Figure 4.
Figure 4. Intrafollicular emergence of bone marrow–derived leukocytes. (A) Vibrissal follicles isolated from the chimeric mice reconstituted with EGFP+ bone marrow cells were cultured for 3 weeks in the presence of 5 added growth factors and examined under confocal microscopy. The displayed images represent multiple clusters of EGFP+ cells detected in 2 different planes within the same HF sample (left and middle panels) and extrafollicular expansion of EGFP+ cells on the top of EGFP– fibroblasts observed on the plane corresponding to the surface of culture plates (right panel). (B) Vibrissal follicles freshly isolated from the chimeric mice reconstituted with EGFP+ bone marrow cells were examined under confocal microscopy. The images show 3 vertical planes (with the follicular papilla side at the bottom) of a representative HF sample scanned sequentially with 5 μm distance between planes. The ORS regions delineated by their faint autofluorescence signals are outlined by dotted lines. Data shown are representative of 3 (A) or 2 (B) independent experiments. Scale bars represent 50 μm (A) or 100 μm (B).

Intrafollicular emergence of bone marrow–derived leukocytes. (A) Vibrissal follicles isolated from the chimeric mice reconstituted with EGFP+ bone marrow cells were cultured for 3 weeks in the presence of 5 added growth factors and examined under confocal microscopy. The displayed images represent multiple clusters of EGFP+ cells detected in 2 different planes within the same HF sample (left and middle panels) and extrafollicular expansion of EGFP+ cells on the top of EGFP fibroblasts observed on the plane corresponding to the surface of culture plates (right panel). (B) Vibrissal follicles freshly isolated from the chimeric mice reconstituted with EGFP+ bone marrow cells were examined under confocal microscopy. The images show 3 vertical planes (with the follicular papilla side at the bottom) of a representative HF sample scanned sequentially with 5 μm distance between planes. The ORS regions delineated by their faint autofluorescence signals are outlined by dotted lines. Data shown are representative of 3 (A) or 2 (B) independent experiments. Scale bars represent 50 μm (A) or 100 μm (B).

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