Laboratory of Food Environmental Science, Division of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Kitashirakawa-Oiwake-cho, Sakyo-ku, Kyoto, Kyoto, 606-8502, Japan.
Cytotechnology. 2012 May;64(3):221-30. doi: 10.1007/s10616-011-9351-z. Epub 2011 Apr 21.
Two critical periods of maximum exposure to antigens occur in young mammals, immediately after birth and at weaning, as a result of colonization by commensal bacteria and the ingestion of new diets. At weaning, active immune responses of antibody production against dietary proteins are known to occur, but simultaneously, oral tolerance is acquired for harmless food proteins. However, regulated mechanisms of the immune system at weaning remain to be elucidated although its immune responses may be somewhat similar to those in adulthood. Considering that tolerogenic antigen-presenting cells (APCs) are likely to be a key factor in the acquisition of oral tolerance, in the present study, we examined the changes of dendritic cells (DCs) in the lamina propria (LP) on exposure to food proteins at weaning. C57BL/6 female mice were weaned at the age of 3 weeks and orally administered 10 mg of ovalbumin (OVA) for ten consecutive days after weaning. The administration led to a decrease in the plasma level of immunoglobulin specific for OVA, suggesting the acquisition of oral tolerance. The uptake of fluorescence-labeled OVA was significantly observed for CD11c(+)LPDCs. When we analyzed the changes of two types of LPDCs, PDCA-1(+) MHC II(+) DCs and CD103(+) MHC II(+) DCs, ten consecutive gavages of OVA marginally, but not significantly, augmented only the frequency of PDCA-1(+) MHC II(+) DCs. Considering that the change of APCs likely appears immediately on the response to antigen intake, we found the statistically significant increase in the frequency of PDCA-1(+) DCs, but not in that of CD103(+) DCs, even after two treatments, indicating PDCA-1(+) DCs to be recruited in the LP within 2 days of exposure to food proteins. These results suggest that the behavior of tolerogenic PDCA-1(+) DCs may change at weaning with the removal of the immunoprotective components of maternal milk.
两个抗原暴露的关键时期发生在幼年哺乳动物身上,一个是出生后不久,另一个是断奶时,这是由于共生细菌的定植和新饮食的摄入。在断奶时,已知会发生针对膳食蛋白的抗体产生的主动免疫反应,但同时,对无害食物蛋白也会获得口服耐受。然而,尽管断奶时的免疫反应可能与成年时有些相似,但调节免疫系统的机制仍有待阐明。考虑到耐受原性抗原呈递细胞(APC)可能是获得口服耐受的关键因素,在本研究中,我们研究了断奶时暴露于食物蛋白后固有层中树突状细胞(DC)的变化。C57BL/6 雌性小鼠在 3 周龄时断奶,并在断奶后连续 10 天每天口服 10mg 卵清蛋白(OVA)。给药导致针对 OVA 的免疫球蛋白血浆水平降低,表明获得了口服耐受。CD11c(+)LPDC 显著摄取荧光标记的 OVA。当我们分析两种 LPDC(PDCA-1(+)MHC II(+)DC 和 CD103(+)MHC II(+)DC)的变化时,连续 10 次 OVA 灌胃仅略微但无显著增加 PDCA-1(+)MHC II(+)DC 的频率。考虑到 APC 的变化可能会在对抗原摄入的反应中立即出现,我们发现 PDCA-1(+)DC 的频率在统计学上显著增加,但 CD103(+)DC 的频率没有增加,即使在两次处理后,这表明 PDCA-1(+)DC 在暴露于食物蛋白后的 2 天内就被招募到 LP 中。这些结果表明,断奶时耐受原性 PDCA-1(+)DC 的行为可能会因母体乳汁中免疫保护成分的去除而发生变化。