Camps-Bossacoma Mariona, Pérez-Cano Francisco J, Franch Àngels, Untersmayr Eva, Castell Margarida
Section of Physiology, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028, Barcelona, Spain; Nutrition and Food Safety Research Institute (INSA-UB), 08921 Santa Coloma de Gramenet, Spain; Institute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, A-1090, Vienna, Austria.
Section of Physiology, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028, Barcelona, Spain; Nutrition and Food Safety Research Institute (INSA-UB), 08921 Santa Coloma de Gramenet, Spain.
J Nutr Biochem. 2017 Apr;42:182-193. doi: 10.1016/j.jnutbio.2017.01.005. Epub 2017 Jan 23.
Previous studies have attributed to the cocoa powder the capacity to attenuate the immune response in a rat oral sensitization model. To gain a better understanding of cocoa-induced mechanisms at small intestinal level, 3-week-old female Lewis rats were fed either a standard diet or a diet containing 10% cocoa for 4 weeks with or without concomitant oral sensitization with ovalbumin (OVA). Thereafter, we evaluated the lymphocyte composition of the Peyer's patches (PPL), small intestine epithelium (IEL) and lamina propria (LPL). Likewise, gene expression of several immune molecules was quantified in the small intestine. Moreover, histological samples were used to evaluate the proportion of goblet cells, IgA+ cells and granzyme+cells as well. In cocoa-fed animals, we identified a five-time reduction in the percentage of IgA+ cells in intestinal tissue together with a decreased proportion of TLR4+ IEL. Analyzing the lymphocyte composition, almost a double proportion of TCRγδ+cells and an increase of NK cell percentage in PPL and IEL were found. In addition, a rise in CD25+, CD103+ and CD62L- cell proportions was observed in CD4+ PPL from cocoa-fed animals, along with a decrease in gene expression of CD11b, CD11c and IL-10. These results suggest that changes in PPL and IEL composition and in the gene expression induced by the cocoa diet could be involved, among other mechanisms, on its tolerogenic effect.
先前的研究认为可可粉具有在大鼠口服致敏模型中减弱免疫反应的能力。为了更好地了解可可在小肠水平诱导的机制,给3周龄雌性Lewis大鼠喂食标准饮食或含10%可可的饮食4周,同时给予或不给予卵清蛋白(OVA)口服致敏。此后,我们评估了派尔集合淋巴结(PPL)、小肠上皮(IEL)和固有层(LPL)的淋巴细胞组成。同样,还对小肠中几种免疫分子的基因表达进行了定量分析。此外,组织学样本也用于评估杯状细胞、IgA+细胞和颗粒酶+细胞的比例。在喂食可可的动物中,我们发现肠道组织中IgA+细胞的百分比降低了五倍,同时TLR4+ IEL的比例也有所下降。分析淋巴细胞组成发现,PPL和IEL中TCRγδ+细胞的比例几乎增加了一倍,NK细胞百分比也有所增加。此外,在喂食可可的动物的CD4+ PPL中,观察到CD25+、CD103+和CD62L-细胞比例升高,同时CD11b、CD11c和IL-10的基因表达下降。这些结果表明,可可饮食诱导的PPL和IEL组成变化以及基因表达变化,可能通过其他机制参与其免疫耐受作用。