Department of Biological Sciences, Auburn University, Auburn, Alabama.
PLoS One. 2018 May 10;13(5):e0196591. doi: 10.1371/journal.pone.0196591. eCollection 2018.
Dendritic cells (DC) are sentinels of the immune system, alerting and enlisting T cells to clear pathogenic threats. As such, numerous studies have demonstrated their effective uptake and proteolytic activities coupled with antigen processing and presentation functions. Yet, less is known about how these cellular mechanisms change and develop as myeloid cells progress from progenitor cells to more differentiated cell types such as DC. Thus, our study comparatively examined these functions at different stages of myeloid cell development driven by the GM-CSF. To measure these activities at different stages of development, GM-CSF driven bone marrow cells were sorted based on expression of Ly6C, CD115, and CD11c. This strategy enables isolation of cells representing five distinct myeloid cell types: Common Myeloid Progenitor (CMP), Granulocyte/Macrophage Progenitor (GMP), monocytes, monocyte-derived Macrophage/monocyte-derived Dendritic cell Precursors (moMac/moDP), and monocyte-derived DC (moDC). We observed significant differences in the uptake capacity, proteolysis, and antigen processing and presentation functions between these myeloid cell populations. CMP showed minimal uptake capacity with no detectable antigen processing and presenting function. The GMP population showed higher uptake capacity, modest proteolytic activity, and little T cell stimulatory function. In the monocyte population, the uptake capacity reached its peak, yet this cell type had minimal antigen processing and presentation function. Finally, moMac/moDP and moDC had a modestly decreased uptake capacity, high degradative capacity and strong antigen processing and presentation functions. These insights into when antigen processing and presentation function develop in myeloid cells during GM-CSF driven differentiation are crucial to the development of vaccines, allowing targeting of the most qualified cells as an ideal vaccine vehicles.
树突状细胞 (DC) 是免疫系统的哨兵,能够提醒并招募 T 细胞清除病原体威胁。因此,许多研究已经证明了它们在摄取和蛋白水解活性方面的有效性,以及抗原加工和呈递功能。然而,对于髓系细胞从祖细胞向更分化的细胞类型(如 DC)发展时,这些细胞机制如何变化和发展,我们知之甚少。因此,我们的研究比较了 GM-CSF 驱动的髓系细胞发育不同阶段的这些功能。为了在不同的发育阶段测量这些活性,根据 Ly6C、CD115 和 CD11c 的表达对 GM-CSF 驱动的骨髓细胞进行了分选。这种策略能够分离代表五种不同髓系细胞类型的细胞:普通髓系祖细胞 (CMP)、粒细胞/巨噬细胞祖细胞 (GMP)、单核细胞、单核细胞衍生的巨噬细胞/单核细胞衍生的树突状细胞前体 (moMac/moDP) 和单核细胞衍生的树突状细胞 (moDC)。我们观察到这些髓系细胞群体之间在摄取能力、蛋白水解、抗原加工和呈递功能方面存在显著差异。CMP 表现出最小的摄取能力,没有可检测到的抗原加工和呈递功能。GMP 群体表现出更高的摄取能力、适度的蛋白水解活性和较少的 T 细胞刺激功能。在单核细胞群体中,摄取能力达到峰值,但该细胞类型的抗原加工和呈递功能最小。最后,moMac/moDP 和 moDC 的摄取能力略有下降,降解能力高,抗原加工和呈递功能强。这些关于 GM-CSF 驱动分化过程中髓系细胞何时发展抗原加工和呈递功能的见解对于疫苗的开发至关重要,使我们能够靶向最适合的细胞作为理想的疫苗载体。