Skip to main content
. Author manuscript; available in PMC: 2015 Apr 15.
Published in final edited form as: Sci Transl Med. 2015 Feb 18;7(275):275ra20. doi: 10.1126/scitranslmed.aaa1065

Fig. 4. Col IV–Ac2-26 NPs exert atheroprotective actions in myeloid-derived cells in an FPR2/ALX-dependent manner.

Fig. 4

Ldlr−/− mice were transplanted with bone marrow from WT or Fpr2−/− bone marrow. (A) Aortic root sections were stained with hematoxylin and eosin (H&E) (left), and cap thickness was quantified (right). Scale bar, 100 μm. (B) Collagenase activity was quantified in aortic root sections using fluorescence microscopy and image processing. (C) Superoxide (DHE) was assessed by fluorescence microscopy. Data are for individual mice, with means shown as horizontal lines (n = 5 separate mice, two sections per mouse). **P < 0.01 versus all other groups, one-way ANOVA with post hoc Tukey analysis.