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. 2013 Feb 15;123(3):1323–1334. doi: 10.1172/JCI63891

Figure 3. Depletion of Tregs affects cellular composition of atheroma.

Figure 3

(A) Representative fluorescence micrographs depicting eGFP+FOXP3+ cells (arrowheads) and eGFPFOXP3+ (arrows) cells in aortic lesions of DEREG/Ldlr–/– mice treated for 8 weeks with PBS or DT. Anti-GFP was labeled with AlexaFluor 488 (green), anti-FOXP3 with AlexaFluor 555 (red), and nuclei with DAPI (blue). (B) Quantitation of immunohistochemical staining for T cells (CD3+), Tregs (FOXP3+), and I-Ab–expressing (MHCII-expressing) cells (all expressed as stained cells per lesion area) in the proximal aorta of chimeric DEREG/Ldlr–/– mice treated for 8 weeks with DT or PBS; n = 7–8 mice per group. (C) Quantitation of immunohistochemical staining for macrophages (CD68+), dendritic cells (CD11c+), and expression of the adhesion molecule VCAM-1 (all expressed as stained area per lesion area) in the aortic sinus of chimeric DEREG/Ldlr–/– mice treated for 8 weeks with DT or PBS; n = 7–8 mice per group. (D) Cellularity of atherosclerotic lesions (DAPI+ nuclei per lesion area) in the proximal aorta of chimeric DEREG/Ldlr–/– mice treated for 8 weeks with PBS or DT; n = 7–8 mice per group. (E) Necrotic core area relative to total atherosclerotic lesion area in the proximal aorta of chimeric DEREG/Ldlr–/– mice treated for 8 weeks with PBS or DT; n = 7–8 mice per group. *P < 0.05; **P < 0.01. Scale bars: 50 μm.