Figure 3
Figure 3. Abnormal distribution of phenotypic HSCs and myeloid precursors in the bone marrow and spleen of diseased Ptpn11D61Y mice. (A,B) Flow cytometric analysis of BM and splenic (A) LK subsets, including CMPs (LK-CD34+FcγRII/IIIlo), GMPs (LK-CD34+FcγRII/III+), and MEPs (LK-CD34−FcγRII/III−) and (B) LSK subsets, LT-HSCs (LSK-Flk2−CD34−), ST-HSCs (LSK-Flk2−CD34+), and MPPs (LSK-Flk2+CD34+). Representative contour plots are shown. All values are the mean frequency of the parental gate. See Tables 1 and 2 for absolute numbers of each population. (C) LSK cells from BM or spleen of control and Ptpn11D61Y mice were purified by FACS and stained with Hoechst 33342 (H), and Pyronin Y (PY). The mean percentages of cells in G0 (H−PY−), sub-G0G1 (H−PYlo), G1 (H−PY+), and S/G2M (H+PY+) are indicated. Representative contour plots are shown (n = 3; *P < .05).

Abnormal distribution of phenotypic HSCs and myeloid precursors in the bone marrow and spleen of diseased Ptpn11D61Y mice. (A,B) Flow cytometric analysis of BM and splenic (A) LK subsets, including CMPs (LK-CD34+FcγRII/IIIlo), GMPs (LK-CD34+FcγRII/III+), and MEPs (LK-CD34FcγRII/III) and (B) LSK subsets, LT-HSCs (LSK-Flk2CD34), ST-HSCs (LSK-Flk2CD34+), and MPPs (LSK-Flk2+CD34+). Representative contour plots are shown. All values are the mean frequency of the parental gate. See Tables 1 and 2 for absolute numbers of each population. (C) LSK cells from BM or spleen of control and Ptpn11D61Y mice were purified by FACS and stained with Hoechst 33342 (H), and Pyronin Y (PY). The mean percentages of cells in G0 (HPY), sub-G0G1 (HPYlo), G1 (HPY+), and S/G2M (H+PY+) are indicated. Representative contour plots are shown (n = 3; *P < .05).

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