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Oral Serum-Derived Bovine Immunoglobulin/Protein Isolate Has Immunomodulatory Effects on the Colon of Mice that Spontaneously Develop Colitis

机译:口服血清牛免疫球蛋白/蛋白质分离物对自发性结肠炎的小鼠结肠具有免疫调节作用

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摘要

Dietary immunoglobulin concentrates prepared from animal plasma can modulate the immune response of gut-associated lymphoid tissue (GALT). Previous studies have revealed that supplementation with serum-derived bovine immunoglobulin/protein isolate (SBI) ameliorates colonic barrier alterations in the mdr1a-/- genetic mouse model of IBD. Here, we examine the effects of SBI on mucosal inflammation in mdr1a-/- mice that spontaneously develop colitis. Wild type (WT) mice and mice lacking the mdr1a gene (KO) were fed diets supplemented with either SBI (2% w/w) or milk proteins (Control diet), from day 21 (weaning) until day 56. Leucocytes in mesenteric lymph nodes (MLN) and in lamina propria were determined, as was mucosal cytokine production. Neutrophil recruitment and activation in MLN and lamina propria of KO mice were increased, but were significantly reduced in both by SBI supplementation (p < 0.05). The increased neutrophil recruitment and activation observed in KO mice correlated with increased colon oxidative stress (p < 0.05) and SBI supplementation reduced this variable (p < 0.05). The Tact/Treg lymphocyte ratios in MLN and lamina propria were also increased in KO animals, but SBI prevented these changes (both p < 0.05). In the colon of KO mice, there was an increased production of mucosal pro-inflammatory cytokines such as IL-2 (2-fold), IL-6 (26-fold) and IL-17 (19-fold), and of chemokines MIP-1β (4.5-fold) and MCP-1 (7.2-fold). These effects were significantly prevented by SBI (p < 0.05). SBI also significantly increased TGF-β secretion in the colon mucosa, suggesting a role of this anti-inflammatory cytokine in the modulation of GALT and the reduction of the severity of the inflammatory response during the onset of colitis.
机译:从动物血浆中制备的膳食免疫球蛋白浓缩物可以调节肠道相关淋巴样组织(GALT)的免疫反应。先前的研究表明,补充血清来源的牛免疫球蛋白/蛋白质分离物(SBI)可以改善IBD的mdr1a-/-遗传小鼠模型中的结肠屏障改变。在这里,我们检查了SBI对自发发展为结肠炎的mdr1a-/-小鼠黏膜炎症的影响。从第21天(断奶)到第56天,给野生型(WT)小鼠和缺少mdr1a基因(KO)的小鼠饲喂补充SBI(2%w / w)或乳蛋白(对照饮食)的饮食。肠系膜白细胞确定了淋巴结(MLN)和固有层,以及粘膜细胞因子的产生。 KO小鼠的MLN和固有层的中性粒细胞募集和激活均增加,但通过SBI补充均显着降低(P <0.05)。在KO小鼠中观察到的中性粒细胞募集和激活的增加与结肠氧化应激的增加相关(p <0.05),而SBI的补充减少了该变量(p <0.05)。在KO动物中,MLN和固有层中的Tact / Treg淋巴细胞比率也增加了,但是SBI阻止了这些改变(均p <0.05)。在KO小鼠的结肠中,粘膜促炎细胞因子的产生增加,例如IL-2(2倍),IL-6(26倍)和IL-17(19倍)以及趋化因子的产生。 MIP-1β(4.5倍)和MCP-1(7.2倍)。 SBI显着预防了这些影响(p <0.05)。 SBI还显着增加了结肠粘膜中TGF-β的分泌,表明该抗炎细胞因子在结肠炎发作期间调节GALT和减轻炎症反应的严重性方面具有作用。

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