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1.
Cell Microbiol ; 8(3): 485-95, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16469059

RESUMO

Lactobacillus gasseri OLL2716 has recently been discovered as a probiotic that suppresses the growth of Helicobacter pylori and reduces gastric mucosal inflammation in humans. This has resulted in the development of a new type of probiotic yoghurt 'LG21' in Japan. In our previous study, we found an immunostimulatory AT5ACL oligodeoxynucleotide (AT-ODN) containing a unique core sequence (5'-ATTTTTAC-3') in L. gasseri JCM1131(T). Interestingly, although the AT-ODN does not contain any CpG sequences, it exerts mitogenic activity in B cells and augments Th-1-type immune responses via Toll-like receptor 9. These findings prompted us to identify strong immunostimulatory non-CpG AT-ODNs that contain the 5'-ATTTTTAC-3' motif in the genomic sequence of L. gasseri OLL2716. We identified 280 kinds of AT-ODNs in the L. gasseri OLL2716 genome. Mitogenicity and NF-kappaB gene reporting assays showed that 13 of the 280 AT-ODNs were strongly immunostimulatory when in the TLR9 transfectant. Of these, AT-ODNs LGAT-145 and LGAT-243 were the most potent. With respect to the induction of Th-1-type cytokines, LGAT-243 had the greatest activity and was more potent than the swine prototype, ODN D25. We further found that a six-base secondary loop structure containing a self-stabilized 5'-C...G-3' stem sequence is important for potent immunostimulatory activity. These results show for the first time that AT-ODNs with a specific loop and stem structure are important factors for immunostimulatory activity. Finally, we found that novel strong immunostimulatory non-CpG AT-ODNs exist in the genome of probiotic lactic acid bacteria.


Assuntos
Sequência Rica em At/imunologia , Lactobacillus/imunologia , Oligodesoxirribonucleotídeos/química , Oligodesoxirribonucleotídeos/imunologia , Probióticos , Animais , Sequência de Bases , Células CHO , Cricetinae , Humanos , Intestinos/citologia , Intestinos/imunologia , Lactobacillus/química , Leucócitos Mononucleares/imunologia , Dados de Sequência Molecular , Nódulos Linfáticos Agregados/citologia , Nódulos Linfáticos Agregados/imunologia , Suínos , Receptor Toll-Like 9/genética , Transfecção
2.
Biochem Biophys Res Commun ; 326(4): 782-7, 2005 Jan 28.
Artigo em Inglês | MEDLINE | ID: mdl-15607737

RESUMO

Toll-like receptor 9, which is expressed on the surface of antigen presenting cells and which was recently identified in the cytoplasmic follicle, recognizes bacterial CpG oligodeoxynucleotides (ODNs), resulting in the induction of a potent immune response. However, in our previous study, we found that TLR9 potentially recognizes not only CpG ODN but also non-CpG ODN such as AT ODN. Therefore, in the present study, to investigate this possibility, we elucidated the effects of AT ODN on T(H)-1, T(H)-2 type cytokine induction via TLR9 by real-time quantitative PCR analysis and ELISA of the swine TLR9 transfectant. The results demonstrated that the T(H)-1 type cytokines such as interleukin (IL)-12p70 and interferon (IFN)-gamma were strongly induced by AT ODN compared to the unexposed controls, while T(H)-2 type cytokines were not induced. These results indicate that the AT ODN can augment the T(H)-1 immune response, which plays an important role in prevention of allergic responses. Moreover, the swine TLR9 transfectant demonstrated its usefulness for evaluation of immunostimulation by bacterial DNA through the detection of T(H)-1, T(H)-2 type cytokine induction via TLR9 signaling.


Assuntos
Sequência Rica em At/imunologia , DNA Bacteriano/administração & dosagem , Rim/imunologia , Lactobacillus/genética , Glicoproteínas de Membrana/imunologia , Oligodesoxirribonucleotídeos/farmacologia , Receptores de Superfície Celular/imunologia , Transdução de Sinais/fisiologia , Animais , Linhagem Celular , Ilhas de CpG/imunologia , Relação Dose-Resposta a Droga , Humanos , Rim/efeitos dos fármacos , Rim/embriologia , Oligodesoxirribonucleotídeos/imunologia , Transdução de Sinais/efeitos dos fármacos , Suínos , Células Th1/efeitos dos fármacos , Células Th1/imunologia , Receptor Toll-Like 9 , Receptores Toll-Like
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