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. 2012 Feb 1;122(2):783. doi: 10.1172/JCI62827

Genetic inactivation of IL-1 signaling enhances atherosclerotic plaque instability and reduces outward vessel remodeling in advanced atherosclerosis in mice

Matthew R Alexander, Christopher W Moehle, Jason L Johnson, Zhengyu Yang, Jae K Lee, Christopher L Jackson, Gary K Owens
PMCID: PMC3266814

Original citation: J. Clin. Invest. 2012;122(1):70–79. doi:10.1172/JCI43713.

Citation for this erratum: J. Clin. Invest. 2012;122(2):783. doi:10.1172/JCI62827.

During the preparation of this manuscript, errors were inadvertently introduced into the legends for Figures 1, 2, and 3. The correct sections of the legends appear below.

Figure 1: (B) Quantification of total atherosclerotic plaque area within the aortic root of Il1r1+/+Apoe–/– and Il1r1–/–Apoe–/– mice at 150-μm intervals from the aortic valve attachment site (P < 0.001 for difference between genotypes by Scheirer-Ray-Hare test). n = 13, Il1r1+/+Apoe–/–; n = 12, Il1r1–/–Apoe–/–. Data represent mean ± SEM.

Figure 2: L-1R1 deficiency reduces compensatory outward remodeling of atherosclerotic brachiocephalic arteries. (A) Movat staining of representative brachiocephalic arteries of Il1r1–/–Apoe–/– and Il1r1+/+Apoe–/– mice. Scale bars: 200 μm. (BD) Atherosclerotic plaque area (B), vessel area within the IEL (P < 0.001 for difference between genotypes by 2-way ANOVA) (C), and lumen area (P < 0.001 for difference between genotypes by 2-way ANOVA after square root transformation) (D) at multiple locations along the brachiocephalic arteries of Il1r1–/–Apoe–/– and Il1r1+/+Apoe–/– mice. n = 14, Il1r1+/+Apoe–/–; n = 12, Il1r1–/–Apoe–/–. Data in BD represent mean ± SEM.

Figure 3: (FJ) Quantification of (F) plaque collagen content based on picrosirius red staining, P < 0.001 for difference of genotypes by 2-way ANOVA, (G) plaque SMC coverage based on SM α-actin staining, P < 0.001 for difference of genotypes by the Scheirer-Ray-Hare test, (H) total plaque SMC content based on SM α-actin staining, P < 0.001 for difference of genotypes by the Scheirer-Ray-Hare test, (I) plaque macrophage content based on Mac2 staining, P = 0.01 for difference of genotypes by 2-way ANOVA after log transformation, and (J) the percentage of brachiocephalic arteries exhibiting intraplaque hemorrhage based on Movat and TER-119 staining, **P < 0.01 by Fisher’s exact test.

The JCI regrets the error.


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