Literature DB >> 6403355

The distribution, ontogeny and origin in the rat of Ia-positive cells with dendritic morphology and of Ia antigen in epithelia, with special reference to the intestine.

G Mayrhofer, C W Pugh, A N Barclay.   

Abstract

Ia antigens were localized in cryostat sections of rat intestine and other tissues by an indirect immunoperoxidase technique using monoclonal antibodies that recognize the rat antigens homologous to the gene products of the I-A and I-E subregions of the mouse major histocompatibility complex (MHC). Two categories of Ia+ cells were characterized, namely epithelial cells and bone marrow-derived cells with dendritic morphology. In the small intestine Ia antigen was present in the distal 2/3 of the absorptive epithelium but absent from the bases of the villi, the crypts and the epithelium covering the Peyer's patches. The distribution in nude rats was similar, indicating that T lymphocytes are not obligatory for its expression. In ontogeny Ia antigen was absent in the epithelium of neonatal gut, appearing at about 4 weeks of age and reaching adult levels at about 6 weeks. Different rat strains showed large differences in the amount of Ia antigen expressed by villus epithelium and the traits for the level of expression were shown to map outside the MHC. The levels of expression of Ia antigen in the proximal tubules of the kidney followed that of the gut epithelium in the different strains and in both tissues was mostly intracellular. Studies with chimeras showed that the Ia antigen in epithelial cells was not acquired from bone marrow-derived cells. The second category of cell studied had a characteristic dendritic morphology and was present in large numbers in the lamina propria of the villi and in the crypts. In the Peyer's patches these cells were present both in the subepithelial dome region and within the epithelium itself. These Ia+ dendritic cells were present in nude rat jejunum and appeared in normal fetal gut by 18 days gestation and were also shown to migrate into antigen-free grafts of fetal gut. This suggests that they do not require stimulation from antigens, bacterial products or T lymphocytes in order to localize in the gut or to express Ia antigen. Studies with other cell surface markers suggest that the Ia+ cells with dendritic morphology represent a range of cell types, some with similarities to macrophages and others to nonphagocytic dendritic cells.

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Year:  1983        PMID: 6403355     DOI: 10.1002/eji.1830130206

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  76 in total

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2.  Ontogeny of macrophage subpopulations and Ia-positive dendritic cells in pulmonary tissue of the rat.

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3.  Difference between bacterial and food antigens in mucosal immunogenicity.

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4.  Macrophages in the interstitial tissue of the rat testis.

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5.  Network of dendritic cells within the muscular layer of the mouse intestine.

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6.  The larynx as an immunological organ: immunological architecture in the pig as a large animal model.

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7.  Murine gut epithelial cells express Ia molecules antigenically distinct from those of conventional antigen-presenting cells.

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Journal:  Immunol Res       Date:  1991       Impact factor: 2.829

8.  Class II MHC antigens in the rat digestive system. Normal distribution and induced expression after interferon-gamma treatment in vivo.

Authors:  B Steiniger; P Falk; M Lohmüller; P H van der Meide
Journal:  Immunology       Date:  1989-12       Impact factor: 7.397

9.  Local cellular immune response in ascending urinary tract infection: occurrence of T-cells, immunoglobulin-producing cells, and Ia-expressing cells in rat urinary tract tissue.

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Journal:  Infect Immun       Date:  1984-06       Impact factor: 3.441

10.  Epithelial cells in fetal intestine produce chemerin to recruit macrophages.

Authors:  Akhil Maheshwari; Ashish R Kurundkar; Sadiq S Shaik; David R Kelly; Yolanda Hartman; Wei Zhang; Reed Dimmitt; Shehzad Saeed; David A Randolph; Charles Aprahamian; Geeta Datta; Robin K Ohls
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-05-14       Impact factor: 4.052

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