Literature DB >> 21509613

Changes in lamina propria dendritic cells on the oral administration of exogenous protein antigens during weaning.

Ryuji Ohue1, Masahiro Nakamoto, Naofumi Kitabatake, Fumito Tani.   

Abstract

Two critical periods of maximum exposure to antigens occur in young mammals, immediately after birth and at weaning, as a result of colonization by commensal bacteria and the ingestion of new diets. At weaning, active immune responses of antibody production against dietary proteins are known to occur, but simultaneously, oral tolerance is acquired for harmless food proteins. However, regulated mechanisms of the immune system at weaning remain to be elucidated although its immune responses may be somewhat similar to those in adulthood. Considering that tolerogenic antigen-presenting cells (APCs) are likely to be a key factor in the acquisition of oral tolerance, in the present study, we examined the changes of dendritic cells (DCs) in the lamina propria (LP) on exposure to food proteins at weaning. C57BL/6 female mice were weaned at the age of 3 weeks and orally administered 10 mg of ovalbumin (OVA) for ten consecutive days after weaning. The administration led to a decrease in the plasma level of immunoglobulin specific for OVA, suggesting the acquisition of oral tolerance. The uptake of fluorescence-labeled OVA was significantly observed for CD11c(+)LPDCs. When we analyzed the changes of two types of LPDCs, PDCA-1(+) MHC II(+) DCs and CD103(+) MHC II(+) DCs, ten consecutive gavages of OVA marginally, but not significantly, augmented only the frequency of PDCA-1(+) MHC II(+) DCs. Considering that the change of APCs likely appears immediately on the response to antigen intake, we found the statistically significant increase in the frequency of PDCA-1(+) DCs, but not in that of CD103(+) DCs, even after two treatments, indicating PDCA-1(+) DCs to be recruited in the LP within 2 days of exposure to food proteins. These results suggest that the behavior of tolerogenic PDCA-1(+) DCs may change at weaning with the removal of the immunoprotective components of maternal milk.

Entities:  

Year:  2011        PMID: 21509613      PMCID: PMC3386394          DOI: 10.1007/s10616-011-9351-z

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  41 in total

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Journal:  Eur J Immunol       Date:  2001-04       Impact factor: 5.532

Review 2.  Anatomical basis of tolerance and immunity to intestinal antigens.

Authors:  Allan McI Mowat
Journal:  Nat Rev Immunol       Date:  2003-04       Impact factor: 53.106

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Journal:  Nat Immunol       Date:  2001-04       Impact factor: 25.606

Review 4.  Involvement of intestinal dendritic cells in oral tolerance, immunity to pathogens, and inflammatory bowel disease.

Authors:  Brian L Kelsall; Francisco Leon
Journal:  Immunol Rev       Date:  2005-08       Impact factor: 12.988

Review 5.  Subsets of migrating intestinal dendritic cells.

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Journal:  Immunol Rev       Date:  2010-03       Impact factor: 12.988

Review 6.  Tuning microenvironments: induction of regulatory T cells by dendritic cells.

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Journal:  Immunity       Date:  2008-09-19       Impact factor: 31.745

7.  Expanding dendritic cells in vivo enhances the induction of oral tolerance.

Authors:  J L Viney; A M Mowat; J M O'Malley; E Williamson; N A Fanger
Journal:  J Immunol       Date:  1998-06-15       Impact factor: 5.422

8.  Oral tolerance originates in the intestinal immune system and relies on antigen carriage by dendritic cells.

Authors:  Tim Worbs; Ulrike Bode; Sheng Yan; Matthias W Hoffmann; Gabriele Hintzen; Günter Bernhardt; Reinhold Förster; Oliver Pabst
Journal:  J Exp Med       Date:  2006-03-13       Impact factor: 14.307

9.  Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid.

Authors:  Cheng-Ming Sun; Jason A Hall; Rebecca B Blank; Nicolas Bouladoux; Mohamed Oukka; J Rodrigo Mora; Yasmine Belkaid
Journal:  J Exp Med       Date:  2007-07-09       Impact factor: 14.307

10.  Small intestinal CD103+ dendritic cells display unique functional properties that are conserved between mice and humans.

Authors:  Elin Jaensson; Heli Uronen-Hansson; Oliver Pabst; Bertus Eksteen; Jiong Tian; Janine L Coombes; Pia-Lena Berg; Thomas Davidsson; Fiona Powrie; Bengt Johansson-Lindbom; William W Agace
Journal:  J Exp Med       Date:  2008-08-18       Impact factor: 14.307

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  1 in total

Review 1.  Vitamin A and immune regulation: role of retinoic acid in gut-associated dendritic cell education, immune protection and tolerance.

Authors:  Barbara Cassani; Eduardo J Villablanca; Jaime De Calisto; Sen Wang; J Rodrigo Mora
Journal:  Mol Aspects Med       Date:  2011-11-22
  1 in total

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