scholarly journals Role of acetylcholine on the isotype switching in Peyer's patches and lamina propria for IgA secretion in small intestine of BALB/c mice.

2015 ◽  
Vol 6 ◽  
Author(s):  
Salas Pimentel Marisol ◽  
Reséndiz Albor Aldo ◽  
Arciniega Martínez Ivonne ◽  
Martínez Becerril Elia ◽  
García Fonseca Alan ◽  
...  
Blood ◽  
2000 ◽  
Vol 96 (4) ◽  
pp. 1538-1544
Author(s):  
Anil Mishra ◽  
Simon P. Hogan ◽  
Eric B. Brandt ◽  
Marc E. Rothenberg

The gastrointestinal immune system is traditionally thought to be composed of lymphocytes located within Peyer's patches and the lamina propria. We have recently reported that eosinophils also reside in the gastrointestinal tract during healthy states, in particular, within the lamina propria, and that these cells substantially increase after oral allergen exposure. We now demonstrate the presence of eosinophils in Peyer's patches and characterize the signals that regulate the accumulation of eosinophils in Peyer's patches. In contrast to the lamina propria, intestinal Peyer's patches have very low levels of eosinophils under healthy states. However, elevated levels of interleukin-5 (IL-5), generated by transgenic or pharmacologic approaches, result in a dramatic increase in eosinophil levels in Peyer's patches. Most eosinophils are located in the outer cortex and interfollicular regions of the Peyer's patches. To dissect the mechanism of eosinophil trafficking to Peyer's patches, the role of eotaxin was examined. Mice transgenic for IL-5 and genetically deficient in eotaxin were found to have reduced levels of eosinophils in Peyer's patches compared with IL-5-transgenic mice. To prove that eosinophils also traffic to Peyer's patches in wild-type mice, allergic hypersensitivity was induced and Peyer's patches were examined. Exposure to mucosal allergen promoted marked accumulation of eosinophils in Peyer's patches and this process was attenuated in eotaxin-deficient mice. In summary, these data demonstrate that elevated levels of IL-5 and mucosal allergen exposure promote eotaxin-dependent eosinophil trafficking to Peyer's patches. These studies suggest that eosinophils may cooperate with lymphocytes in the development of mucosal immune responses in the gastrointestinal tract.


Blood ◽  
2000 ◽  
Vol 96 (4) ◽  
pp. 1538-1544 ◽  
Author(s):  
Anil Mishra ◽  
Simon P. Hogan ◽  
Eric B. Brandt ◽  
Marc E. Rothenberg

Abstract The gastrointestinal immune system is traditionally thought to be composed of lymphocytes located within Peyer's patches and the lamina propria. We have recently reported that eosinophils also reside in the gastrointestinal tract during healthy states, in particular, within the lamina propria, and that these cells substantially increase after oral allergen exposure. We now demonstrate the presence of eosinophils in Peyer's patches and characterize the signals that regulate the accumulation of eosinophils in Peyer's patches. In contrast to the lamina propria, intestinal Peyer's patches have very low levels of eosinophils under healthy states. However, elevated levels of interleukin-5 (IL-5), generated by transgenic or pharmacologic approaches, result in a dramatic increase in eosinophil levels in Peyer's patches. Most eosinophils are located in the outer cortex and interfollicular regions of the Peyer's patches. To dissect the mechanism of eosinophil trafficking to Peyer's patches, the role of eotaxin was examined. Mice transgenic for IL-5 and genetically deficient in eotaxin were found to have reduced levels of eosinophils in Peyer's patches compared with IL-5-transgenic mice. To prove that eosinophils also traffic to Peyer's patches in wild-type mice, allergic hypersensitivity was induced and Peyer's patches were examined. Exposure to mucosal allergen promoted marked accumulation of eosinophils in Peyer's patches and this process was attenuated in eotaxin-deficient mice. In summary, these data demonstrate that elevated levels of IL-5 and mucosal allergen exposure promote eotaxin-dependent eosinophil trafficking to Peyer's patches. These studies suggest that eosinophils may cooperate with lymphocytes in the development of mucosal immune responses in the gastrointestinal tract.


2019 ◽  
Vol 2019 ◽  
pp. 1-16 ◽  
Author(s):  
B. E. Martínez-Carrillo ◽  
C. A. Rosales-Gómez ◽  
N. Ramírez-Durán ◽  
A. A. Reséndiz-Albor ◽  
J. A. Escoto-Herrera ◽  
...  

The consumption of sweeteners has increased as a measure to reduce the consumption of calories and thus combat obesity and diabetes. Sweeteners are found in a large number of products, so chronic consumption has been little explored. The objective of the study was to evaluate the effect of chronic sweetener consumption on the microbiota and immunity of the small intestine in young mice. We used 72 CD1 mice of 21 days old, divided into 3 groups: (i) No treatment, (ii) Group A (6 weeks of treatment), and (iii) Group B (12 weeks of treatment). Groups A and B were divided into 4 subgroups: Control (CL), Sucrose (Suc), Splenda® (Spl), and Svetia® (Sv). The following were determined: anthropometric parameters, percentage of lymphocytes of Peyer’s patches and lamina propria, IL-6, IL-17, leptin, resistin, C-peptide, and TNF-α. From feces, the microbiota of the small intestine was identified. The BMI was not modified; the mice preferred the consumption of Splenda® and Svetia®. The percentage of CD3+ lymphocytes in Peyer’s patches was increased. In the lamina propria, Svetia® increased the percentage of CD3+ lymphocytes, but Splenda® decreases it. The Splenda® and Svetia® subgroups elevate leptin, C-peptide, IL-6, and IL-17, with reduction of resistin. The predominant genus in all groups was Bacillus. The chronic consumption of sweeteners increases the population of lymphocytes in the mucosa of the small intestine. Maybe, Bacillus have the ability to adapt to sweeteners regardless of the origin or nutritional contribution of the same.


PLoS ONE ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. e0163607 ◽  
Author(s):  
Masatoshi Morikawa ◽  
Satoshi Tsujibe ◽  
Junko Kiyoshima-Shibata ◽  
Yohei Watanabe ◽  
Noriko Kato-Nagaoka ◽  
...  

2015 ◽  
Vol 49 ◽  
pp. e34
Author(s):  
A. Resendiz Albor ◽  
M. Salas-Pimentel ◽  
I. Arciniega-Martinez ◽  
A. García-Fonseca ◽  
E. Martinez-Becerril ◽  
...  

2007 ◽  
Vol 19 (4) ◽  
pp. 435-446 ◽  
Author(s):  
K. Kiriya ◽  
N. Watanabe ◽  
A. Nishio ◽  
K. Okazaki ◽  
M. Kido ◽  
...  

2015 ◽  
Vol 148 (4) ◽  
pp. S-10
Author(s):  
Charlotte Cordonnier ◽  
Jonathan Thévenot ◽  
Lucie Etienne-Mesmin ◽  
Amandine Rougeron ◽  
Sandra Renier ◽  
...  

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