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. 2011 Oct;25(10):3344–3355. doi: 10.1096/fj.10-178939

Figure 3.

Figure 3.

Ccl2−/− mice showed impaired MO/MP recruitment from bone marrow to blood and from blood to injured muscles, less severe than seen in Ccr2−/− mice. A) Flow cytometry at baseline showed that numbers of 7/4+Ly-6G MOs/MPs (a, b) were increased in bone marrow but reduced in blood (a, c) in Ccl2−/− mice (n=15), and more so in Ccr2−/− mice (n=15), as compared with wild-type controls (n=15). B) At d 3 postinjury, numbers of 7/4+Ly-6G MOs/MPs were also increased in bone marrow (a, b) and reduced in blood (a, c) in Ccl2−/− mice (n=12), and more so in Ccr2−/− mice (n=13), as compared with wild-type controls (n=15). C) Flow cytometry at d 3 showed that the numbers of F4/80+ MOs/MPs were reduced in blood and in injured muscles of Ccl2−/− mice (n=15) and more severely reduced in Ccr2−/− mice (n=15) as compared with wild-type controls (n=15), among which the Ly-6C+, but not the Ly-6C, subset was significantly reduced in blood (a, b). However, both Ly-6C+ and Ly-6C subsets were significantly reduced in injured muscles of Ccl2−/− mice and more severely reduced in Ccr2−/− mice (a, c). *P < 0.05; **P < 0.01; ***P < 0.001.