Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, 31270-901 Belo Horizonte, MG, Brazil.
Immunobiology. 2011 Oct;216(10):1085-93. doi: 10.1016/j.imbio.2011.05.007. Epub 2011 May 14.
Aging is reported to be associated with decline in oral tolerance induction, which is initiated at the intestinal mucosal surface. Herein, we examined the effect of aging in T cells and cytokines at the intestinal mucosa that might be involved in oral tolerance induction. Frequencies of regulatory-type IEL subsets such as TCRγδ(+) and TCRαβ(+)CD8αα(+) were lower in aged mice. Mucosal CD4(+)CD25(+)Foxp3(+) and CD4(+)LAP(+) T cells increased with aging but activated CD44(+)CD4(+) mucosal T cells also augmented. Production of TGF-β and IL-10 in the small intestine of old mice was reduced. Moreover, the ability of mucosal dendritic cells of aged mice to stimulate TGF-β secretion and differentiation of CD4(+)LAP(+) T cells in co-culture studies also declined with aging. Reduction in these regulatory-type cytokines and T cells may help to explain the decline in susceptibility to oral induction during aging. However, not all mucosal regulatory elements were altered by aging and CD4(+)CD25(+)Foxp3(+) T cells were especially resistant to changes. Persistence of some mechanisms of regulation may play a critical role in maintaining mucosal homeostasis during aging.
衰老是与口腔耐受诱导的下降有关,口腔耐受诱导始于肠道黏膜表面。在此,我们研究了衰老对肠道黏膜 T 细胞和细胞因子的影响,这些 T 细胞和细胞因子可能参与了口腔耐受诱导。在老年小鼠中,调节型 IEL 亚群(如 TCRγδ(+)和 TCRαβ(+)CD8αα(+))的频率较低。黏膜 CD4(+)CD25(+)Foxp3(+)和 CD4(+)LAP(+)T 细胞随年龄增长而增加,但激活的 CD44(+)CD4(+)黏膜 T 细胞也增加了。老年小鼠小肠中 TGF-β和 IL-10 的产生减少。此外,在共培养研究中,老年小鼠黏膜树突状细胞刺激 TGF-β分泌和 CD4(+)LAP(+)T 细胞分化的能力也随衰老而下降。这些调节型细胞因子和 T 细胞的减少可能有助于解释衰老过程中对口腔诱导的敏感性下降。然而,并非所有黏膜调节因子都随衰老而改变,CD4(+)CD25(+)Foxp3(+)T 细胞尤其不易受影响。一些调节机制的持续存在可能在衰老过程中维持黏膜稳态中发挥关键作用。