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. Author manuscript; available in PMC: 2017 May 24.
Published in final edited form as: Nature. 2016 Nov 9;539(7630):575–578. doi: 10.1038/nature20170

Extended Data Figure 8. FAT1 suppresses proliferation and mitochondrial respiration in human SMCs.

Extended Data Figure 8

a, Western blotting for FAT1 expression in human aortic SMCs (HASMCs) treated with control siRNA (sictl) or FAT1 siRNAs (siFAT1) 1–3. For subsequent experiments, siFAT1 3 was used unless otherwise indicated. b, Proliferation of HASMCs after siFAT1 treatment, expressed as the ratio of EdU to Hoechst signal, normalized to sictl. n = 3, significance assessed by two-tailed t-test. c, Expression of cyclin D1 in sictl- or siFAT1-treated HASMCs. d, Oxygen consumption rate (OCR) of sictl- or siFAT1-treated HASMCs at baseline and in response to 2 µg ml−1 oligomycin (1), 3 µM FCCP (2), and 2 µM rotenone (3). e, Quantification of OCR from (d). n = 3, significance assessed by two-way ANOVA. All data shown as mean ± s.e.m. For gel source data, see Supplementary Fig. 1.