Identification of Macrophage Genotype and Key Biological Pathways in Circulating Angiogenic Cell Transcriptome

Circulating angiogenic cells (CAC) have been identified as important regulators of vascular biology. However, there is still considerable debate about the genotype and function of CAC.

Data from publicly available gene expression data sets were used to analyse the transcriptome of in vitro cultured CAC (CAC_iv). Genes and pathways of interest were further evaluated using qPCR comparing CAC_iv versus CD14⁺ monocytic cells. The CAC_iv transcriptome strongly related to tissue macrophages, and more specifically to regulatory M2c macrophages. The cytokine expression profile of CAC_iv was predominantly immune modulatory and resembled the cytokine expression of tumor-associated macrophages (TAM). Pathway analysis revealed previously unrecognized biological processes in CAC_iv, such as riboflavin metabolism and liver X receptor (LXR)/retinoid X receptor (RXR) and farnesoid X receptor (FXR)/retinoid X receptor (RXR) pathways. Analysis of endothelial-specific genes did not show evidence for endothelial transdifferentiation.

CAC_iv are genotypically similar to regulatory M2c macrophages and lack signs of endothelial differentiation.