Figure 1
Figure 1. Ly6C expression marks a subset of mouse bone marrow GMPs. (A) Ly6C expression by LKS−CD34+FcγRhi cells (unsorted GMPs) was assessed by flow cytometry (see “Materials and methods” and supplemental Figure 1 for sorting and gating strategies). Data are representative of >3 independent experiments. (B-C) GMP-Ly6C− and GMP-Ly6C+ cells were FACS sorted from CD45.2 donor mouse Lin− cells and 200 000 cells were injected IV into congenic CD45.1 recipient mice (nonirradiated) on day 0. Spleens were harvested from recipient mice on days 4 and 7, and donor cell-derived (CD45.2+) neutrophils (green gates), monocytes, and macrophages (blue gates) were detected by flow cytometry (see supplemental Figure 4 for gating strategy). CD45.2+CD11b+ splenic cells are shown. Data presented are from 1 experiment that is representative of at least 3 independent experiments.

Ly6C expression marks a subset of mouse bone marrow GMPs. (A) Ly6C expression by LKSCD34+FcγRhi cells (unsorted GMPs) was assessed by flow cytometry (see “Materials and methods” and supplemental Figure 1 for sorting and gating strategies). Data are representative of >3 independent experiments. (B-C) GMP-Ly6C and GMP-Ly6C+ cells were FACS sorted from CD45.2 donor mouse Lin cells and 200 000 cells were injected IV into congenic CD45.1 recipient mice (nonirradiated) on day 0. Spleens were harvested from recipient mice on days 4 and 7, and donor cell-derived (CD45.2+) neutrophils (green gates), monocytes, and macrophages (blue gates) were detected by flow cytometry (see supplemental Figure 4 for gating strategy). CD45.2+CD11b+ splenic cells are shown. Data presented are from 1 experiment that is representative of at least 3 independent experiments.

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