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. 2009 May 6;13(9b):3720–3729. doi: 10.1111/j.1582-4934.2009.00785.x

Figure 3.

Figure 3

Phenotypic characterization of CPCs. LSR-II flow cytometric analyses of (gated, a) mononuclear cells in peripheral blood, identified a distinct population of CPCs that co-express VEGFR2 and PDGFRβ (c); single-colour controls were used for compensation (e.g. see staining for PDGFRβ-Alexa Fluor 647 in b). These CPCs (in blue) are positive for CD45 (d) and show scattering properties typical of small cells with a high nucleus to cytoplasm ratio (a, d). A subset of CPCs is positive for CD11b (e), whereas all VEGFR2+PDGFRβ+ CPCs are positive for CD31 (f); CPCs are distinct from cells with a phenotype consistent with ‘circulating ECs’, i.e. CD31+CD45 (see gated population in f).