Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada; The Pirbright Institute, Pirbright, Woking, GU24 0NF, UK.
The Pirbright Institute, Pirbright, Woking, GU24 0NF, UK.
Vet Immunol Immunopathol. 2021 Apr;234:110215. doi: 10.1016/j.vetimm.2021.110215. Epub 2021 Feb 25.
Dendritic cells (DCs) are the most potent antigen presenting cells (APCs). Because of the difficulty in obtaining these cells directly from tissues, different sources of DCs are frequently used for in vitro experimentation and many of their biological and functional characteristics were studied using these systems. Until recently, it was assumed that specific culture conditions polarized the differentiation of either DCs or macrophages (Macs); however, it was shown that some DC culture systems in other species generate heterogeneous cell populations that can be identified according to their CD11c and MHC class II (MHC-II) expression. Following this approach, porcine DCs were directly isolated from peripheral blood or differentiated in vitro by culturing bone marrow (BM) progenitor cells or blood monocytes treated with growth factors. Mostly homogeneous monocyte-derived DCs (MoDCs) were obtained with similar phenotype and phagocytic characteristics to that of blood DCs. On the contrary, BM-derived DC (BMDC) cultures generated two distinct heterogeneous populations identified as MHC-II and MHC-II cells. BMDCs MHC-II had similar phenotypic and phagocytic characteristics to those of MoDCs and blood DCs. However, BMDCs MHC-II population expressed a higher amount of surface markers and transcribed genes associated with Macs-lineage exhibiting a higher phagocytic capacity than all the other cells. Noteworthy, every cell system expressed different genetic signatures. These results will help interpreting and re-interpreting data obtained using in vitro systems.
树突状细胞 (DCs) 是最有效的抗原提呈细胞 (APCs)。由于直接从组织中获取这些细胞较为困难,因此经常使用不同来源的 DC 用于体外实验,并使用这些系统研究其许多生物学和功能特性。直到最近,人们还认为特定的培养条件会使 DC 或巨噬细胞 (Macs) 的分化发生极化;然而,已经表明,其他物种的一些 DC 培养系统会产生异质细胞群体,可以根据其 CD11c 和 MHC 类 II (MHC-II) 表达来识别。采用这种方法,可直接从外周血中分离猪 DC,或通过培养骨髓 (BM) 祖细胞或用生长因子处理的血液单核细胞在体外分化。通过这种方法获得的主要是单核细胞来源的 DC (MoDCs),其表型和吞噬特性与血液 DC 相似。相反,BM 来源的 DC (BMDC) 培养物产生了两种不同的异质群体,分别被鉴定为 MHC-II 和 MHC-II 细胞。BMDCs MHC-II 具有与 MoDCs 和血液 DCs 相似的表型和吞噬特性。然而,BMDCs MHC-II 群体表达更高数量的与 Macs 谱系相关的表面标志物和转录基因,表现出比所有其他细胞更高的吞噬能力。值得注意的是,每个细胞系统都表达不同的遗传特征。这些结果将有助于解释和重新解释使用体外系统获得的数据。