Department of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2013 Oct 3;8(10):e76801. doi: 10.1371/journal.pone.0076801. eCollection 2013.
We have investigated the effect of different maturation stimuli on the ability of mature dendritic cells (DCs) to cross-present newly acquired particulate antigens. Cross-presentation was impaired in DCs matured by treatment with TNF-α, CpG and LPS, but was less affected upon CD40L-induced maturation. The difference could not be explained by decreased antigen uptake or translocation into the cytosol, but decreased cross-presentation ability did correlate with increased phagosomal/lysosomal acidification. Nevertheless, intra-phagosomal degradation of OVA was not increased in matured samples, suggesting that decreasing phagosomal pH may also regulate cross-presentation by a mechanism other than enhancing degradation.
我们研究了不同成熟刺激对成熟树突状细胞 (DC) 摄取新获得的颗粒性抗原并进行交叉呈递能力的影响。用 TNF-α、CpG 和 LPS 处理成熟的 DC 会损害交叉呈递,而 CD40L 诱导的成熟则影响较小。这种差异不能用抗原摄取或易位到细胞质减少来解释,但交叉呈递能力的降低与吞噬体/溶酶体酸化增加有关。然而,在成熟样本中,OVA 的内吞噬体降解并没有增加,这表明降低吞噬体 pH 值也可能通过增强降解以外的机制来调节交叉呈递。