Wheat-derived arabinoxylans reduced M2-macrophage functional activity, but enhanced monocyte-recruitment capacity
文献类型： 外文期刊
作者： Govers, Coen 1 ; Tang, Yongfu 1 ; Stolte, Ellen H. 4 ; Wichers, Harry J. 1 ; Mes, Jurriaan J. 1 ;
作者机构： 1.Wageningen Univ & Res, Wageningen Food & Biobased Res, Wageningen, Netherlands
2.Wageningen Univ & Res, Lab Food Chem, Wageningen, Netherlands
3.Chinese Acad Trop Agr Sci, Agr Prod Proc Res Inst, Zhanjiang, Peoples R China
4.Wageningen Univ & Res, Anim Sci Dept, Host Microbe Interact Grp, Wageningen, Netherlands
期刊名称：FOOD & FUNCTION （ 影响因子：5.396； 五年影响因子：5.534 ）
ISSN： 2042-6496
年卷期： 2020 年 11 卷 8 期
页码：
收录情况： SCI
摘要： The immunomodulatory properties of non-digestible polysaccharides (NDPs) have been recognized inin vitroandin vivostudies. The latter mostly demonstrated altered frequencies and inflammatory status of immune cells as clinical parameters. Most of the NDP activity will be exerted in the intestine where they can directly interact with macrophages. The predominant macrophage phenotype in the intestine is M2-like, with M1-like macrophages arising during inflammation. Here, we investigated transcriptional and functional impact on these macrophage phenotypes by NDP-treatment (i.e.yeast-derived soluble beta-glucan (yeast-beta G), apple-derived RG-I (apple-RGI), shiitake-derived beta-glucan (shiitake-beta G) or wheat-derived arabinoxylan (wheat-AX)). Wheat-AX, and to a lesser extent shiitake-beta G and apple-RGI but not yeast-beta G, reduced endocytosis and antigen processing capacity of M1- and M2-like macrophages. Moreover, the NDPs, and most notably wheat-AX, strongly induced transcription and secretion of a unique set of cytokines and chemokines. Conditioned medium from wheat-AX-treated M2-like macrophages subsequently demonstrated strongly increased monocyte recruitment capacity. These findings are in line with clinically observed immunomodulatory aspects of NDPs making it tempting to speculate that clinical activity of some NDPs is mediated through enhanced chemoattraction and modifying activity of intestinal immune cells.
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