The phenotypic and functional properties of mouse yolk-sac-derived embryonic macrophages.

Dev Biol

Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Cardiovascular Research Institute, Baylor College of Medicine, Houston, TX, USA; Department of Bioengineering, Rice University, Houston, TX, USA. Electronic address:

Published: October 2018

AI Article Synopsis

  • Macrophages, traditionally known for their immune functions, also play vital roles in developmental processes, with a significant proportion arising from yolk-sac progenitors rather than just bone marrow.
  • This study aimed to isolate and expand these yolk-sac-derived embryonic macrophages (EMs) in vitro to better understand their development and functions.
  • Findings revealed that EMs promote more endothelial cell cord formation and have unique maturation pathways compared to bone marrow-derived macrophages (BMDMs), highlighting their specialized roles in angiogenesis and neural development.

Article Abstract

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190604PMC
http://dx.doi.org/10.1016/j.ydbio.2018.07.009DOI Listing

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