Literature DB >> 27921148

Metabolites: deciphering the molecular language between DCs and their environment.

Lucía Minarrieta1, Peyman Ghorbani1, Tim Sparwasser1, Luciana Berod2.   

Abstract

Dendritic cells (DCs) determine the outcome of the immune response based on signals they receive from the environment. Presentation of antigen under various contexts can lead to activation and differentiation of T cells for immunity or dampening of immune responses by establishing tolerance, primarily through the priming of regulatory T cells. Infections, inflammation and normal cellular interactions shape DC responses through direct contact or via cytokine signaling. Although it is widely accepted that DCs sense microbial components through pattern recognition receptors (PRRs), increasing evidence advocates for the existence of a set of signals that can profoundly shape DC function via PRR-independent pathways. This diverse group of host- or commensal-derived metabolites represents a newly appreciated code from which DCs can interpret environmental cues. In this review, we discuss the existing information on the effect of some of the most studied metabolites on DC function, together with the implications this may have in immune-mediated diseases.

Entities:  

Keywords:  Dendritic cells; Metabolism; Metabolites; Microbiota; Tolerance; Vitamins

Mesh:

Substances:

Year:  2016        PMID: 27921148     DOI: 10.1007/s00281-016-0609-6

Source DB:  PubMed          Journal:  Semin Immunopathol        ISSN: 1863-2297            Impact factor:   9.623


  272 in total

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2.  DCs metabolize sunlight-induced vitamin D3 to 'program' T cell attraction to the epidermal chemokine CCL27.

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Journal:  Nat Immunol       Date:  2007-01-28       Impact factor: 25.606

3.  Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells.

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Journal:  Nature       Date:  2013-11-13       Impact factor: 49.962

4.  Inhibition of HDAC9 increases T regulatory cell function and prevents colitis in mice.

Authors:  Edwin F de Zoeten; Liqing Wang; Hong Sai; Wolfgang H Dillmann; Wayne W Hancock
Journal:  Gastroenterology       Date:  2009-10-29       Impact factor: 22.682

5.  Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43.

Authors:  Kendle M Maslowski; Angelica T Vieira; Aylwin Ng; Jan Kranich; Frederic Sierro; Di Yu; Heidi C Schilter; Michael S Rolph; Fabienne Mackay; David Artis; Ramnik J Xavier; Mauro M Teixeira; Charles R Mackay
Journal:  Nature       Date:  2009-10-29       Impact factor: 49.962

6.  The A2B adenosine receptor impairs the maturation and immunogenicity of dendritic cells.

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Journal:  J Immunol       Date:  2009-04-15       Impact factor: 5.422

7.  Induction of Treg by monocyte-derived DC modulated by vitamin D3 or dexamethasone: differential role for PD-L1.

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9.  The multidrug resistance (mdr1) gene product functions as an ATP channel.

Authors:  E H Abraham; A G Prat; L Gerweck; T Seneveratne; R J Arceci; R Kramer; G Guidotti; H F Cantiello
Journal:  Proc Natl Acad Sci U S A       Date:  1993-01-01       Impact factor: 11.205

10.  Commensal-pathogen interactions in the intestinal tract: lactobacilli promote infection with, and are promoted by, helminth parasites.

Authors:  Lisa A Reynolds; Katherine A Smith; Kara J Filbey; Yvonne Harcus; James P Hewitson; Stephen A Redpath; Yanet Valdez; María J Yebra; B Brett Finlay; Rick M Maizels
Journal:  Gut Microbes       Date:  2014-08-05
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Authors:  Francisco J Quintana
Journal:  Semin Immunopathol       Date:  2017-01-16       Impact factor: 9.623

3.  Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication.

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4.  Butyrate Conditions Human Dendritic Cells to Prime Type 1 Regulatory T Cells via both Histone Deacetylase Inhibition and G Protein-Coupled Receptor 109A Signaling.

Authors:  Maria M M Kaisar; Leonard R Pelgrom; Alwin J van der Ham; Maria Yazdanbakhsh; Bart Everts
Journal:  Front Immunol       Date:  2017-10-30       Impact factor: 7.561

Review 5.  Intestinal microbiota: a new force in cancer immunotherapy.

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Review 6.  Gut Microbiota and Immunotherapy.

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  6 in total

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