commun ; 259(3): 544-9, 1999 Jun 16.
Article in English | MEDLINE | ID: mdl-10364455

ABSTRACT

In addition to important roles in the regulation of cell growth and cell restitution, both pro- and anti-inflammatory effects have been ascribed to TGFbeta in intestinal epithelial cells. However, the mechanisms involved in TGFbeta-dependent anti-inflammatory activities remain to be determined. In the rat intestinal epithelial cell line IEC-6, TGFbeta attenuated the glucocorticoid-dependent increases in mRNA levels of the acute phase protein gene haptoglobin, and of C/EBP isoforms beta and delta. Supershift assays demonstrated a TGFbeta-mediated decrease in the binding of C/EBP isoforms beta and delta to the haptoA and haptoC C/EBP DNA-binding sites from the haptoglobin promoter. Mutations of both HaptoA and HaptoC sites abolished the glucocorticoid-dependent activation and the TGFbeta-mediated attenuation of the haptoglobin promoter, as assessed by transient transfection assays. TGFbeta induced p42/p44 MAP kinase activities. Treatment with the MEK 1/2 inhibitor PD 98059 abolished TGFbeta attenuation. These results suggest that C/EBP isoforms are involved both in the glucocorticoid-dependent induction and in the TGFbeta-mediated attenuation of haptoglobin expression. Furthermore, p42/p44 MAP kinases may function in a TGFbeta-dependent signaling pathway leading to attenuation of haptoglobin expression.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Gene Expression Regulation , Haptoglobins/genetics , Transforming Growth Factor beta/pharmacology , Animals , Cell Line , DNA-Binding Proteins/metabolism , Dexamethasone/pharmacology , Down-Regulation , Enzyme Inhibitors/pharmacology , Epithelial Cells , Flavonoids/pharmacology , Glucocorticoids/pharmacology , Haptoglobins/metabolism , RNA, Messenger/analysis , Rats , Signal Transduction , Time Factors , Transfection
6.
Can Vet J ; 23(6): 179-82, 1982 Jun.
Article in English | MEDLINE | ID: mdl-17422149

ABSTRACT

EPIZOOTIOLOGICAL ASPECTS OF PORCINE RESPIRATORY DISEASES WHICH WERE ENCOUNTERED IN QUEBEC FROM SEPTEMBER 1980 UNTIL FEBRUARY 1981: In the spring of 1981, a questionnaire was mailed to pig farmers of Quebec, in order to determine the epizootiological factors susceptible to account for the deaths which had occurred during the period extending from September 1980 until February 1981. The mortality rate was estimated at 4.5% for that period. It proved to be higher on the farms where hogs were fattened only (5.9%), compared to those where they were raised and fattened (3.4%) and for those where the hogs were owned (6.8%) compared to those where they were fattened by contract (4.3%). During that six month period, severe mortality problems (>/= 4%) were experienced by approximately 32% of the hog producers in Quebec, mainly by those who were fattening hogs. The mortality rate was found to be proportional to the size of the herds; it proved to be definitely higher when the pigs had been bought at auction sales or from livestock dealers and even higher when the pigs had been simultaneously obtained from both sources. The results of this investigation and the importance of some epizootiological factors are discussed. The economical loss for the Province was estimated at $15 120 000 for the 126 000 pigs which died during that six month period.

7.
Can Vet J ; 21(10): 278-9, 1980 Oct.
Article in English | MEDLINE | ID: mdl-7438003

ABSTRACT

The prevalence of reactors to different serovars of Leptospira interrogans was determined in 117 swine premises in Quebec. A total of 926 sera were tested, using the microscopic agglutination method, against six leptospiral serovars: pomona, icterohaemorrhagiae, grippotyphosa, hardjo, canicola and ballum. Of the sera tested, 30 (3.2%) reacted to one of the three following serovars: pomona (2%), icterohaemorrhagiae (1.1%) and ballum (0.1%).


Subject(s)
Antibodies, Bacterial/analysis , Leptospirosis/veterinary , Swine Diseases/immunology , Animals , Leptospira interrogans/immunology , Leptospirosis/immunology , Swine
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