RESUMO
We studied the expression of AhR and ATG16L1 protein in experimental oxazolone-induced colitis in rats and anti-inflammatory action of recombinant antagonist of IL-1 receptors (ARIL-1) and simvastatin. The immunopositive cells were determined using an indirect immunofluorescence technique with using a monoclonal rat antibody. It has been established that development of colitis was accompanied by an increase of total number of ATG16L1-lymphocytes (by 30%, P < 0.05) in lymphoid structures of the colon. However the amount of AhR(+)-lymphocytes has not changed. At the same time has increased the concentration of ATG16L1 protein (by 4-11%, P < 0.05) in immunopositive cells. Administration of simvastatin and ARIL-1 during the development of experimental pathology was accompanied by decrease of total number of AhR(+) (by 24-38%, P < 0.05) and ATG16L1(+)-lymphocytes (by 43% - 2 fold, P < 0.05) in the colon.
Assuntos
Anti-Inflamatórios/farmacologia , Proteínas de Transporte/genética , Colite/tratamento farmacológico , Colo/metabolismo , Receptores de Hidrocarboneto Arílico/genética , Animais , Anticorpos Monoclonais/química , Proteínas Relacionadas à Autofagia , Proteínas de Transporte/imunologia , Colite/induzido quimicamente , Colite/imunologia , Colite/patologia , Colo/efeitos dos fármacos , Colo/imunologia , Colo/patologia , Regulação da Expressão Gênica , Imunofenotipagem , Contagem de Linfócitos , Linfócitos/efeitos dos fármacos , Linfócitos/imunologia , Linfócitos/patologia , Masculino , Oxazolona , Peptídeos/metabolismo , Peptídeos/farmacologia , Ratos , Ratos Wistar , Receptores de Hidrocarboneto Arílico/imunologia , Receptores de Interleucina-1/antagonistas & inibidores , Receptores de Interleucina-1/genética , Receptores de Interleucina-1/imunologia , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/farmacologia , Sinvastatina/farmacologiaRESUMO
The present study was conducted to investigate of the influence of chronic social stress and modulation of the composition of intestinal microflora on the distribution of Xbp(1+)-lymphocytes in the gut-associated lymphoid tissue of ileum of the rats. Structure of population of Xbp(1+)-cells has been studied by the analysis of serial histological sections using the method of indirect immunofluorescence with monoclonal antibodies to Xbp1 of rat. Chronic social stress development is accompanied with the reduction of total number of Xbp(1+)-lymphocytes in lymphoid structures of ileum (31% -3 fold reduction, p < 0.05), mostly expressed in lymphoidfollicles, and changes the concentration of Xbp1 protein in immunopositive cells. Modulation of the composition of intestinal microflora by antibiotics and probiotics under chronic social stress results in the increase of total number of Xbp1+ lymphocytes in gut-associated lymphoid tissue, the degree of it depends on the kind ofstress. The discovered alterations of Xbp1 expression under stress may be one of the triggers for development of autoimmune and inflammatory bowel diseases. Thus, increased understanding of the molecular actions and transcriptional networks regulated by XBP1 in immune cells may aid in the development of potential therapeutics targeting immune disorders.