Figure 2
Figure 2. Heterogeneity of the phenotypic myeloid progenitor pool in NHD13 mice. Bone marrow (BM) was harvested from 25-week-old male and female NHD13 (n = 5) and WT (n = 4) littermates via the crushing technique. BM was analyzed for progenitor frequencies via flow cytometry. (A) Representative flow cytometric gating schema on the whole BM from a 25-week-old WT mouse in which common lymphoid progenitors (CLPs) (Lin−/Flt3+/IL7R+) and myeloid progenitors (MPs) (Lin−/c-Kit+/Sca1−) are a subset of the lineage-negative (live) cell population, the latter of which can be divided into common myeloid progenitors (CMPs) (FcγR−/CD34+), megakaryocyte-erythrocyte progenitors (MEPs) (FcγR−/CD34−), and granulocyte-macrophage progenitors (GMPs) (FcγR+/CD34+). (B-D) Quantification of progenitor populations in WT compared with NHD13 littermates. In all graphs, each dot represents an individual mouse, and color denotes the same individual mouse in each gate. *P < .05; ***P < .001.

Heterogeneity of the phenotypic myeloid progenitor pool in NHD13 mice. Bone marrow (BM) was harvested from 25-week-old male and female NHD13 (n = 5) and WT (n = 4) littermates via the crushing technique. BM was analyzed for progenitor frequencies via flow cytometry. (A) Representative flow cytometric gating schema on the whole BM from a 25-week-old WT mouse in which common lymphoid progenitors (CLPs) (Lin/Flt3+/IL7R+) and myeloid progenitors (MPs) (Lin/c-Kit+/Sca1) are a subset of the lineage-negative (live) cell population, the latter of which can be divided into common myeloid progenitors (CMPs) (FcγR/CD34+), megakaryocyte-erythrocyte progenitors (MEPs) (FcγR/CD34), and granulocyte-macrophage progenitors (GMPs) (FcγR+/CD34+). (B-D) Quantification of progenitor populations in WT compared with NHD13 littermates. In all graphs, each dot represents an individual mouse, and color denotes the same individual mouse in each gate. *P < .05; ***P < .001.

Close Modal

or Create an Account

Close Modal
Close Modal