Savina Ariel, Amigorena Sebastian
Institut Curie, INSERM U653, Immunité et Cancer, Paris, France.
Immunol Rev. 2007 Oct;219:143-56. doi: 10.1111/j.1600-065X.2007.00552.x.
Like macrophages and neutrophils, dendritic cells (DCs) are considered professional phagocytes. Even if the three cell types phagocytose parasites, bacteria, cell debris, or even intact cells very efficiently, the functional outcomes of the phagocytic event are quite different. Macrophages and neutrophils scavenge and destroy phagocytosed particles, a critical step in innate immunity. DCs, in contrast, have developed means to 'preserve' useful information from the ingested particles that serve to initiate adaptive immune responses. Thus, both phagosomal degradation and acidification are much lower in DCs than in macrophages or neutrophils. Reduced degradation results in the conservation of antigenic peptides and in their increased presentation on major histocompatibility complex class I and II molecules. In this article, we review the mechanisms that control this delicate equilibrium between phagosomal degradation/cytotoxicity and antigen presentation in the different families of phagocytes.
与巨噬细胞和中性粒细胞一样,树突状细胞(DC)被视为专职吞噬细胞。即使这三种细胞类型都能非常有效地吞噬寄生虫、细菌、细胞碎片甚至完整细胞,但吞噬事件的功能结果却大不相同。巨噬细胞和中性粒细胞清除并破坏吞噬的颗粒,这是固有免疫中的关键步骤。相比之下,DC已发展出从摄取的颗粒中“保存”有用信息的方法,这些信息用于启动适应性免疫反应。因此,DC中的吞噬体降解和酸化程度远低于巨噬细胞或中性粒细胞。降解减少导致抗原肽得以保存,并增加其在主要组织相容性复合体I类和II类分子上的呈递。在本文中,我们综述了控制不同吞噬细胞家族中吞噬体降解/细胞毒性与抗原呈递之间这种微妙平衡的机制。