Yosef Nejla, Vadakkan Tegy J, Park June-Hee, Poché Ross A, Thomas Jean-Leon, Dickinson Mary E
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
Department of Neurology, Yale University, New Haven, CT, USA.
Dev Biol. 2018 Oct 1;442(1):138-154. doi: 10.1016/j.ydbio.2018.07.009. Epub 2018 Jul 30.
Macrophages are well characterized as immune cells. However, in recent years, a multitude of non-immune functions have emerged many of which play essential roles in a variety of developmental processes (Wynn et al., 2013; DeFalco et al., 2014). In adult animals, macrophages are derived from circulating monocytes originating in the bone marrow, but much of the tissue-resident population arise from erythro-myeloid progenitors (EMPs) in the extra-embryonic yolk sac, appearing around the same time as primitive erythroblasts (Schulz et al., 2012; Kierdorf et al., 2013; McGrath et al., 2015; Gomez Perdiguero et al., 2015; Mass et al., 2016). Of particular interest to our group, macrophages have been shown to act as pro-angiogenic regulators during development (Wynn et al., 2013; DeFalco et al., 2014; Hsu et al., 2015), but there is still much to learn about these early cells. The goal of the present study was to isolate and expand progenitors of yolk-sac-derived Embryonic Macrophages (EMs) in vitro to generate a new platform for mechanistic studies of EM differentiation. To accomplish this goal, we isolated pure (>98%) EGFP populations by flow cytometry from embryonic day 9.5 (E9.5) Csf1r-EGFP mice, then evaluated the angiogenic potential of EMs relative to Bone Marrow-Derived Macrophages (BMDMs). We found that EMs expressed more pro-angiogenic and less pro-inflammatory macrophage markers than BMDMs. EMs also promoted more endothelial cell (EC) cord formation in vitro, as compared to BMDMs in a manner that required direct cell-to-cell contact. Importantly, EMs preferentially matured into microglia when co-cultured with mouse Neural Stem/Progenitor Cells (NSPCs). In conclusion, we have established a protocol to isolate and propagate EMs in vitro, have further defined specialized properties of yolk-sac-derived macrophages, and have identified EM-EC and EM-NSPC interactions as key inducers of EC tube formation and microglial cell maturation, respectively.
巨噬细胞作为免疫细胞已得到充分表征。然而,近年来,其众多非免疫功能不断涌现,其中许多功能在多种发育过程中发挥着重要作用(Wynn等人,2013年;DeFalco等人,2014年)。在成年动物中,巨噬细胞源自骨髓中的循环单核细胞,但大部分组织驻留群体则来自胚外卵黄囊中的红髓系祖细胞(EMPs),与原始成红细胞同时出现(Schulz等人,2012年;Kierdorf等人,2013年;McGrath等人,2015年;Gomez Perdiguero等人,2015年;Mass等人,2016年)。我们团队特别感兴趣的是,巨噬细胞在发育过程中已被证明可作为促血管生成调节因子(Wynn等人,2013年;DeFalco等人,2014年;Hsu等人,2015年),但对于这些早期细胞仍有许多有待了解之处。本研究的目的是在体外分离并扩增卵黄囊来源的胚胎巨噬细胞(EMs)祖细胞,以建立一个用于EM分化机制研究的新平台。为实现这一目标,我们通过流式细胞术从胚胎第9.5天(E9.5)的Csf1r - EGFP小鼠中分离出纯度大于98%的EGFP群体,然后评估EMs相对于骨髓来源巨噬细胞(BMDMs)的血管生成潜力。我们发现,与BMDMs相比,EMs表达更多的促血管生成巨噬细胞标志物,而促炎巨噬细胞标志物较少。与BMDMs相比,EMs在体外还能促进更多的内皮细胞(EC)索形成,且这种促进作用需要细胞间的直接接触。重要的是,当与小鼠神经干细胞/祖细胞(NSPCs)共培养时,EMs优先成熟为小胶质细胞。总之,我们建立了一种在体外分离和扩增EMs的方法,进一步明确了卵黄囊来源巨噬细胞的特殊性质,并确定EM - EC和EM - NSPC相互作用分别是EC管形成和小胶质细胞成熟的关键诱导因素。