Figure 1.
Loss of STAT1 affects the stem and progenitor compartment in steady-state hematopoiesis. (A) Dot plot showing normalized STAT1 expression in cell types across the Dahlin landscape. The size of each dot indicates the proportion of cells with normalized expression level >0, and the color intensity shows the levels of STAT1 expression. (B) Violin plots showing normalized STAT1 expression in immature cell types in Nestorowa’s scRNA-seq dataset. Mean ± standard deviation indicated in overlaid box. (C) The frequency of T cells was reduced in STAT1-deficient bone marrow. (D) The frequency of pre-granulocyte-macrophage progenitors (PreGM) was increased in STAT1-deficient bone marrow. Flow cytometry was performed, and PreGM progenitors were defined as Lin−Sca1−cKit+CD41−CD16/32−CD105−CD150−. (E) The frequencies of MPP3 and MPP4 were reduced in STAT1-deficient bone marrow. Flow cytometry was performed, and multipotent progenitor MPPs were defined as the following: MPP1 (Flk2−CD150+CD48−LSK), MPP2 (Flk2−CD150+CD48+LSK), MPP3 (Flk2−CD150−CD48+LSK), and MPP4 (Flk2+CD150−CD48+LSK). (F) The frequency of ESLAM HSCs was increased in STAT1-deficient mice. Bone marrow ESLAM HSCs were defined as CD45+CD150+CD48−EPCR+ cells. Data are shown as mean ± standard error; asterisks indicate significant differences by Student t test (∗P < .05; ∗∗P < .01).

Loss of STAT1 affects the stem and progenitor compartment in steady-state hematopoiesis. (A) Dot plot showing normalized STAT1 expression in cell types across the Dahlin landscape. The size of each dot indicates the proportion of cells with normalized expression level >0, and the color intensity shows the levels of STAT1 expression. (B) Violin plots showing normalized STAT1 expression in immature cell types in Nestorowa’s scRNA-seq dataset. Mean ± standard deviation indicated in overlaid box. (C) The frequency of T cells was reduced in STAT1-deficient bone marrow. (D) The frequency of pre-granulocyte-macrophage progenitors (PreGM) was increased in STAT1-deficient bone marrow. Flow cytometry was performed, and PreGM progenitors were defined as LinSca1cKit+CD41CD16/32CD105CD150. (E) The frequencies of MPP3 and MPP4 were reduced in STAT1-deficient bone marrow. Flow cytometry was performed, and multipotent progenitor MPPs were defined as the following: MPP1 (Flk2CD150+CD48LSK), MPP2 (Flk2CD150+CD48+LSK), MPP3 (Flk2CD150CD48+LSK), and MPP4 (Flk2+CD150CD48+LSK). (F) The frequency of ESLAM HSCs was increased in STAT1-deficient mice. Bone marrow ESLAM HSCs were defined as CD45+CD150+CD48EPCR+ cells. Data are shown as mean ± standard error; asterisks indicate significant differences by Student t test (∗P < .05; ∗∗P < .01).

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