Figure 5.
Figure 5. Common lymphoid progenitors express Hmgb3. (A) Isolation of GFP+ and GFP– common lymphoid progenitors by flow cytometry. Upper: Lin– bone marrow isolated from Hmgb3-KI mice. Middle: c-kit and Sca-1 expression in Hmgb3-KI Lin– bone marrow (left). Cells positive for c-kit and Sca-1 were selected based on isotype staining of littermate control Lin– bone marrow cells (right). Lower: IL-7Rα and GFP profiles of c-kit+/Sca-1+ cells (left). Cells were separated into IL-7Rα+ and GFP+/– populations based on isotype staining of littermate control Lin– c-kit+, Sca-1+ bone marrow cells (Right). (B) Mean CFU–pre-B cell frequency in GFP– (n = 8, 66 colonies counted) and GFP+ (n = 7, 294 colonies counted) CLP populations. Values were determined by scoring pre–B cell colonies per 500 cells cultured. P values were determined by Student t test.

Common lymphoid progenitors express Hmgb3. (A) Isolation of GFP+ and GFP common lymphoid progenitors by flow cytometry. Upper: Lin bone marrow isolated from Hmgb3-KI mice. Middle: c-kit and Sca-1 expression in Hmgb3-KI Lin bone marrow (left). Cells positive for c-kit and Sca-1 were selected based on isotype staining of littermate control Lin bone marrow cells (right). Lower: IL-7Rα and GFP profiles of c-kit+/Sca-1+ cells (left). Cells were separated into IL-7Rα+ and GFP+/– populations based on isotype staining of littermate control Lin c-kit+, Sca-1+ bone marrow cells (Right). (B) Mean CFU–pre-B cell frequency in GFP (n = 8, 66 colonies counted) and GFP+ (n = 7, 294 colonies counted) CLP populations. Values were determined by scoring pre–B cell colonies per 500 cells cultured. P values were determined by Student t test.

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