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. Author manuscript; available in PMC: 2011 Jul 1.
Published in final edited form as: Nat Med. 2010 Dec 19;17(1):87–95. doi: 10.1038/nm.2278

Figure 2. CD11b+Ly6G+ IMCs are the predominant source of Hdc-EGFP expression in the bone marrow.

Figure 2

(a) The left panel shows the percentage of EGFP+ cells within the bone marrow (BM), spleen, and peripheral blood of Hdc-EGFP mice; the right panel shows the relative proportion of CD11b+ and Gr-1+ cells gated from the EGFP+ subset respectively.

(b) Expression of CD11b+Ly6G+ cells. CD11b+Gr-1+ myeloid cells were gated from the bone marrow of Hdc-EGFP mice. FACS analysis here indicates the proportion of EGFP+ cells that were CD11b+Gr-1+Ly6Ghigh, CD11b+Gr-1+Ly6Gmid, and CD11b+Gr-1+Ly6G cells. This figure shows representative data from five experiments.

(c) Analysis of peritoneal exudative cells (PECs). Approximately 12% of EGFP+ were detected in the PEC by FACS. CD11b+Gr-1+ (28%) and CD11b+Gr-1 (47%) myeloid cells were the major EGFP+ cells. Approximately 15% of EGFP+ cells expressed mast cell markers: c-kit+FcεR+.

(d) Differentiation of splenic Hdc-EGFP+ IMCs. Immunofluorescence of DAPI stained EGFP+ CD11b+Ly6G+ IMCs treated with or without G-CSF for 48 hours showed suppression of EGFP expression with granulocyte differentiation (The pictures show representative data from three independent experiments).