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10.1016/j.ajpath.2015.12.015

http://scihub22266oqcxt.onion/10.1016/j.ajpath.2015.12.015
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C4861757!4861757!26948422
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suck abstract from ncbi


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pmid26948422      Am+J+Pathol 2016 ; 186 (5): 1166-79
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  • Induction of Colonic M Cells during Intestinal Inflammation #MMPMID26948422
  • Bennett KM; Parnell EA; Sanscartier C; Parks S; Chen G; Nair MG; Lo DD
  • Am J Pathol 2016[May]; 186 (5): 1166-79 PMID26948422show ga
  • Intestinal M (microfold) cells are specialized epithelial cells overlying lymphoid tissues in the small intestine. Unlike common enterocytes, M cells lack an organized apical brush border, and are able to transcytose microparticles across the mucosal barrier to underlying antigen-presenting cells. We found that in both the dextran sodium sulfate and Citrobacter rodentium models of colitis, significantly increased numbers of Peyer's patch (PP) phenotype M cells were induced at the peak of inflammation in colonic epithelium, often accompanied by loosely organized lamina propria infiltrates. PP type M cells are thought to be dependent on cytokines, including tumor necrosis factor (TNF)-? and receptor activator of nuclear factor kappa-B ligand; these cytokines were also found to be induced in the inflamed tissues. The induction of M cells was abrogated by anti?TNF-? blockade, suggesting that anti?TNF-? therapies may have similar effects in clinical settings, although the functional consequences are not clear. Our results suggest that inflammatory cytokine-induced PP type M cells may be a useful correlate of chronic intestinal inflammation.
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