TNFΔARE Mice Display Abnormal Lymphatics and Develop Tertiary Lymphoid Organs in the Mesentery

被引:31
|
作者
Rehal, Sonia [1 ]
von der Weid, Pierre-Yves [1 ]
机构
[1] Univ Calgary, Cumming Sch Med, Snyder Inst Chron Dis, Dept Physiol & Pharmacol,Inflammat Res Network &, Calgary, AB, Canada
来源
AMERICAN JOURNAL OF PATHOLOGY | 2017年 / 187卷 / 04期
基金
加拿大健康研究院;
关键词
CROHNS-DISEASE; DENDRITIC CELLS; TISSUE; NODES; BIOSYNTHESIS; COLITIS; LYMPHANGIOGENESIS; INFLAMMATION; EXPRESSION; VESSELS;
D O I
10.1016/j.ajpath.2016.12.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Chronic inflammatory diseases are associated with a persistent and enhanced response to environmental antigens. As an adaptive response to this exaggerated immune state, affected tissue typically develops tertiary lymphoid organs. Studies of Crohn disease (CD), a chronic inflammatory disease of the intestinal tract, report tertiary lymphoid organs present within the mucosal wall, along with other lymphatic diseases, such as lymphangiogenesis and obstructed Lymphatic vessels. These observations suggest that downstream mesenteric lymphatic vessels and lymph drainage into mesenteric lymph nodes may be compromised. However, information is lacking on the morphologic features and functional status of mesenteric Lymphatics in CD. Using confocal imaging, PCR, flow cytometry, and functional strategies, we addressed these questions in the established TNF Delta ARE mouse model of CD and found that this mouse model had many lymphatic abnormalities reminiscent of human CD. These abnormalities include intestinal Lymphangiectasia, mesenteric lymph node Lymphadenopathy, and Lymphangiogenesis in both the mesentery and mucosa. Critically, TNF Delta ARE mice also present mesenteric tertiary lymphoid organs and have altered lymphatic transport of dendritic cells to mesenteric Lymph nodes, two features likely to actively modulate immunity. Our findings provide key insights into lymphatic remodeling in the TNF Delta ARE mouse model. They shed light on the involvement of these Lymphatic changes in immune dysfunctions observed in CD and suggest the Lymphatic system as new target for therapeutic options.
引用
收藏
页码:798 / 807
页数:10
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