Figure 1.
Cebpa enhancer deletion causes neutropenia and reduction in LT-HSCs of +37kbHOM BMs. (A-B) Representative flow cytometry plots showing Mac1+Gr1+ myeloid cell populations in PB (A) and BM (B) of +37kbWT (blue), +37kbHET (green), and +37kbHOM (red) mice. (C) Absolute numbers of Mac1+Gr1+ cells calculated from total PB counts of 37kbWT (blue), +37kbHET (green), and +37kbHOM (red) mice. (D) Relative numbers of total Mac1+Gr1+ cells calculated from total BM cell count from 1 femur, corrected for body weight in grams of each mouse. (E) Hematoxylin and eosin (H&E) staining of representative cross sections showing BM architecture (left), identifying megakaryocytes (right [arrows]) in +37kbWT and +37kbHOM mice. (F) S100A8 immunohistochemical staining of representative BM cross sections from 37kbWTand +37kbHOM mice. (G) Representative flow cytometry plots of LK, LSK, LT-HSC, ST-HSC, MPP3, MPP2 cell populations in BM of 37kbWT, +37kbHET, and +37kbHOM mice. (H) Absolute numbers of CD150+CD48- LT-HSCs calculated from total BM cell counts from 1 femur. All data are represented as mean +/− SD. Statistical significance was calculated using a Student t-test. *P value < .05; **P value < .005; ***P value < .0005; N.S., not significant; SD, standard deviation; LK, Lineage- cKit+; LSK, Lineage- Sca1+ cKit+; LT-HSC, long-term hematopoietic stem cell; ST-HSC, short-term hematopoietic stem cell; MPP, multipotent progenitor; +37kbWT, wild type +37kb enhancer; +37kbHET, heterozygous +37kb enhancer deletion; +37kbHOM, homozygous +37kb enhancer deletion.

Cebpa enhancer deletion causes neutropenia and reduction in LT-HSCs of +37kbHOM BMs. (A-B) Representative flow cytometry plots showing Mac1+Gr1+ myeloid cell populations in PB (A) and BM (B) of +37kbWT (blue), +37kbHET (green), and +37kbHOM (red) mice. (C) Absolute numbers of Mac1+Gr1+ cells calculated from total PB counts of 37kbWT (blue), +37kbHET (green), and +37kbHOM (red) mice. (D) Relative numbers of total Mac1+Gr1+ cells calculated from total BM cell count from 1 femur, corrected for body weight in grams of each mouse. (E) Hematoxylin and eosin (H&E) staining of representative cross sections showing BM architecture (left), identifying megakaryocytes (right [arrows]) in +37kbWT and +37kbHOM mice. (F) S100A8 immunohistochemical staining of representative BM cross sections from 37kbWTand +37kbHOM mice. (G) Representative flow cytometry plots of LK, LSK, LT-HSC, ST-HSC, MPP3, MPP2 cell populations in BM of 37kbWT, +37kbHET, and +37kbHOM mice. (H) Absolute numbers of CD150+CD48- LT-HSCs calculated from total BM cell counts from 1 femur. All data are represented as mean +/− SD. Statistical significance was calculated using a Student t-test. *P value < .05; **P value < .005; ***P value < .0005; N.S., not significant; SD, standard deviation; LK, Lineage- cKit+; LSK, Lineage- Sca1+ cKit+; LT-HSC, long-term hematopoietic stem cell; ST-HSC, short-term hematopoietic stem cell; MPP, multipotent progenitor; +37kbWT, wild type +37kb enhancer; +37kbHET, heterozygous +37kb enhancer deletion; +37kbHOM, homozygous +37kb enhancer deletion.

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