Microbial Components (microbial + component)

Distribution by Scientific Domains


Selected Abstracts


Direct role of NF-,B activation in Toll-like receptor-triggered HLA-DRA expression

EUROPEAN JOURNAL OF IMMUNOLOGY, Issue 5 2006
Keun-Wook Lee
Abstract Microbial components, such as DNA containing immunostimulatory CpG motifs (CpG-DNA) and lipopolysaccharides (LPS), elicit the cell surface expression of MHC class II (MHC-II) through Toll-like receptor (TLR)/IL-1R. Here, we show that CpG-DNA and LPS induce expression of the HLA-DRA in the human B cell line, RPMI 8226. Ectopic expression of the dominant negative mutant of CIITA and RNA interference targeting the CIITA gene indicate that CIITA activation is not enough for the maximal MHC-II expression induced by CpG-DNA and LPS. Additionally, nuclear factor (NF)-,B activation is required for the CpG-DNA-activated and LPS-activated HLA-DRA expression, whereas IFN-,-induced MHC-II expression depends on CIITA rather than on NF-,B. Comprehensive mutant analyses, electrophoretic mobility shift assays and chromatin immunoprecipitation assays, reveal that the functional interaction of NF-,B with the promoter element is necessary for the TLR-mediated HLA-DRA induction by CpG-DNA and LPS. This novel mechanism provides the regulation of MHC-II gene expression with complexity and functional diversity. [source]


Requirement of phospholipase C-,2 (PLC,2) for Dectin-1-induced antigen presentation and induction of TH1/TH17 polarization

EUROPEAN JOURNAL OF IMMUNOLOGY, Issue 5 2009
Ilaria Tassi
Abstract DC recognize microbial components through an array of receptors known as PRR. PRR initiate intracellular signals, which engender DC with the capacity to stimulate T-cell responses. Dectin-1 is a PRR that recognizes ,-glucan, a major constituent of many fungi's outer cell wall. Here we show that Dectin-1 activates DC through phospholipase (PLC),2 signaling. PLC,2-deficient DC were unable to expand antigen-specific T cells and induce TH1 and TH17 differentiation in response to ,-glucan. Mechanistically, PLC,2-deficiency impaired the capacity of DC to secrete polarizing cytokines following exposure to ,-glucan. Dectin-1 required PLC,2 to activate MAPK, AP-1 and NF-,B, which induce cytokine gene expression. Moreover, PLC,2 controlled Dectin-1-mediated NFAT activation and induction of NFAT-dependent genes such as IL-2, cyclooxigenase-2 and Egr transcription factors. We conclude that PLC,2 is a crucial signaling mediator that modifies DC gene expression program to activate DC responses to ,-glucan-containing pathogens. [source]


Roles of Toll-like receptors in innate immune responses

GENES TO CELLS, Issue 9 2001
Kiyoshi Takeda
Innate immunity recognizes invading micro-organisms and triggers a host defence response. However, the molecular mechanism for innate immune recognition was unclear. Recently, a family of Toll-like receptors (TLRs) was identified, and crucial roles for these receptors in the recognition of microbial components have been elucidated. The TLR family consists of 10 members and will be expanding. Each TLR distinguishes between specific patterns of microbial components to provoke innate immune responses. The activation of innate immunity then leads to the development of antigen-specific adaptive immunity. Thus, TLRs control both innate and adaptive immune responses. [source]


Effects of glucose, cellulose, and humic acids on soil microbial eco-physiology

JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 3 2004
Oliver Dilly
Abstract Microbial eco-physiology in soils is regulated by substrate quality of the organic matter. This regulation was studied for a forest and an agricultural soil by the combination of activity and biomass techniques. Soil respiration was stimulated by the substrate quality in the order, humic acid < cellulose < glucose over 20 days. Concurrently, substrate addition increased the respiratory quotient (RQ), defined as the ratio of mol CO2 evolution per mol O2 uptake. Anabolic processes were mainly induced by glucose addition. Soil preconditioned with glucose showed a decrease in the RQ value during glucose-induced microbial growth in comparison to non-amended control. The decrease in the RQ value induced by preconditioning with cellulose and humic acid was lower. Glucose, cellulose, and humic acid addition modified the microbial biomass as estimated by fumigation-extraction (FE), substrate-induced respiration (SIR), and ATP content. Since each biomass estimate refers to specific microbial components, shifts in microbial eco-physiology and community structure induced by substrate quality were reflected by SIR : FE and SIR : ATP ratios. The active and glucose-responsive biomass in the forest soil which was earlier suggested as being dominated by K-strategists was increased in the order, humic acid < cellulose < glucose. Einfluss von Zugaben von Glucose-, Cellulose und Huminsäuren auf die mikrobielle Ökophysiologie im Boden Die Ökophysiologie der mikrobiellen Gemeinschaften in Böden ist abhängig von der Substratqualität der organischen Substanz. Dies wurde nach Zugabe von Substraten für zwei Böden, einer unter Buchenwald und einer unter Acker, anhand einer Kombination von biochemischen und physiologischen Aktivitäts- und Biomassetechniken analysiert. Die Substratzugabe erhöhte die Bodenatmung über 20 Tage hinweg in der Reihenfolge Huminsäuren < Cellulose < Glucose. Gleichzeitig wurde auch der respiratorische Quotient (RQ), definiert als das Verhältnis von CO2 -Freisetzung zu O2 -Aufnahme, durch die Substratzugabe erhöht und anabolische Prozesse induziert. Das mikrobielle Wachstum wurde in erster Linie durch Glucose stimuliert. Der mit Glucose als Substrat versetzte Boden zeigte eine Abnahme des RQ während eines glucose-induzierten Wachstums im Vergleich zur Kontrolle. Eine solche Abnahme war bei der Huminsäure- und Cellulosebehandlung geringer. Die Zugabe von Glucose, Cellulose und Huminsäuren veränderte schließlich die mikrobielle Biomasse, welche mittels Fumigation-Extraktion, substratinduzierter Atmung und ATP-Gehalt ermittelt wurde. Da jede Technik spezifische mikrobielle Komponenten erfasst, wurden Veränderungen in der mikrobiellen Ökophysiologie und der Struktur der mikrobiellen Gemeinschaften durch die Substrate induziert, die in dem SIR:FE- und SIR:ATP-Verhältnis erkennbar waren. Die aktive und glucoseaktivierbare Biomasse in einem von K-Strategen dominierten Waldboden nahm von Huminsäure-, über Cellulose- und Glucosezugabe hin zu. [source]


Hypersensitivity and oral tolerance in the absence of a secretory immune system

ALLERGY, Issue 5 2010
M. R. Karlsson
To cite this article: Karlsson M-R, Johansen F-E, Kahu H, Macpherson A, Brandtzaeg P. Hypersensitivity and oral tolerance in the absence of a secretory immune system. Allergy 2010; 65: 561,570. Abstract Background:, Mucosal immunity protects the epithelial barrier by immune exclusion of foreign antigens and by anti-inflammatory tolerance mechanisms, but there is a continuing debate about the role of secretory immunoglobulins (SIgs), particularly SIgA, in the protection against allergy and other inflammatory diseases. Lack of secretory antibodies may cause immune dysfunction and affect mucosally induced (oral) tolerance against food antigens. Methods:, We used polymeric Ig receptor (pIgR) knockout (KO) mice, which cannot export SIgA or SIgM, to study oral tolerance induction by ovalbumin (OVA) feeding and for parenteral antigen sensitization in the same animal. Results:, Remarkable systemic hyperreactivity was observed in pIgR KO mice, as 50% died after intradermal OVA challenge, which was not seen in similarly sensitized and challenged wild-type (WT) mice. Oral tolerance induced by OVA completely protected the sensitized pIgR KO mice against anaphylaxis and suppressed antibody levels (particularly IgG1) as well as delayed-type hypersensitivity (DTH) to OVA. Delayed-type hypersensitivity to a bystander antigen, human serum albumin, was also suppressed and T-cell proliferation against OVA in vitro was reduced in tolerized compared with non-tolerized pIgR KO mice. This effect was largely mediated by CD25+ T cells. Adoptive transfer of splenic putative regulatory T cells (CD4+ CD25+) obtained from OVA-fed pIgR KO mice to naïve WT mice mediated suppression of DTH against OVA after sensitization of the recipients. Conclusion:, Compensatory regulatory T-cell function becomes critical in pIgR-deficient mice to avoid the potentially catastrophic effects of systemic immune hyperreactivity, presumably resulting from defective secretory antibody-mediated immune exclusion of microbial components. [source]


Advanced molecular immunoassay system for immunobiotic lactic acid bacteria using a transfectant of Toll-like receptor 2

ANIMAL SCIENCE JOURNAL, Issue 2 2007
Masanori TOHNO
ABSTRACT Toll-like receptor 2 (TLR2) is a receptor for a variety of microbial components, and it also mediates activation signals in the cell relating to the innate immune system. In order to evaluate the precise molecular immunoregulation by various strains of lactic acid bacteria (LAB) via TLR2, the swine TLR2 (sTLR2)-expressing transfectant was constructed using human embryonic kidney (HEK) 293 cells. It is demonstrated that intact immunobiotic LAB can induce immune responses through TLR2, and that different nuclear factor-,B (NF-,B) activities of various strains can be accurately detected by sTLR2-expressing HEK293 cells. Furthermore, cellular activation of NF-,B via TLR2 is reflected in enhanced binding and uptake of LAB. The sTLR2-expressing HEK293 cells were also useful for characterizing the expression pattern of type I helper T (Th1) and type II helper T (Th2) cytokines by the stimulation of immunobiotic LAB. These results suggest that sTLR2-expressing HEK293 cells may be useful in certain molecular immunoassay systems for producing new physiologically functional foods with intestinal immunomodulatory abilities, such as the maintenance of Th1/Th2 polarization. [source]


Comparative study of the intracellular superoxide anion production in different penaeid species through the NBT-reduction assay

AQUACULTURE RESEARCH, Issue 7 2010
Cristhiane Guertler
Abstract The capacity of reactive oxygen intermediates production upon haemocyte stimulation is one of the most important immunoparameter utilized to assess the health status in cultivated shrimps. In the present study, we compared oxidative stress potential, by measuring the superoxide anion production in three penaeid shrimps: two wild Atlantic species, the pink shrimp Farfantepenaeus paulensis and the white shrimp Litopenaeus schmitti and one cultivated Pacific species, the white shrimp, Litopenaeus vannamei, through the nitro-blue-tetrazolium-reduction assay. We also proposed an optimized experimental protocol for this assay, that produces rapid and consistent results with low levels of basal superoxide anion (O2,) production by unstimulated haemocytes and high levels of this oxygen radical after cell stimulation. Among the different cell elicitors used (zymosan, laminarin, lipopolysaccharide and phorbol myristate acetate), laminarin (,-1,3-glucans , 2 mg mL,1) was the most potent cell activator for the haemocytes of all three penaeids and we recommend this immunostimulant to routinely evaluate shrimp respiratory burst. In general terms, the most elevated levels of O2, production, after cell stimulation with microbial components, were detected in L. schmitti. Interestingly, the stimulation profile of the haemocytes of L. vannamei was more similar to F. paulensis, than to L. schmitti, which is more phylogenetically related. [source]


Apoptosis signal-regulating kinase 1-mediated sustained p38 mitogen-activated protein kinase activation regulates mycoplasmal lipoprotein- and staphylococcal peptidoglycan-triggered Toll-like receptor 2 signalling pathways

CELLULAR MICROBIOLOGY, Issue 9 2005
Takeshi Into
Summary Toll-like receptor (TLR) 2 functions as a sensor for detecting various microbial components conserved in bacteria or fungi in innate immunity. TLR2 induces several signalling pathways linking to activation of the transcriptional factors NF-,B and AP-1 as well as induction of cell death. In human embryonic kidney 293 cells expressed human TLR2, mycoplasmal lipoproteins (MLP) or staphylococcal peptidoglycans (PGN) induced sustained phosphorylation of p38 mitogen-activated protein kinase (MAPK), accompanied by generation of reactive oxygen species. This observation encouraged us to examine roles of apoptosis signal-regulating kinase 1 (ASK1) in TLR2 signalling, because ASK1 is an upstream activator of p38 MAPK during exposure to oxidative stress and other stressful stimuli. A kinase-inactive mutant of ASK1 greatly impaired the sustained phosphorylation of p38 MAPK induced by MLP or PGN. This mutant also attenuated MLP- or PGN-induced transcriptional activities of NF-,B and AP-1 via inhibition of p38 MAPK activation. MLP- or PGN-induced cell death reactions, including DNA fragmentation and caspase-3/7 activation, were also downregulated by the ASK1 mutant via p38 MAPK inhibition. Furthermore, TLR2 signalling had a potential to phosphorylate and dephosphorylate ASK1 at Ser83 residue. Thus, MLP and PGN have capabilities to induce ASK1-dependent signalling pathways which regulate p38 MAPK activation through TLR2, leading to activation of NF-,B and AP-1 as well as induction of cell death. [source]