Figure 3
Altered localization of the stem/progenitor cells (cKitpos) within the architecture of the marrow of Gata1low mice. (A) Genomic organization of the murine Gata1 locus indicating the position of the proximal (IE) and distal (IT) promoter and of the HS1 (also known as HS-3.5 and G1HE), the HS2, and the HS4/5 (also known as HS+3.5) enhancer. The shaded box indicates the sequences deleted by the hypomorphic Gata1low mutation. The sequences −2.7 Kb upstream and 1.5 Kb downstream of IE driving the expression of the GFP reporter (−2.7Kb Gata1GFP) are indicated at the bottom (see also Skoda15 and Onodera et al25). (B-C) Double cKit and GFP immunofluorescence analysis of marrow and spleen sections of −2.7KbGata1GPFGata1+/0 (B) and −2.7KbGata1GPFGata1low/0 (C) mice, as indicated. The panels on the top present the merged pictures of representative areas of the bone marrow and spleen at ×20 magnification. The rectangles indicate the areas of the sections shown at higher (×40) magnification on the panels in the bottom. These bottom panels present the fluorescent signal of cKit and GFP captured individually and merged. The arrows track the position of individual cKitpos cells in the different panels. The red arrowhead in panel E indicates a GFPneg MK in proximity to the bone endosteum of the Gata1low mouse. Legend: −2.7KbGata1GPFGata1+/0 mouse: (i) 3 cKitposGFPneg cells, one of which is close to the endosteum; (ii) a cluster of cKitposGFPneg cells in the medulla; (iii) a cluster of cKitposGFPpos cells in the medulla; (iv) a cluster of cKitposGFPpos cells in the spleen. −2.7Kbgata1GPFGata1low/0 mouse: (v) a cluster of cKitposGFPpos cells close to the bone endosteum; (vi) a cluster of cKitposGFPneg cells in the medulla; (vii) a cluster of cKitposGFPpos cells in the spleen.

Altered localization of the stem/progenitor cells (cKitpos) within the architecture of the marrow of Gata1low mice. (A) Genomic organization of the murine Gata1 locus indicating the position of the proximal (IE) and distal (IT) promoter and of the HS1 (also known as HS-3.5 and G1HE), the HS2, and the HS4/5 (also known as HS+3.5) enhancer. The shaded box indicates the sequences deleted by the hypomorphic Gata1low mutation. The sequences −2.7 Kb upstream and 1.5 Kb downstream of IE driving the expression of the GFP reporter (−2.7Kb Gata1GFP) are indicated at the bottom (see also Skoda15  and Onodera et al25 ). (B-C) Double cKit and GFP immunofluorescence analysis of marrow and spleen sections of −2.7KbGata1GPFGata1+/0 (B) and −2.7KbGata1GPFGata1low/0 (C) mice, as indicated. The panels on the top present the merged pictures of representative areas of the bone marrow and spleen at ×20 magnification. The rectangles indicate the areas of the sections shown at higher (×40) magnification on the panels in the bottom. These bottom panels present the fluorescent signal of cKit and GFP captured individually and merged. The arrows track the position of individual cKitpos cells in the different panels. The red arrowhead in panel E indicates a GFPneg MK in proximity to the bone endosteum of the Gata1low mouse. Legend: −2.7KbGata1GPFGata1+/0 mouse: (i) 3 cKitposGFPneg cells, one of which is close to the endosteum; (ii) a cluster of cKitposGFPneg cells in the medulla; (iii) a cluster of cKitposGFPpos cells in the medulla; (iv) a cluster of cKitposGFPpos cells in the spleen. −2.7Kbgata1GPFGata1low/0 mouse: (v) a cluster of cKitposGFPpos cells close to the bone endosteum; (vi) a cluster of cKitposGFPneg cells in the medulla; (vii) a cluster of cKitposGFPpos cells in the spleen.

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