scholarly journals Differentiation of Epithelial cells to M Cells in Response to Bacterial Colonization on the Follicle-Associated Epithelium of Peyer's Patch in Rat Small Intestine

2006 ◽  
Vol 68 (10) ◽  
pp. 1023-1028 ◽  
Author(s):  
Keigi CHIN ◽  
Sachiko ONISHI ◽  
Midori YUJI ◽  
Tetsurou INAMOTO ◽  
Wang-Mei QI ◽  
...  
2007 ◽  
Vol 69 (5) ◽  
pp. 501-508 ◽  
Author(s):  
Sachiko ONISHI ◽  
Toshifumi YOKOYAMA ◽  
Keigi CHIN ◽  
Midori YUJI ◽  
Tetsurou INAMOTO ◽  
...  

1987 ◽  
Vol 247 (3) ◽  
pp. 537-546 ◽  
Author(s):  
MarianR. Neutra ◽  
TeresaL. Phillips ◽  
EllenL. Mayer ◽  
DouglasJ. Fishkind

2008 ◽  
Vol 180 (12) ◽  
pp. 7840-7846 ◽  
Author(s):  
Kazutaka Terahara ◽  
Masato Yoshida ◽  
Osamu Igarashi ◽  
Tomonori Nochi ◽  
Gemilson Soares Pontes ◽  
...  

2004 ◽  
Vol 200 (2) ◽  
pp. 235-245 ◽  
Author(s):  
Marina N. Fleeton ◽  
Nikhat Contractor ◽  
Francisco Leon ◽  
J. Denise Wetzel ◽  
Terence S. Dermody ◽  
...  

We explored the role of Peyer's patch (PP) dendritic cell (DC) populations in the induction of immune responses to reovirus strain type 1 Lang (T1L). Immunofluorescence staining revealed the presence of T1L structural (σ1) and nonstructural (σNS) proteins in PPs of T1L-infected mice. Cells in the follicle-associated epithelium contained both σ1 and σNS, indicating productive viral replication. In contrast, σ1, but not σNS, was detected in the subepithelial dome (SED) in association with CD11c+/CD8α−/CD11blo DCs, suggesting antigen uptake by these DCs in the absence of infection. Consistent with this possibility, PP DCs purified from infected mice contained σ1, but not σNS, and PP DCs from uninfected mice could not be productively infected in vitro. Furthermore, σ1 protein in the SED was associated with fragmented DNA by terminal deoxy-UTP nick-end labeling staining, activated caspase-3, and the epithelial cell protein cytokeratin, suggesting that DCs capture T1L antigen from infected apoptotic epithelial cells. Finally, PP DCs from infected mice activated T1L-primed CD4+ T cells in vitro. These studies show that CD8α−/CD11blo DCs in the PP SED process T1L antigen from infected apoptotic epithelial cells for presentation to CD4+ T cells, and therefore demonstrate the cross-presentation of virally infected cells by DCs in vivo during a natural viral infection.


1995 ◽  
Vol 279 (2) ◽  
pp. 433-436 ◽  
Author(s):  
Thomas H. Ermak ◽  
Edward P. Dougherty ◽  
Hitesh R. Bhagat ◽  
Zita Kabok ◽  
Jacques Pappo

Virology ◽  
2021 ◽  
Vol 552 ◽  
pp. 43-51
Author(s):  
Ya-Mei Chen ◽  
Emma T. Helm ◽  
Jennifer M. Groeltz-Thrush ◽  
Nicholas K. Gabler ◽  
Eric R. Burrough

1992 ◽  
Vol 29 (2) ◽  
pp. 120-128 ◽  
Author(s):  
M. Paar ◽  
E. M. Liebler ◽  
J. F. Pohlenz

Uptake of macromolecules (e.g., ferritin) by M cells in follicle-associated epithelium in small and large intestine was investigated in three healthy, conventionally raised, 2- to 3-week-old, female Holstein Frisian calves. A 2.5% solution of ferritin was injected into the ligated loops in mid-jejunum, in terminal ileum, in the ascending colon adjacent to the ileocecal junction, and in the proximal loop of the ascending colon containing gut-associated lymphoid tissue. After exposure times that ranged from 82 to 165 minutes, ferritin was detected in M cells of domes in the small intestine, as well as in cells in follicle-associated epithelium of proprial lymphoid nodules and lymphoglandular complexes of colon that morphologically resembled M cells of small intestine. Ferritin was found in apical invaginations, apical vesicles, multivesicular bodies, basal vesicles, and adjacent intercellular spaces. In addition to ferritin, apical vesicles, multivesicular bodies, and intercellular spaces contained 50-nm membrane-bound particles. More ferritin was endocytosed by M cells of the small intestine than by M cells of the large intestine. In the large intestine, higher amounts of ferritin were found in M cells of follicle-associated epithelium overlying proprial lymphoid nodules than in M cells of follicle-associated epithelium in the depth of lymphoglandular complexes. Based on these results, we concluded that M cells of follicle-associated epithelium in the colon of calves provide a route for antigen uptake into the intestinal lymphoid system.


2010 ◽  
Vol 78 (8) ◽  
pp. 3570-3577 ◽  
Author(s):  
Luiz E. Bermudez ◽  
Mary Petrofsky ◽  
Sandra Sommer ◽  
Raúl G. Barletta

ABSTRACT Mycobacterium avium subsp. paratuberculosis, the agent of Johne's disease, infects ruminant hosts by translocation through the intestinal mucosa. A number of studies have suggested that M. avium subsp. paratuberculosis interacts with M cells in the Peyer's patches of the small intestine. The invasion of the intestinal mucosa by M. avium subsp. paratuberculosis and Mycobacterium avium subsp. hominissuis, a pathogen known to interact with intestinal cells, was compared. M. avium subsp. paratuberculosis was capable of invading the mucosa, but it was significantly less efficient at dissemination than M. avium subsp. hominissuis. B-cell knockout (KO) mice, which lack Peyer's patches, were used to demonstrate that M. avium subsp. paratuberculosis enters the intestinal mucosa through enterocytes in the absence of M cells. In addition, the results indicated that M. avium subsp. paratuberculosis had equal abilities to cross the mucosa in both Peyer's patch and non-Peyer's patch segments of normal mice. M. avium subsp. paratuberculosis was also shown to interact with epithelial cells by an α5β1 integrin-independent pathway. Upon translocation, dendritic cells ingest M. avium subsp. paratuberculosis, but this process does not lead to efficient dissemination of the infection. In summary, M. avium subsp. paratuberculosis interacts with the intestinal mucosa by crossing both Peyer's patches and non-Peyer's patch areas but does not translocate or disseminate efficiently.


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