Figure 4
Figure 4. c-FLIPf/f LysM-Cre mice lack marginal zone macrophages and have splenomegaly and splenic extramedullary hematopoiesis. (A) Spleen weight (left) and cellularity of spleens lysed of red blood cells (right) in c-FLIPf/f and c-FLIPf/f LysM-Cre mice. Black boxes represent c-FLIPf/f mice and white boxes represent c-FLIPf/f LysM-Cre mice. Data were obtained in 5 independent experiments (spleen weights) or 7 independent experiments (splenic cellularity). **P < .01; ***P < .001. (B) Loss of CD115+ ER-TR9+ marginal zone macrophages but not MOMA-1+ metallophilic macrophages as observed by immunofluorescent staining. Frozen spleen sections from c-FLIPf/f (left) and c-FLIPf/f LysM-Cre (right) mice were stained for CD115 (red) and B220 (green; top), or MOMA-1 (blue) and ER-TR9 (green; bottom). Original magnifications 100× (top), 200× (bottom). Images were obtained using a Zeiss Axiovert 200M (10×/0.30 NA objective lens, top; 20×/0.75 NA objective lens, bottom) with an AxioCam MRm camera and AxioVision Rel. 4.8 software. (C) Images of paraffin-embedded spleen sections from c-FLIPf/f and c-FLIPf/f LysM-Cre mice stained with H&E. Original magnification 100×. Inset, image showing megakaryocytes in the spleen of a c-FLIPf/f LysM-Cre mouse. Original magnification 400×. Images were obtained using a Zeiss Axiovert 200 (10×/0.25 NA objective lens or 40×/0.50 NA objective lens, inset) with an AxioCam MRC camera and AxioVision Rel. 4.8 software. (D) Absolute numbers of CD4+ or CD8+ T cells, B220+ B cells, CD11b+ Ly6Cint neutrophils, and total SSClo cells (left) or SSClo CD11b+ Ly6Chi inflammatory monocytes and SSClo CD11b+ Ly6Clo resident monocytes (right) in c-FLIPf/f and c-FLIPf/f LysM-Cre spleens as determined by flow cytometry. Data were obtained in 4-7 independent experiments (T cells, 5 experiments; B cells, 4 experiments; neutrophils and monocytes, 6 experiments, and SSClo cells, 7 experiments). n = 7-14; NS, not significant; ***P < .001. (E-G) Absolute numbers of progenitor cells in spleen as determined by flow cytometry. Data were obtained in 2 independent experiments. n = 4; *P < .05; **P < .01. (E) Absolute numbers of Lin− (CD3ϵ−CD4−CD8−CD11b−B220−) cells. (F) Absolute numbers of LSK (Lin−Sca-1+c-Kit+) cells, CMP (Lin−c-Kit+Sca-1− CD34+ FcγRlo), and GMP (Lin−c-Kit+Sca-1− CD34+ FcγRhi) populations. (G) Absolute numbers of MEP (Lin− c-Kit+ Sca-1− CD34− FcγRlo) cells. In all panels, black bars represent c-FLIPf/f mice and white bars represent c-FLIPf/f LysM-Cre mice. *P < .05; **P < .01; ***P < .001. Error bars represent standard deviations.

c-FLIPf/f LysM-Cre mice lack marginal zone macrophages and have splenomegaly and splenic extramedullary hematopoiesis. (A) Spleen weight (left) and cellularity of spleens lysed of red blood cells (right) in c-FLIPf/f and c-FLIPf/f LysM-Cre mice. Black boxes represent c-FLIPf/f mice and white boxes represent c-FLIPf/f LysM-Cre mice. Data were obtained in 5 independent experiments (spleen weights) or 7 independent experiments (splenic cellularity). **P < .01; ***P < .001. (B) Loss of CD115+ ER-TR9+ marginal zone macrophages but not MOMA-1+ metallophilic macrophages as observed by immunofluorescent staining. Frozen spleen sections from c-FLIPf/f (left) and c-FLIPf/f LysM-Cre (right) mice were stained for CD115 (red) and B220 (green; top), or MOMA-1 (blue) and ER-TR9 (green; bottom). Original magnifications 100× (top), 200× (bottom). Images were obtained using a Zeiss Axiovert 200M (10×/0.30 NA objective lens, top; 20×/0.75 NA objective lens, bottom) with an AxioCam MRm camera and AxioVision Rel. 4.8 software. (C) Images of paraffin-embedded spleen sections from c-FLIPf/f and c-FLIPf/f LysM-Cre mice stained with H&E. Original magnification 100×. Inset, image showing megakaryocytes in the spleen of a c-FLIPf/f LysM-Cre mouse. Original magnification 400×. Images were obtained using a Zeiss Axiovert 200 (10×/0.25 NA objective lens or 40×/0.50 NA objective lens, inset) with an AxioCam MRC camera and AxioVision Rel. 4.8 software. (D) Absolute numbers of CD4+ or CD8+ T cells, B220+ B cells, CD11b+ Ly6Cint neutrophils, and total SSClo cells (left) or SSClo CD11b+ Ly6Chi inflammatory monocytes and SSClo CD11b+ Ly6Clo resident monocytes (right) in c-FLIPf/f and c-FLIPf/f LysM-Cre spleens as determined by flow cytometry. Data were obtained in 4-7 independent experiments (T cells, 5 experiments; B cells, 4 experiments; neutrophils and monocytes, 6 experiments, and SSClo cells, 7 experiments). n = 7-14; NS, not significant; ***P < .001. (E-G) Absolute numbers of progenitor cells in spleen as determined by flow cytometry. Data were obtained in 2 independent experiments. n = 4; *P < .05; **P < .01. (E) Absolute numbers of Lin (CD3ϵCD4CD8CD11bB220) cells. (F) Absolute numbers of LSK (LinSca-1+c-Kit+) cells, CMP (Linc-Kit+Sca-1 CD34+ FcγRlo), and GMP (Linc-Kit+Sca-1 CD34+ FcγRhi) populations. (G) Absolute numbers of MEP (Lin c-Kit+ Sca-1 CD34 FcγRlo) cells. In all panels, black bars represent c-FLIPf/f mice and white bars represent c-FLIPf/f LysM-Cre mice. *P < .05; **P < .01; ***P < .001. Error bars represent standard deviations.

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