Faculty of Medicine, Biomedical Center (BMC), Institute for Immunology, LMU Munich, Planegg-Martinsried, Germany.
Life and Medical Sciences Institute, Bonn, Germany.
Front Immunol. 2019 Feb 12;10:222. doi: 10.3389/fimmu.2019.00222. eCollection 2019.
Apoptotic cell death of Dendritic cells (DCs) is critical for immune homeostasis. Although intrinsic mechanisms controlling DC death have not been fully characterized up to now, experimentally enforced inhibition of DC-death causes various autoimmune diseases in model systems. We have generated mice deficient for (Ppef2), which is selectively expressed in CD8 DCs, but not in other related DC subtypes such as tissue CD103 DCs. Ppef2 is down-regulated rapidly upon maturation of DCs by toll-like receptor stimuli, but not upon triggering of CD40. Ppef2-deficient CD8 DCs accumulate the pro-apoptotic (Bim) and show increased apoptosis and reduced competitve repopulation capacities. Furthermore, CD8 DCs have strongly diminished antigen presentation capacities , as CD8 T cells primed by CD8 DCs undergo reduced expansion. In conclusion, our data suggests that Ppef2 is crucial to support survival of immature CD8 DCs, while Ppef2 down-regulation during DC-maturation limits T cell responses.
树突状细胞 (DC) 的凋亡性细胞死亡对于免疫稳态至关重要。尽管控制 DC 死亡的内在机制尚未得到充分描述,但在模型系统中,实验性地抑制 DC 死亡会导致各种自身免疫性疾病。我们已经生成了缺乏 (Ppef2) 的小鼠,Ppef2 选择性地在 CD8 DC 中表达,但不在其他相关的 DC 亚型(如组织 CD103 DC)中表达。Ppef2 在 DC 被 Toll 样受体刺激成熟时迅速下调,但在触发 CD40 时不会下调。缺乏 Ppef2 的 CD8 DC 积累促凋亡的 (Bim),并表现出增加的凋亡和减少的竞争再殖能力。此外, CD8 DC 的抗原呈递能力显著降低 ,因为由 CD8 DC 激活的 CD8 T 细胞经历了减少的扩增。总之,我们的数据表明 Ppef2 对于支持未成熟 CD8 DC 的存活至关重要,而在 DC 成熟过程中 Ppef2 的下调限制了 T 细胞反应。