2017
DOI: 10.1292/jvms.17-0470
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Mechanism of M-cell differentiation accelerated by proliferation of indigenous bacteria in rat Peyer’s patches

Abstract: The mechanism by which indigenous bacteria on the follicle-associated epithelium (FAE) of lymphatic follicles (LFs) accelerate the differentiation of microvillous columnar epithelial cells (MV) into M-cells was immunohistochemically investigated in rat Peyer’s patches. The results showed that the number of Toll-like receptor (TLR) -4+ M-cells was greater in the FAE with expansion of bacterial colonies (LFs with bacterial colonies on the FAE: b-LF) than the FAE without expansion of bacterial colonies (nb-LF). T… Show more

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Cited by 4 publications
(2 citation statements)
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“…It was shown that in mice specific bacteria determine mucosal IgA production with followed mucosal immune response, they enhance intestinal IgA levels by inducing TGF-β in T follicular helper cells of PP Bacteria belonged to Anaeroplasma are sufficient to induce these changes [9]. In rat's PP the indigenous bacteria accelerate the differentiation of microvillous columnar epithelial cells into M-cells [10]. The growth of bacterial colonies between the intervillous spaces associates with the change of histological localization of the lymphocyte lineage in small intestine mucosa of rats [11].…”
Section: Discussionmentioning
confidence: 99%
“…It was shown that in mice specific bacteria determine mucosal IgA production with followed mucosal immune response, they enhance intestinal IgA levels by inducing TGF-β in T follicular helper cells of PP Bacteria belonged to Anaeroplasma are sufficient to induce these changes [9]. In rat's PP the indigenous bacteria accelerate the differentiation of microvillous columnar epithelial cells into M-cells [10]. The growth of bacterial colonies between the intervillous spaces associates with the change of histological localization of the lymphocyte lineage in small intestine mucosa of rats [11].…”
Section: Discussionmentioning
confidence: 99%
“…After euthanasia by overdose peritoneal injection of pentobarbital sodium (Kyoritsu Seiyaku Corp., Tokyo, Japan), tissue blocks were removed from the ileum including the Peyer’s patches. Then, the tissue blocks were immersion-fixed in 4.0% paraformaldehyde fixative in 0.1 M phosphate buffer for 6 hr at 4°C, and snap-frozen in liquid nitrogen as described in a previous study [47]. Four micrometer-thick sections were cut using a Coldtome Leica CM1950 (Leica Biosystems, Nussloch, Germany), placed on slide glasses precoated with 0.2% 3-aminopropyltriethoxysilane (Shin-Etsu Chemical Co., Tokyo, Japan), and stored at −30°C until use.…”
Section: Methodsmentioning
confidence: 99%