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. Author manuscript; available in PMC: 2014 May 10.
Published in final edited form as: Sci Transl Med. 2013 Aug 28;5(200):200ra117. doi: 10.1126/scitranslmed.3006674

Fig. 2. Increased macrophage LTA4H over time in developing PH.

Fig. 2

(A to D) Representative immunofluorescence images from lung sections stained with antibody to LTA4H (green) and CD68 (red) from (A) DMSO, (B) 1 week after SU, (C) 2 weeks after SU, and (D) 3 weeks after SU. DAPI (blue) identifies nuclei. Green arrows point to the center of occluded arterioles. Merged panel shows all three stains. (E)Quantitation of LTA4H staining over time in PH in pulmonary macrophages. LTA4H+, CD68+ macrophages were counted per high-power field. (F) LTA4H mRNA, as measured by RT-PCR. (G) p5-LO+ or LTA4H+ macrophages were counted and grouped as <50 µm, 50 to 100 µm, or 100 to 150 µm from the center of the small pulmonary arterioles. n = 6 per group. Scale bar, 50 µm. Kruskal-Wallis test followed by Dunn’s multiple comparisons test for post hoc analyses was used. Data are means ± SEM.